Baby and kids' product recalls
6673 federal recalls on file. Every federal recall touching baby and kids' products — toys, formula, baby food, cribs, strollers, child seats. Sourced from CPSC, FDA, USDA, and NHTSA, translated into plain English.
- 2015-03-18FDA-FoodAbbott LaboratoriesClass IISimilac¿ Advance Complete Nutrition Infant Formula with Iron, 1.45lb plastic container.
The firm received three consumer calls of product with Chinese labeling. After an internal investigation, the firm discovered that product manufactured for export to China was distributed to three states in the US. All labeling is in Chinese.
- 2015-03-18NHTSA-EquipmentGraco Children's Products, Inc.Graco Children's Products, Inc. — Label Missing Instruction Manual Information
If the label does not inform the seat owner of the instruction manual's location, the owner may not be able to refer to it and may use the seat improperly, increasing the risk of injury to the child in the event of a crash.
- 2015-03-14USDAClass IICheck your freezer for Gourmet Kitchen beef and chicken products
Misbranding, Unreported Allergens
- 2015-03-12CPSCLevels of Discovery, of Overland Park, KansasLevels of Discovery Recalls Airplane Rocker Due to Choking Hazard (Recall Alert)
The red wooden knobs on the rocker's steering panel console can detach, posing a small parts choking hazard to young children.
- 2015-03-12CPSCMars Retail Group, of Mount Arlington, N.J.Youth Loungewear Pants Recalled by M&M'S World Store Due to Violation of Federal Flammability Standard
The youth loungewear pants fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injury to children.
- 2015-03-11FDA-DeviceBaxter Healthcare Corp.Class IIAMIA v1.0 APD System. For Automated Peritoneal Dialysis (APD) therapy for pediatric and adult renal patients.
Additional warning in the AMIA APD System labeling for patients vulnerable to unintended Increased Intraperitoneal Volume (IIPV), also known as overfill. The patients include neonates, infants, small children, and any patient with significant heart and/or lung disease.
- 2015-03-11CPSCFred Meyer, Inc., of Portland, Ore. dba Kroger of Cincinnati, OhioKid's Korner Children's Zipper Hooded Sweatshirts Recalled by Kroger Due to Choking Hazard
The sweatshirt zipper pull can detach, posing a choking hazard to young children.
- 2015-03-10CPSCK.J. Sportswear California Inc., of Huntington Beach, Calif.Children's Pajamas Recalled by K.J. Sportswear California Due to Violation of Federal Flammability Standard
The pajamas fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injury to children.
- 2015-03-04CPSCKTM North America, Inc., of Amherst, OhioChildren's Pajamas Recalled by KTM North America for Violation of Federal Flammability Standard
The pajamas fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries to children.
- 2015-03-03CPSCShanghai Daafu Baby, of ChinaDream on Me Recalls 2-in-1 Bassinet to Cradle Due to Fall and Suffocation Hazards
The wire supports on the sides of the bassinet can disconnect causing the fabric sides to lower; posing a risk that infants can fall out or become entrapped and suffocate.
- 2015-03-03CPSCFlow Sports Inc., of San Clemente, Calif.Flow Sports Inc. Recalls Snowboard Bindings Due to Fall Hazard
A pin can disengage and cause the binding to open, posing a fall hazard.
- 2015-03-02USDAClass IIDon't eat H-E-B cheese burgers; wheat allergen unlabeled
Misbranding, Unreported Allergens
- 2015-02-25FDA-DeviceAlivecor SFOClass IIIAlive ECG App 2.1.2 ( a medical device application for the Apple iOS operating system, intended to be used with the AliveCor Heart Monitor. The AliveCor Heart Monitor is intended to record, store and transfer single-channel electrocardiogram (ECG) rhythms. The AliveCor Heart Monitor also displays ECG rhythms and detects the presence of atrial fibrillation and normal sinus rhythm (when prescribed or used under the care of a physician).
Alive ECG App version 2.1.2 (intended to be used with the AliveCor Heart Monitor) crashed upon use of the application.
- 2015-02-12CPSCWalter Kidde Portable Equipment Company Inc., of Mebane, North CarolinaKidde Recalls Disposable Plastic Fire Extinguishers Due to Failure to Discharge
A faulty valve component can cause the disposable fire extinguishers not to fully discharge when the lever is repeatedly pressed and released during a fire emergency, posing a risk of injury.
- 2015-02-11FDA-DeviceCardinal HealthClass IILubricated Intubating Stylet 6FR that is inserted into an endotracheal tube to facilitate intubation. This product is used in surgical or medical emergency facilities. Primarily used on infants and pediatric patients.
A small piece of the stylet sheath has the potential to shear off upon removal of the stylet from the tracheal tube.
