Baby and kids' product recalls
6672 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.
- 2018-12-05FDA-FoodRed Bull North America Inc.Class IIIRed Bull Energy Drink, 8.4 Fl. oz. (250 mL) Ingredient: Carbonated water, Sucrose, Glucose, Citric Acid, Taurine, Sodium Bicarbonate, Magnesium, Carbonate Caffeine, Nicainamide, Calcium Pantothenate, Pyridoxine HCL, Vitamin B12, Natural and artificial Flavors, colors. UPC CODES: 6 11269 99100 0 (ON THE CANS) AND 61126991246 (ON THE CASES) distributed by Red Bull, N.A. Inc., Santa Monica, CA Made in Austria.
Investigation of complaints of off taste color and taste found that the product contained 3 times the level of the primary ingredients than is specified in the product formulation.
- 2018-11-28FDA-DeviceGE Healthcare, LLCClass IIPanda Wall Mount warmer. Infant radiant warmer
Potential electric leakage affecting the user.
- 2018-11-28FDA-DeviceGE Healthcare, LLCClass IIPanda Freestanding Warmer. Device sold under the following product names: Panda Freestanding Warmer and Panda Freestanding Warmer Generic ATO Model. Infant Radiant warmer.
Potential electric leakage affecting the user.
- 2018-11-28FDA-DeviceGE Healthcare, LLCClass IIPanda iRes Infant Radiant Warmer. Device sold under the following product names: Panda iRes Warmer and Panda iRes Bedded Warmer.
Potential electric leakage affecting the user.
- 2018-11-28FDA-DeviceGE Healthcare, LLCClass IIGiraffe Warmer. Device sold under the following product names: Giraffe Warmer and Giraffe Bedded Warmer. infant radiant warmer.
Potential electric leakage affecting the user.
- 2018-11-28FDA-DrugEcolab IncClass IIMedi-Stat Foam, Antimicrobial Hand Soap, Chloroxylenol 0.5%, 1250 mL (42.3 fl oz), OTC, Ecolab, 370 Wabasha Street N, St. Paul, MN 55102, NDC 47593-503-59
Labeling: Label mix-up - the label on the product may not match the formula in the bottle.
- 2018-11-28FDA-DrugEcolab IncClass IIEqui-Soft Foam, Antimicrobial Hand Soap, 0.55% Benzalkonium Chloride, 25 fl oz (750 mL), OTC, Ecolab, 370 Wabasha Street N, St. Paul, MN 55102, NDC 47593-521-41
Labeling: Label mix-up - the label on the product may not match the formula in the bottle.
- 2018-11-27CPSCZhejiang Focus-On Import & Export, of Binjiang District, ChinaLumber Liquidators Recalls 5-Gallon Buckets Due to Drowning Hazard (Recall Alert)
Young children can fall into buckets and drown. The buckets do not have the required cautionary label warning of the drowning risk posed to young children.
- 2018-11-21FDA-DrugTaro Pharmaceuticals U.S.A., Inc.Class IIchildren's allergy relief (cetirizine hydrochloride) oral solution, 1 mg/mL, Dye Free, Sugar Free, Alcohol Free, 4 FL OZ (120 mL) bottle, Distributed by Rite-Aid, 30 Hunter Lane, Camp Hill, PA 17011, Made in Israel, UPC 0 11822 57363 4.
Failed Impurities/Degradation Specifications: unknown impurity higher than the specified limit was detected during routine stability testing.
- 2018-11-21FDA-DrugTaro Pharmaceuticals U.S.A., Inc.Class IIchildren's allergy (cetirizine hydrochloride) Oral Solution, 1 mg/mL, ANTIHISTAMINE, Dye-Free, Sugar-Free, 4 FL OZ (120 mL) bottle, Distributed by Publix Super Markets, Inc., 3300 Publix Corporate Parkway, Lakeland, FL 33811, NDC 56062-106-08, UPC 0 41415 43573 5.
Failed Impurities/Degradation Specifications: unknown impurity higher than the specified limit was detected during routine stability testing.
