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Parenting

Recall: More Than 500,000 Diono Children’s Car Seats

1:45

Diono has announced that it is recalling more than 500,000 car seats after concerns that they may not adequately protect children in a crash. The recall covers the following models: Radian R100, Radian R120, Radian RXT, Olympia, Pacifica and Rainier convertible and booster seats. The car seats were made from as early as January 2014 to September 2017 by Diono, which used to be called Sunshine Kids Juvenile.

The U.S. National Highway Traffic Safety Administration says that when the seats are secured using a lap belt without the top tether, children over 65 pounds have an increased risk of chest injury in a crash.

Diono, based in Sumner, Washington, says it has no reports of injuries and that few children who weigh more than 65 pounds will be harnessed into the seats. The problem was discovered in company testing. The company will send owners a kit with an energy absorbing pad and a new chest clip at no cost. The recall is expected to start November 22. Customers with questions can call Diono at (855) 463-4666.

Consumers can also click on https://us.diono.com/safety-notice/ for more information.

To ensure that your child is using the car seat safest for them Rachel Rothman, Chief Technologist in the Good Housekeeping Institute, recommends taking the following precautions:

  • Buy a car seat that is age and size appropriate. Resist the urge to deviate from this so you can better see your child or for other reasons.
  • Make sure that when installing a car seat the latch straps or seatbelt straps are not twisted.
  • A properly installed car seat should not move more than one inch from side to side and front to back.
  • Read the car seat instruction manual as well as the vehicle owner manual for proper installation instructions.
  • Check the return policy on your car seat before you make a purchase in case you buy the wrong size and need to replace it.
  • Delay switching to front-facing car seats as late as possible to ensure safety. Before you make the switch, make sure your child truly has outgrown their current seat.

Story source: http://www.goodhousekeeping.com/travel-products/car-seat-reviews/news/a46498/diono-car-seat-recall/

https://us.diono.com/safety-notice/

Your Toddler

Ikea Recalls 29 Million Chests and Dressers After More Children Die

2:00

The U.S. Consumer Product Safety Commission (CPSC), in cooperation with IKEA North America, of Conshohocken, Pa., is announcing the recall of all chests and dressers that do not comply with the performance requirements of the U.S. voluntary industry standard (ASTM F2057-14).  The recalled children’s chests and dressers are taller than 23.5 inches and adult chests and dressers are taller than 29.5 inches.  The 29 million units of recalled chests and dressers include: MALM 3-drawer, 4-drawer, 5-drawer and three 6-drawer models and other children’s and adult chests and dressers.  The recalled chests and dressers are unstable if they are not properly anchored to the wall, posing a serious tip-over and entrapment hazard that can result in death or serious injuries to children.

 On July 22, 2015, CPSC and IKEA announced a repair program for the chests and dressers that included a free wall-anchoring repair kit for the MALM chests and dressers and other IKEA chests and dressers. Two tragic fatalities involving MALM chests and dressers occurred prior to the announcement of the repair program:

·      In February 2014, a 2-year-old boy from West Chester, Pa. died after a 6-drawer MALM chest tipped over and fatally pinned him against his bed.

·      In June 2014, a 23-month-old boy from Snohomish, Wash. died after he became trapped beneath a 3-drawer MALM chest that tipped over. 

Subsequent to the July 2015 announcement, CPSC and IKEA learned of additional tip-over incidents, including a February 2016 incident in which a 22-month-old boy from Apple Valley, Minn. died when a MALM 6-drawer chest fell on top of him. 

 None of the chests or dressers in the above-listed incidents had been anchored to the wall.  In addition to the three deaths, IKEA received reports of 41 tip-over incidents involving the MALM chests and dressers, resulting in 17 injuries to children between the ages of 19 months and 10 years old.

 The MALM chests and dressers are constructed of particleboard or fiberboard and are white, birch (veneer), medium brown, black-brown, white stained oak (veneer), oak (veneer), pink, turquoise, grey, grey-turquoise, lilac, green, brown stained ash (veneer), and black.  A 5-digit supplier number, 4-digit date stamp, IKEA logo, country of origin and “MALM” are printed on the underside of the top panel or inside the side panel. 

