Baby and kids' product recalls
6719 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.
- 2021-04-15USDAClass IThrow out Olymel Celebrity imported ham
Product Contamination
- 2021-04-14FDA-DeviceBecton Dickinson & Co.Class IIBD BBL Martin-Lewis Agar 20 Ea - Product Usage: use for the isolation of pathogenic Neisseria from specimens containing mixed flora of bacteria and fungi. Catalog Number: 221557
Products show heavy growth of C. albicans after 24 hours of incubation due to misformulation (expected reaction is partial inhibition after 18-48 hours incubation) and reduce the identification of Neisseria contributing to a delay in time to definitive diagnosis or a delay in proper treatment
- 2021-04-14FDA-DeviceBecton Dickinson & Co.Class IIBD BBL Martin-Lewis Agar, 100 Ea - Product Usage: used for the isolation of pathogenic Neisseria from specimens containing mixed flora of bacteria and fungi. Catalog Number: 221558
Products show heavy growth of C. albicans after 24 hours of incubation due to misformulation (expected reaction is partial inhibition after 18-48 hours incubation) and reduce the identification of Neisseria contributing to a delay in time to definitive diagnosis or a delay in proper treatment
- 2021-04-14FDA-FoodCanteen Inc. dba MG Foods, Inc.Class IMG Foods THE CLUB SUB ROAST BEEF, TURKEY, HAM & BABY SWISS WITH GOLDEN ITALIAN DRESSING ON MULTI-GRAIN BATARD, Net Wt. 8.5oz (242g), MG Foods Charlotte, NC 28208, UPC 1 00000 50002 6
The firm received positive test results for Listeria monocytogenes during in house environmental sampling on one of their meat slicers.
- 2021-04-14FDA-DrugAlembic Pharmaceuticals LimitedClass ITelmisartan Tablets, USP 20 mg, 30-count bottles, Rx only, Manufactured by: Alembic Pharmaceuticals Limited (Formulation Division) Panelav 38935, Gujarat, India Manufactured for: Alembic Pharmaceuticals, Inc. 750 Route 202, Bridgewater, NJ 08807, NDC 62332-087-30
Labeling: Label-mixup
- 2021-04-14CPSCPlaygro USA LLC, of Whittier, Calif.Playgro Recalls Infant Activity Rattles Due to Choking Hazard
The abacus ring on the horses back can dislodge and release the small beads, posing a choking hazard to small children.
- 2021-04-14CPSCTarget Corp., of Minneapolis, Minn.Target Recalls Cat & Jack Baby Rompers Due to Choking Hazard
The heart-shaped graphics located on the knees of the romper can peel off or detach, posing a choking hazard to children.
- 2021-04-14CPSCTarget Corporation, of Minneapolis, Minn.Battat Recalls Infant Teethers Due to Choking Hazard; Sold Exclusively at Target
The plastic wings can detach from the body of the teether, posing a choking hazard to young children.
- 2021-04-10USDAPublic Health AlertThrow out recalled Plainville ground turkey products
Product Contamination
- 2021-04-08CPSCGeo Essential LLC, of Orem, UtahGEO Essential Recalls Wintergreen Organic Essential Oil and Alleviate Organic Essential Oil Blend Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
These products contain the substance methyl salicylate, which must be in child resistant packaging, as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant, posing a risk of poisoning if the contents are swallowed by young children.
- 2021-04-07FDA-DeviceCovidien LlcClass IIBRAVO PH CAPS DELIVERY DEV5-PK, FGS-0312/FGS-0313 - Product Usage: intended to be used for gastroesophageal pH measurement and monitoring of gastric reflux in adults and children from 4 years of age.
The capsule may fail to attach to the esophageal mucosa, which in turn may lead to the aspiration of the capsule. In the event of capsule aspiration, immediate intervention to remove the capsule is required. Potential outcomes following capsule aspiration include low oxygen saturation, intervention to retrieve the capsule, potential need to intubate the patient, extended hospital stay and a delay of treatment. Thirteen reports of capsule aspiration have been received the last 2 years.