- 2015-02-11FDA-DrugTaro Pharmaceuticals U.S.A., Inc.Class IIChildren's Loratadine Syrup (Loratadine Oral Solution) 5 mg/5 mL, Antihistamine, Grape Flavored Syrup, 24 Hour Non-Drowsy Allergy Relief Sugar Free, 4 FL OZ (120 mL) Bottles, Distributed by: Taro Pharmaceuticals U.S.A., Inc. Hawthorne, NY 10532. NDC: 51672-2092-8.
Presence of Foreign Substance: Presence of blue plastic floating in loratadine syrup.
- 2015-02-10CPSCMarin Mountain Bikes Inc., of Novato, Calif.Marin Mountain Bikes Recalls Children's Bicycles Due to Fall Hazard; Handlebars Can Loosen
The handlebars can loosen or separate during use. This can cause the rider to lose control and/or crash, posing the risk of injury.
- 2015-02-05CPSCSparklegate Industries, of Dongguan, Guangdong, China, through a contract manufacturing relationship with Mima International Limited, of Hong KongMima Recalls Moon 3-In-1 High Chairs Due to Fall and Impact Hazard
The high chair seat can loosen and dislodge, allowing the seat and child to fall. The chair can also fall onto a child crawling underneath the seat, posing an impact hazard to the child.
- 2015-02-05CPSCLS Import, of Houston, TexasAirplane and Butterfly Push Toys Recalled by LS Import Due to Choking Hazard
The wheels of the airplane and the balls at the tip of the butterfly's antenna can detach, posing a choking hazard to young children.
- 2015-02-04FDA-FoodSunBurst Foods, Inc.Class IHam & Swiss on Sourdough w/Baby Carrots, Net. Wt. 10.30 oz., UPC 7-01248-00957-1, MFG Code 1666
Listeria monocytogenes
- 2015-02-04FDA-FoodSunBurst Foods, Inc.Class IBBQ Chicken on 100% Wheat Roll w/Baby Carrots, Net Wt. 7.80 oz., UPC 7-01248-010775-5, MFG Code 1792
Listeria monocytogenes
- 2015-02-04CPSCLazy One, Inc., of North Logan, UtahChildren's Pajamas and Robes Recalled by Lazy One Due to Violation of Federal Flammability Standard
The footed pajamas and robes fail to meet the federal flammability standard for children's sleepwear, posing a burn hazard to children.
- 2015-02-03CPSCPerformance Packaging, of Las Vegas, NevadaPerformance Packaging Recalls Children's Food Pouch Attachment Due to Choking Hazard
The tube of the pouch topper that screws onto the food pouch can separate from the round base, posing a choking hazard to young children.
- 2015-01-30USDAClass IDon't eat recalled cooked pork products
Misbranding, Unreported Allergens
- 2015-01-30USDAClass IStop consuming Hatfield Smokey Chipotle ribs
Misbranding, Unreported Allergens
- 2015-01-28USDAClass IDon't use Washington Beef trim product
Product Contamination
- 2015-01-21USDAClass IDon't eat Holiday Foods meat products
Misbranding, Unreported Allergens
- 2015-01-17USDAClass ICheck for Sabor Latino meat products with peanut allergen
Misbranding, Unreported Allergens
- 2015-01-14FDA-DeviceBaxter Healthcare Corp.Class IIHomeChoice Automated PD system and HomeChoice Pro Automated PD system Baxter's HomeChoice and HomeChoice Pro APD systems are designed to provide Automated Peritoneal Dialysis (APD) therapy for pediatric and adult renal patients. Their Fill volumes can range from 60 mL to 3000 mL. The HomeChoice and HomeChoice Pro APD systems are intended to be operated by: 1) Home patients whose physicians have prescribed this system. Patients, or their caregivers, must have received adequate training to use
There are additional and updated warning and cautions that are not in the Patient At-Home Guide for HomeChoice Automated PD Systems and HomeChoice PRO Automated PD Systems.
- 2015-01-14FDA-DeviceOrthovita, Inc., dBA Stryker Orthobiologics.Class IIStryker Orthobiologics Imbibe Bone Marrow Aspiration Needle, Model Numbers: 2090-0027 Needle (bullet-tip), 11 gauge x 4 inch 2090-0028 Needle (bullet-tip), 11 gauge x 6 inch 2090-0029 Needle (bullet-tip), 8 gauge x 6 inch 2090-0047 Needle (bullet-tip), 8 gauge x 8 inch 2090-0030 Needle (bullet-tip), Fenestrated, 8 gauge x 6 inch intended for use to aspirate bone marrow or autologous blood.
There is the potential for a breach in the inner or outer packaging pouches of all lots of the Imbibe Bone Marrow Aspiration Needle.
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