 Since 1996, IKEA chests and dressers have been labeled to identify IKEA, the model name and the manufacturing date.

 The recalled MALM chests were sold from 2002 through June 2016 for between $70 and $200. 

 Recalled MALM Chest and Drawers:

·      MALM 3 – Sold 10/2002 to 6/2016

·      MALM 4 – Sold 6/2002 to 6/2016

·      MALM 5 -  Sold 10/2002 to 4/2006

·      MALM 6-  Sold 6/2002 to 6/2016

·      MALM 6 LONG – Sold 11/2002 to 6/2016

·      MALM 6 – Sold 4/2006 to 6/2016

IKEA also received 41 reports of tip-overs involving chests and dressers other than MALMs, resulting in the deaths of three children and 19 injuries to children:

·      In July 1989, a 20-month-old girl from Mt. Vernon, Va. died after  an unanchored GUTE 4-drawer chest tipped over and pinned her against the footboard of a youth bed.

·      In March 2002, a 2½-year-old boy from Cranford, N.J. died after an unanchored RAKKE 5-drawer chest tipped over and fatally pinned him to the floor.

·      In October 2007, a 3-year-old girl from Chula Vista, Calif. died after a KURS 3-drawer chest tipped over and fatally pinned her to the floor.  It is unknown as to whether the dresser was anchored or not.

Other recalled Chest and Drawers:

Most of the non-MALM chests and dressers included in this recall are listed on the IKEA website at www.IKEA-USA.com/recallchestsanddressers.

 Since 1996, IKEA chests and dressers have been labeled to identify IKEA, the model name and the manufacturing date.

 CPSC and IKEA are urging consumers to inspect their recalled IKEA chests and dressers to ensure that they are properly anchored to the wall.  Chests and dressers should be properly anchored to the wall whether or not they meet the ASTM standard.  Consumers should move any unanchored chests and dressers into storage or other areas where they cannot be accessed by children until the chests and dressers are properly anchored to the wall or removed from the home.

To receive a refund or free wall-anchoring kit for IKEA chests and dressers listed above, visit an IKEA retail store, go to www.IKEA-USA.com/recallchestsanddressers , or call 866-856-4532 anytime.

A child dies every two weeks and a child is injured every 24 minutes in the U.S. from furniture or TVs tipping over, according to CPSC data.

Remedy

Consumers should immediately stop using any recalled chest and dresser that is not properly anchored to the wall and place it into an area that children cannot access.  Contact IKEA for a choice between two options: refund or a free wall-anchoring repair kit.

Consumers are entitled to a full refund for chests and dressers manufactured between January 2002 and June 2016. Consumers with chests and dressers manufactured prior to January 2002 will be eligible for a partial store credit. 

Consumers can order a free wall-anchoring repair kit. Consumers can install the kit themselves or IKEA will provide a one-time, free in-home installation service, upon request. Consumers can reorder the kits throughout the life of their chest and dresser.

Story Source: http://www.cpsc.gov/en/Recalls/2016/IKEA-Recalls-29-Million-MALM-and-Other-Models-of-Chests-and-Dressers/

 

 

Daily Dose

Teething Pain & Recalled OTC Products

Do OTC teething products really work? Which ones have been recalled? WHat parents need to know.I am getting a lot of questions from patients related to teething, pain, and the recall of over the counter teething products that contain benzocaine.