- 2018-11-21FDA-DrugTaro Pharmaceuticals U.S.A., Inc.Class IIChildren's 24 Hour Allergy (cetirizine hydrochloride) Oral Solution 1 mg/mL, Bubble Gum Flavor, Sugar Free/Dye Free, 4 FL OZ (120 mL) bottle, Dist. by Meijer Distribution, Inc., Grand Rapids, MI 40644, NDC 41250-106-08, UPC 7 13733 88578 2.
Failed Impurities/Degradation Specifications: unknown impurity higher than the specified limit was detected during routine stability testing.
- 2018-11-20CPSCG & Y Company Limited, of Hong KongHoMedics Recalls Nightlights Due to Choking Hazard (Recall Alert)
The small feet on the giraffe-shaped nightlight can detach, posing a choking hazard to small children.
- 2018-11-15CPSCHeritage Creations, of Gurgaon, IndiaRH Recalls Metal-Wrapped Coffee Tables Due to Risk of Lead Exposure (Recall Alert)
The tables' metal top can contain lead and presents a risk of lead exposure to children. Lead is toxic if ingested and can cause adverse health effects.
- 2018-11-15CPSCLÍLLÉbaby, LLC, of Golden, Colo.LÍLLÉbaby Recalls Baby Carriers Due to Fall Hazard (Recall Alert)
The sliding chest-clip strap can detach from the shoulder strap, posing a fall hazard to the child in the carrier.
- 2018-11-14FDA-DeviceQiagen Sciences LLCClass IIEZ1 Advanced XL, Model Number: 9001492, GTIN: 04053228010760 Product Usage: The EZ1 Advanced XL is designed to perform automated isolation and purification of nucleic acids. It is intended to be used only in combination with QIAGEN kits indicated for use with the EZ1 Advanced XL instrument for the applications described in the kit handbooks. The system is intended for use by professional users, such as technicians and physicians trained in molecular biological techniques and the operation of
An issue with the power branching printed circuit board (PCB) on the instrument that has the potential to trigger a heater malfunction was discovered. If this failure were to occur, nucleic acid extractions could be compromised and extractions need to be repeated. This could cause a delay in obtaining results from downstream applications.
- 2018-11-08CPSCNingbo Younker Fashion Accessory Industrial Corporation, of ChinaH.I.S. Recalls Girl's Clothing Sets Due to Violation of Federal Lead Content Ban
The metal pendant on the necklace contains levels of lead that exceed the federal lead content ban. Lead is toxic if ingested by young children and can cause adverse health issues.
- 2018-11-08CPSCDayu Household Products Company, of ChinaMountain Warehouse Recalls Children's Water Bottles Due to Choking Hazard
The water bottle's spout can detach, exposing a small ring, posing a choking hazard to children.
- 2018-11-07NHTSA-EquipmentKidde Technologies, Inc.Kidde Technologies, Inc. — Fire Suppression System May Not Discharge
If the fire suppression system does not work as intended, it can increase the risk of injury in the event of a fire.
- 2018-11-01CPSCRidge Properties, DBA Pain Relief Naturally, of Salem, Ore.Pain Relief Naturally Recalls Pain and Itch Relief Creams, Sprays and Gels Due to Failure to Meet Child Resistant Closure Requirement; Risk of Poisoning (Recall Alert)
The packaging is not child resistant as required by the Poison Prevention Packaging Act. The pain and itch relief creams, sprays and gels contain lidocaine, posing a risk of poisoning to young children if they put it on their skin or ingest it.