- 2021-04-07FDA-DeviceCovidien LlcClass IICF Delivery Dev Caps Bravo x5, FGS-0635/FGS 0636 - Product Usage: intended to be used for gastroesophageal pH measurement and monitoring of gastric reflux in adults and children from 4 years of age.
The capsule may fail to attach to the esophageal mucosa, which in turn may lead to the aspiration of the capsule. In the event of capsule aspiration, immediate intervention to remove the capsule is required. Potential outcomes following capsule aspiration include low oxygen saturation, intervention to retrieve the capsule, potential need to intubate the patient, extended hospital stay and a delay of treatment. Thirteen reports of capsule aspiration have been received the last 2 years.
- 2021-04-07FDA-FoodAMPIClass IIAMPI Buttermilk Powder, formula 219. 25 KG Net (55.12 Lbs Net). Distributed by: Associated Milk Producers, Inc., New Ulm, Minnesota 56073. Packaged in Kraft Paper Poly-lined bags.
The Buttermik powder may contain a Foreign Material (metal).
- 2021-04-07CPSCRH US LLC, of Corte Madera, Calif.RH Recalls Children's Bath Wraps Due to Violation of Federal Flammability Standard
The recalled bath wraps fail to meet flammability standards for children's sleepwear, posing a risk of burn injuries to children.
- 2021-04-01CPSCDONGGUAN BABYCARE PRODUCTS CO., LTD, of Dongguan, ChinaInfant Bath Seats Recalled Due to Drowning Hazard; Imported by BATTOP; Sold Exclusively on Amazon.com (Recall Alert)
The bath seats fail to meet the federal safety standard for infant bath seats, including requirements for stability, and can tip over while in use, posing a drowning hazard to babies.
- 2021-04-01CPSCdoTERRA International LLC, of Pleasant Grove, UtahdoTERRA Recalls 1.3 Million Bottles of Deep Blue, PastTense, and Deep Blue Touch Essential Oils Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
The products contain the substance methyl salicylate, which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant, posing a risk of poisoning if the contents are applied to the skin or swallowed by young children.
- 2021-03-24FDA-DeviceMedtronic Perfusion SystemsClass IMedtronic Custom Pack Infant Tubingset Pixie Flow 0,8->1,5-1,8 1/B (PERFUSION M483203D 1/B). The Affinity Pixie Cardiotomy/Venous Reservoir (CVR) with Balance Biosurface is a single-use device designed to collect and store blood during extracorporeal circulation. Cardiotomy blood is collected, filtered, and defoamed before mixing with the venous blood, which is filtered. The primary blood-contacting surfaces of the CVR are coated with Balance Biosurface to reduce platelet activation and ad
Products being recalled due to potentially elevated level of bacterial endotoxin. Patients exposed to elevated levels of bacterial endotoxins may develop an acute inflammatory response.
- 2021-03-24FDA-FoodMinnesota Milk Bank for BabiesClass IIIMN Milk Bank for Babies Pasteurized Donor Human Milk. Volumne 4.0 fl oz., 120 mL
Pasteurized donor human milk may contain trace amounts of dextromethorphan.
- 2021-03-24NHTSA-EquipmentDionoDiono — Headrest May Break or Separate/FMVSS 213
A broken or separated headrest increases the risk of injury during a crash.
- 2021-03-18CPSCGenentech, a member of the Roche Group, of South San Francisco, Calif.Genentech Recalls Prescription Drug Evrysdi Due to Failure to Meet Child Resistant Packaging Requirements; Risk of Drug Exposure through Eye or Skin Absorption (Recall Alert)
The bottles containing the prescription drug can leak due to a fit issue between the press-in bottle adapter and bottleneck. If the bottle is leaking, there is a risk of drug exposure by contact with skin or eyes. Prescription drugs must be in child resistant packaging that prevents children from gaining access to the contents as required by the Poison Prevention Packaging Act (PPPA).