The FDA recently issued a warning to parents who use OTC products like Oragel and Anbesol on their infant’s gums for relief of teething pain. These products come as both liquids and gels, and benzocaine is the active pain reducing ingredient. It has now been found that excessive amounts of benzocaine may lead to a very rare, condition called methemoglobinemia. (Hemoglobin is the molecule in the red blood cell that carries oxygen). With methemoglobinemia there is a reduced amount of oxygen that is carried in the bloodstream which may lead to a bluish gray discoloration to the skin, shortness of breath, a rapid heart rate and fatigue and lethargy. Although the FDA did not withdraw these products from the market, they did recommend that they not be used in children under two, and then should be used “sparingly”. Unfortunately, the benzocaine containing products do not yet contain warning labels. I have never recommended using these products in the first place. I always wondered if they really helped a baby who was teething, as I am not sure you can tell when a baby is teething in the first place. If you watch any infant over the age of 4 months, their hands are always in their mouths, and they are constantly drooling!  Does that mean they are getting teeth? Unlikely, as most babies don’t even cut their first tooth until about 6 months, so they have been drooling and putting anything they can in their mouths for months prior. The drooling and “gnawing” on their hands (and sometimes feet too) is rather a developmental milestone and not always a sign of teething. My theory is let the baby chew on a teething ring, a frozen piece of a bagel (cut into quarters, good for gnawing and can throw out when used), or rub their gums with a cold washcloth if you think your child has discomfort. Babies will get teeth for many years to come and once the first several have broken the skin we don’t seem to pay as much attention anyway, right?  I mean, who is going to worry about a child cutting their 2 year old molars, there are way too many other issues to deal with (tantrums, climbing, throwing food) than if their molars are erupting. So, save your money and don’t buy teething products. Now the FDA even agrees! What do you think? I look forward to your feedback.

Your Baby

Recall: 86,000 Osprey Poco Child Backpack Carriers

1:30

Osprey Child Safety Products is recalling 82,000 Poco child carriers after receiving reports that children have fallen from the seats.

Osprey has received four reports of children falling through the carrier leg openings, resulting in one report of a skull fracture and one report of scratches to the head.

This recall involves all models of Poco, Poco Plus and Poco Premium child backpack carriers manufactured between January 2012 and December 2014.  The nylon child carriers were sold in three colors: “Romper Red,” “Koala Grey,” and “Bouncing Blue.” They have a metal frame and a gray padded child’s seat inside. The production date is stamped on a black label sewn into the interior of the large lower zippered compartment on the back of the carrier.

Recalled carriers have a production date code of S12SBPR1, S12SBPR1B, S12SBPR2, S12SBPR3, S12SBPR4, F12SBPR1, F12SBPR2, S13SB IPO, S13SBPR1, S13SBPR2, S13SBPR3, S13SBPR4, F13SBPR1, F13SBPR2, F13SBPR3, S14SBPR1, S14SBPR2, S14SBPR3, S14SBPR4, S14SBPR5. “Osprey” is printed on the fabric above the kickstand. The model name is printed on the back at the bottom.

Consumers should immediately stop using the recalled carriers and contact Osprey for a free Seat Pad Insert for use along with the existing safety straps to secure the child in the carrier. Consumers who previously received and installed the free Seat Pad Insert in their carriers are not required to take further action.

The child carriers were sold at REI and specialty outdoor stores nationwide and online at Amazon.com from January 2012 to December 2015 for between $200 and $300. 

Consumers can contact Osprey, toll-free ,at 866-951-5197 from 8 a.m. to 5 p.m. MT Monday through Friday, email at pocoseatpad@ospreypacks.com or online at www.ospreypacks.com and click on “Poco Safety Notices” on the navigation bar at the top right hand corner of the page for more information.

Story source: https://www.cpsc.gov/Recalls/2017/osprey-recalls-child-backpack-carriers#

Your Toddler

Safety 1st Recalls Décor Wood Highchairs Due to Falls

1:30

Dorel Juvenile Group, of Columbus, Ind., is recalling about 35,000 Safety 1st Wood Décor highchairs because a child can remove the highchair’s tray, posing a fall hazard.

Safety 1st has received 68 reports of children removing the trays and 11 reports of injuries such as lacerations, chipped teeth and bruises.

The highchairs were sold at Babies R US and Toys R Us retail stores nationwide and online at www.Amazon.com, www.BabiesRUs.com, www.ToysRUs.com and www.Walmart.com and other online retailers from May 2013 through May 2015 for about $120.

This recall includes Safety 1st Wood Décor highchairs in three models: HC144BZF (Casablanca), HC229CZF (Gentle Lace) and HC229CYG (Black Lace). The model numbers are printed under the highchair seat. These A-frame black wood highchairs have a removable fabric, black and white print seat pad with a blue or pink border on the top and bottom of the seat pad. The highchairs have a white plastic, detachable tray with a cone-shaped center divider that fits between a child’s legs. “Safety 1st” is printed on the front center of the tray.