- 2018-10-31FDA-DeviceCustom Healthcare Systems, Inc.Class IICHS Custom Convenience Kit-FORMULA CAP (10'S Product Number: UNC-9538
Convenience kits were sealed in immediate Tyvek pouches using incorrect specifications compromising product sterility
- 2018-10-31FDA-DrugWestlab Pharmacy, Inc. dba Westlab PharmacyClass IIAlprostadil 500 mcg/mL Injectable, Vials, Westlab Pharmacy, Inc., Gainesville, FL 32607 NDC 10002-7335-00
Incorrect Product Formulation
- 2018-10-31FDA-DrugValeant Pharmaceuticals North America LLCClass IICortaid 12-Hour Advanced Anti-itch Cream (1% hydrocortisone), NET WT 1.5 oz. (42 g) tube, OTC, Distributed by: Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807, UPC code 301875519155
CGMP deviations: Notice received from supplier of a voluntary recall of all their nasal products and baby oral gels due to the possibility of microbial contamination. No positive results for the firm's products. were obtained. After the firm review, cGMP deviations ere evident.
- 2018-10-31FDA-DrugValeant Pharmaceuticals North America LLCClass IICortaid Maximum Strength Cream (1% hydrocortisone), 1 OZ (28 g) tube, OTC, Distributed by: Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807, UPC code 301875521011
CGMP deviations: Notice received from supplier of a voluntary recall of all their nasal products and baby oral gels due to the possibility of microbial contamination. No positive results for the firm's products. were obtained. After the firm review, cGMP deviations ere evident.
- 2018-10-31FDA-DrugValeant Pharmaceuticals North America LLCClass IICortaid Intensive Therapy Cooling Spray (1% hydrocortisone), 2 FL OZ (59 mL) spray bottle, OTC, Distributed by: Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807, UPC code 301875518028
CGMP deviations: Notice received from supplier of a voluntary recall of all their nasal products and baby oral gels due to the possibility of microbial contamination. No positive results for the firm's products. were obtained. After the firm review, cGMP deviations ere evident.
- 2018-10-31CPSCYumark Enterprises Corp/Yumark Pacific LTD., of ChinaFantasia Accessories Recalls Slap Bracelets Due to Laceration Hazard; Sold Exclusively at Target
The slap bracelet's metal wristband can pierce the protective fabric around it and expose sharp edges, posing a laceration hazard to young children.
- 2018-10-26CPSCCreative Sto, of ChinaChildren's Toy Instrument Sets Recalled Due to Violation of the Federal Lead Paint Ban; Made by Creative Sto and Sold Exclusively at Amazon.com (Recall Alert)
Paint on the maracas, xylophone and carrying case 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.
- 2018-10-25CPSCGogo Toys Co. LTD, of Taiwani play Recalls Infant Rattles Due to Choking Hazard
Pieces of the rattle can detach, posing a choking hazard to infants.
- 2018-10-24FDA-DevicePhilips Electronics North America Corp.Class IIPhilips HeartStart FR3 Defibrillator, Model: 861388, 861389 Product Usage: The HeartStart FR3 is used to treat suspected victims of ventricular fibrillation (VF), the most common cause of sudden cardiac arrest (SCA), and certain ventricular tachycardia (VTs). Both models are used with disposable pads applied to potential victims of SCA with the following symptoms: 1) Unresponsiveness 2) Absence of normal breathing The HeartStart FR3 is intended for adults and children over 55 pounds (25kg) o
Automated external defibrillators may not fully meet IPx5 water ingress specification. The device may fail to function should water intrusion occur.
- 2018-10-24FDA-DrugProduct Quest Manufacturing LLCClass IIFinafta Baby, Oral Gel (benzocaine 7.5%), 7.1 Grams (0.25 Oz.) tube, Distributed By: Efficient Laboratories, Inc., Miami, FL 33166.
CGMP Deviations: products manufactured under conditions that could impact its product quality.
- 2018-10-24FDA-DrugProduct Quest Manufacturing LLCClass IICVS Health, Saline Nasal Gel with Soothing Aloe, packaged as a) Baby Net Wt. 0.5 OZ (14.2 g) tube UPC 0 50428 58392 0 Product #282476; and b) Net Wt. 0.5 OZ tube (14.2 g) UPC 0 50428 31746 4 Product #896071; Distributed by CVS Pharmacy, Inc,. One CVS Drive, Woonsocket, RI 02895.
CGMP Deviations: products manufactured under conditions that could impact its product quality.
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