- 2021-03-17FDA-DeviceSunstar Americas, Inc.Class IISUNSTAR G.U.M. HYDRAL DRY MOUTH RELIEF On-the-go Oral Spray, 2 FL.OZ. UPC0 70942 30713 0 - Product Usage: The device is formulated with water, moisturizers /humectants including one plant-based moisture rich humectant, sweeteners and flavors that collectively have lubricating, moisturizing, soothing, and refreshing properties to help relieve and manage the symptoms of dry mouth.
The product may be contaminated with Burkholderia cepacia
- 2021-03-08NHTSA-EquipmentCombi USA, Inc.Combi USA, Inc. — Child Seat Webbing May Fail/FMVSS 213
A child that is not adequately restrained in a crash has an increased risk of injury.
- 2021-03-04CPSCCasa Collection Design Group Inc., of Brooklyn, N.Y.Casa Kids Recalls for Repair Cabina Bunk Beds Due to Fall Hazard (Recall Alert)
The screws that hold the bed's mattress foundation to the bed's guardrails can be loose and the mattress foundation can fall, posing a fall risk to children in the bunk bed.
- 2021-02-25CPSCMTIG Productions LLC, dba deSensua, of Buffalo, Wyo.MTIG Productions Recalls deSensua Wintergreen, Birch and Pain Soother Essential Oils Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
The products contain the substance methyl salicylate which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant, posing a risk of poisoning if the contents are swallowed by young children.
- 2021-02-25CPSCDr. Reddy's Laboratories, Ltd., of IndiaDr. Reddy's Recalls Prescription Drug Blister Packages Due to Risk of Poisoning
The products are prescription medications that were labeled and distributed by Dr. Reddy's for institutional use only. The prescription medications were distributed by third party wholesalers to retail pharmacies and could have been dispensed to consumers. The packaging of the products is not child resistant and can pose a risk of poisoning if the contents are swallowed by young children.
- 2021-02-24CPSCShenzhen Haochen Industrial Co. Ltd., of ChinaSmartPool Recalls Children's Multi-Purpose Helmets Due to Risk of Head Injury
The recalled helmets were incorrectly advertised and marketed for children aged 2 years or older. However, the recalled helmets do not comply with minimum safety requirements for children younger than 5 and pose a risk of head injury to those children.
- 2021-02-17FDA-FoodOcean Beauty Seafoods LLCClass IIThe RETAIL package is black cardboard box and product is described as: Publix Parmesan-Crusted Wild Alaskan Salmon Fillets, Frozen, net wt. 12 oz. Each retail box has 2 individually vacuum-packaged portions of 5oz salmon with 1oz of glaze of soy sauce for each portion. The salmon and glaze are both in a vacuum-packed twin saddle clear pack. Product of USA. Distributed by Publix Super Markets, Inc. Lakeland, FL. UPC 41415 30245 7. The MASTER case (at warehouse and retail store level) is desc
Undeclared Soy
- 2021-02-17CPSCAnker Play Products, of Miami, FlaAnker Play Products Recalls 10-in-1 Incredible Inventions Science Kit Due to Violation of the Federal Lead Paint Ban
Paint on the red and blue magnet contains levels of lead that exceed the federal lead paint ban. Lead is toxic if ingested by young children and can cause adverse health issues. In addition, the product packaging lacks the required warning labels for magnets and balloons.
- 2021-02-10FDA-DeviceSmith & Nephew, Inc.Class IIVERSABOND AB 40 GRAMS FORMULATION 2, antibiotic infused bone cement, Product Number: 71271440 - Product Usage: VERSABOND is a medium viscosity bone cement which can be used for hip, knee, and shoulder implant fixation. VERSABOND AB includes the antibiotic- gentamycin.
Potential heat and humidity exposure. The affected lot contained an atypical sandy, flaky or grainy consistency when mixing.
- 2021-02-03FDA-DeviceQiagen Sciences LLCClass IItherascreen PIK3CA RGQ PCR Kit (23) US IVD product- aid clinicians in identifying breast cancer patients who may be eligible for treatment with PIQRAY (alpelisib) based on a PIK3CA Mutation Detected result. REF 873121
Kit may generate false Q546R mutation positive results caused by nonspecific molecular interactions within the Q546R higher than previously observed and described within the Instructions For Use.
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