Consumers should immediately stop using these recalled highchairs and contact the firm to receive instructions on receiving a new tray with labels.   

Consumers can contact Safety 1st toll-free at (877) 717-7823 from 8 a.m. to 5 p.m. ET Monday through Friday, email at decorwoodhighchair@djgusa.com or online at www.safety1st.com and click on “Safety Notices” at the top of the page for more information.

Source: http://www.cpsc.gov/en/Recalls/2016/Safety-1st-Recalls-Decor-Wood-Highchair/

 

Your Toddler

Recall Reminder: 8th Child Dies From Fallen IKEA Dresser

2:00

IKEA has voluntarily issued a reminder about its recall of MALM and other models of chests and dressers due to a serious tip-over hazard. An 8th child has reportedly died after being trapped under a fallen IKEA dresser.

CEO Lars Petersson said Ikea wants to increase awareness of the recall campaign for several types of chest and dressers that can easily tip over if not properly anchored to a wall.

The initial recall was issued in June 2016, for 17.3 million chests and drawers. The Swedish retailer and the federal safety regulators are reminding customers to take immediate action to secure the dressers, or to return them.

This recall re-announcement involves MALM and other IKEA chests and dressers that do not comply with the requirements of the U.S. voluntary industry standard (ASTM F2057-14).  The recalled children’s and adult chests and dressers include the MALM 3-drawer, 4-drawer, 5-drawer and three 6-drawer models and other non-MALM models.  The recalled children’s chests and dressers are taller than 23.5 inches; recalled adult chests and dressers are taller than 29.5 inches. 

The MALM chests and dressers are constructed of particleboard or fiberboard and are white, birch (veneer), medium brown, black-brown, white stained oak (veneer), oak (veneer), pink, turquoise, grey, grey-turquoise, lilac, green, brown stained ash (veneer), and black.  A 5-digit supplier number, 4-digit date stamp, IKEA logo, country of origin and “MALM” are printed on the underside of the top panel or inside the side panel.  

To see a complete list of other non-MALM chests and dressers included in this recall, click on this link www.IKEA-USA.com or http://www.ikea.com/ms/en_US/ikea-chest-and-dresser-recall/index.htmlon IKEA’s website.

Dangerous tip-over incidents often occur when curious kids climb on furniture in an attempt to access TVs, toys, remotes or other desired items.  While the threat is serious, the solution is simple. Anchor TVs, furniture and appliances in the home. And when product recalls are announced, act on them immediately. Visit AnchorIt.gov to see how TV and furniture tip-over incidents occur and the simple steps to prevent them.

Story Source: https://www.cpsc.gov/Recalls/2018/IKEA-Reannounces-Recall-of-MALM-and-Other-Models-of-Chests-and-Dressers-Due-to-Serious-Tip-over-Hazard

Your Child

McDonald’s Recalls Kid's “Step-iT” Wristbands Due to Burns, Skin Irritations

1:30

About 29 million of McDonald’s “Step-iT” activity wristbands have been recalled in the U.S. due to skin irritations or burns to children.

The recall involves “Step-iT” activity wristbands, which come in two styles—“Activity Counter” and a motion-activated “Light-up Band.” The Activity Counter comes in translucent plastic orange, blue or green and features a digital screen that tracks a child’s steps or other movement. The Light-up Band comes in translucent plastic red, purple, or orange and blinks light with the child’s movement. Both styles of activity wristbands have a square face with the words “STEP-iT” printed on them and a button to depress and activate the wristband. The back of the square face contains the etched words “Made for McDonald’s.” 

The company has received more than 70 reports of incidents, including seven reports of blisters, after wearing the wristbands.

Consumers should immediately take the recalled wristbands from children and return them to any McDonald’s for a free replacement toy and either a yogurt tube or bag of apple slices.

The wristbands were distributed exclusively by McDonald’s restaurants nationwide, from August 9, 2016 to August 17, 2016 with Happy Meals and Mighty Kids Meals. 

Consumers can contact McDonald’s at 800-244-6227 from 7 a.m. to 7 p.m. CT daily, or online at www.mcdonalds.com and click on “Safety Recall” for more information. 

You can see all the models recalled on http://www.cpsc.gov/en/Recalls/2016/McDonalds-Recalls-Step-iT-Activity-Wristbands/

Daily Dose

Rotarix Vaccine Temporarily Suspended

The FDA suspends Glaxo Rotarix vaccine I received the CDC Health Alert yesterday afternoon notifying physicians to “temporarily suspend the usage of GlaxoSmithKline (GSK) Rotarix (rotavirus) vaccine. Rotarix was licensed for use in 2008 to prevent rotavirus disease, which typically causes fever, vomiting and diarrhea in infants and young children.

Prior to this Merck’s vaccine RotaTeq had been licensed for us in 2006. Both of these vaccines are given orally. Both RotaTeq and Rotarix were found to prevent serious rotavirus illness and hospitalizations for dehydration. The GSK product, Rotarix, which is a “live attenuated” vaccine, has been found to contain DNA from porcine circovirus type 1 (PCV 1). PCV 1 virus is not known to multiply in human cells or to cause illness.  According to the FDA, “all available evidence indicates that there had been no increased risk to patients who have received this vaccine”.  The GSK vaccine, Rotarix, is made in a different manner than the Merck vaccine RotaTeq.  Preliminary studies by the FDA on RotaTeq vaccine have not shown the presence of PCV 1 DNA. Preliminary data reported to the FDA  by GSK related to PCV 1 being in the vaccine seems to suggest that it has been present since the early stages of the vaccine’s development.  Studies on Rotarix, both before and after the approval of the vaccine, have shown it to be extremely safe and no unusual adverse events have been reported.  At the same time, the vaccines that have been given are presumed to be effective. In the interim, while futher studies are being completed, it is recommended that children continue to receive RotaTeq vaccine.  The FDA plans to convene an advisory committee to look into how the DNA components came to be present in this vaccine. They are also going to look into the use of new techniques for identifying viruses in vaccines.  After this meeting, the FDA will make further recommendations about the use of rotavirus vaccines in the United States. This recall was limited to the United States, and children in other areas or the world are continuing to receive Rotarix, as the available evidence suggests that the benefits of the vaccine outweigh the risks, especially in areas where rotavirus disease causes severe disease and even deaths. I would not be alarmed if my baby had received this vaccine as it does not cause disease in animals or humans.  I would also complete my child’s vaccine series with the Merck product which is available.  We will all have to stay tuned for further details,  but this should also make parents aware that the safety of vaccines continues to be monitored, even after they have been approved. That's your daily dose for today.  We'll chat again tomorrow! Send Dr. Sue your question now!

Parenting

Cashews Recalled Due to Glass Pieces

1:30

Nuts have become a go-to snack for many families looking to live a healthier life. If you’ve purchased cashews from an ALDI grocery store recently, be sure to check and see if the brand is Southern Grove Cashew Halves and Pieces with Sea Salt.

The recall was initiated after the company received consumer reports of glass found in the product. To date, there have not been any reported injuries. Potentially impacted product has been removed from store shelves.

This recall affects the Southern Grove Cashew Halves and Pieces with Sea Salt sold in 8-ounce (227-gram) canisters, labeled with UPC No. 041498179366. The affected cashews have best by dates of 11/27/18 and 11/28/18.

The cashews were sold by ALDI stores in 29 states: Alabama, Arkansas, California, Florida, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Maryland, Michigan, Minnesota, Mississippi, Missouri, Nebraska, New York, North Carolina, Ohio, Oklahoma, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Virginia, Washington, D.C., West Virginia, and Wisconsin.

Consumers who have purchased the product in question are urged not to consume this product and may return the product to their local ALDI store for a refund or dispose of the item.

Consumers with questions may contact Star Snacks at 201-882-4593 or RecallFEQ01@gmail.com, Monday-Friday 9 am – 2 pm EST.

Story source: https://www.fda.gov/Safety/Recalls/ucm562129.htm

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