Baby and kids' product recalls
6675 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.
- 2014-04-30CPSCAvix Technology, TaiwanHorizon Hobby Recalls Blade 700 X Pro Series Helicopter Kits, Spindle Sets Due To Injury Hazard
The main rotor washer can fail, causing the blades to come off the helicopter during use. This poses an injury hazard to the operator and bystanders.
- 2014-04-29CPSCFXR Factory Racing Inc., Oak Bluff, Manitoba, CanadaFXR Factory Racing Recalls Children's Outerwear Due to Strangulation Hazard
Drawstrings can become entangled or caught on playground slides, hand rails, school bus doors or other moving objects, posing a significant strangulation and/or entanglement hazard to children.
- 2014-04-29CPSCIKEA North America, of Conshohocken, Pa.IKEA Reannounces and Expands Recall of Children's Wall-Mounted Lamps Due to Strangulation Hazard
Children can get entangled in the electrical cord that hangs from the children's wall-mounted lamps, posing a strangulation hazard.
- 2014-04-25USDAClass IIDo not eat Knockum Hill Bar-B-Que smoked pork
Misbranding, Unreported Allergens
- 2014-04-24CPSCRunway Global, of New York, N.Y.Runway Global Recalls Sugarfly Girls’ Coats; Waist Drawstring Poses Entanglement Hazard
The coats have a drawstring tie sewn into the side seam at the waist that could become snagged or caught in small spaces or vehicle doors, posing significant entanglement hazard to children.
- 2014-04-24USDAClass IDo not eat Cobblestone Farms pork ribs
Produced Without Benefit of Inspection
- 2014-04-23CPSCSummer Infant, of Woonsocket, R.I.Summer Infant Expands Recall to Replace Video Monitor Rechargeable Batteries Due to Burn Hazard
The battery in the handheld video monitor can overheat and rupture, posing a burn hazard to consumers.
- 2014-04-20USDAClass IStop using Oscar Mayer Classic Wieners
Misbranding, Unreported Allergens
- 2014-04-19USDAClass IDon't serve Sugar Lake Farms chicken breast products
Misbranding, Unreported Allergens
- 2014-04-16FDA-FoodNature's Value Inc.Class IIvitacost brand Men's Passion Booster, 30 Capsules, PREMIUM FORMULA DIETARY SUPPLEMENT, ITEM # NSI 3004713, UPC 8 35003 00471 3, and 120 CAPSULES, ITEM # NSI 3009473, UPC 8 35003 00947 3 --- Manufactured for Vitacost Lexington, NC 27295
The product was produced using bulk L-Citrulline lot # 121109 which was subsequently recalled by the supplier since the lot was found to contain a compound other than L-Citrulline.
- 2014-04-16FDA-DrugZions RX Formulations Services LLC dba RX Formuations Serv.Class IIVitamin B-12 injections, a) 1 mL and b) 30 mL units, Not for Dispensing, For Hospital Administration Only, Rx Formulations, 5949 East University Drive, Mesa, AZ 85205
Lack of Assurance of Sterility: The firm expanded the recall to other injectable products due to lack of assurance of sterility from poor aseptic practices observed at the firm.
- 2014-04-16FDA-DrugZions RX Formulations Services LLC dba RX Formuations Serv.Class IIBupivacaine 3%, 300 mL units, Not for Dispensing, For Hospital Administration Only, Rx Formulations, 5949 East University Drive, Mesa, AZ 85205
Lack of Assurance of Sterility: The firm expanded the recall to other injectable products due to lack of assurance of sterility from poor aseptic practices observed at the firm.
- 2014-04-16FDA-DrugZions RX Formulations Services LLC dba RX Formuations Serv.Class IISodium Bicarbonate 8.4%, a) 10 mL, b) 20 mL, and c) 22 mL units, Not for Dispensing, For Hospital Administration Only, Rx Formulations, 5949 East University Drive, Mesa, AZ 85205
Lack of Assurance of Sterility: The firm expanded the recall to other injectable products due to lack of assurance of sterility from poor aseptic practices observed at the firm.
- 2014-04-16FDA-DrugZions RX Formulations Services LLC dba RX Formuations Serv.Class IIOxytocin 30 Units in 500mL Sodium Chloride 0.9% Bags, Not for Dispensing, For Hospital Administration Only, Rx Formulations, 5949 East University Drive, Mesa, AZ 85205
Lack of Assurance of Sterility: The firm expanded the recall to other injectable products due to lack of assurance of sterility from poor aseptic practices observed at the firm.
- 2014-04-16FDA-DrugZions RX Formulations Services LLC dba RX Formuations Serv.Class IIPotassium Phosphates 4.4mEq/3mM/mL Vials, Not for Dispensing, For Hospital Administration Only, Rx Formulations, 5949 East University Drive, Mesa, AZ 85205
Lack of Assurance of Sterility: The firm expanded the recall to other injectable products due to lack of assurance of sterility from poor aseptic practices observed at the firm.
- 2014-04-16FDA-DrugZions RX Formulations Services LLC dba RX Formuations Serv.Class IIMagnesium Sulfate 10gm in 250mL Lactated Ringers Bags, Not For Dispensing, For Hospital Administration Only, Rx Formulations, 5949 East University Drive, Mesa, AZ 85205
Lack of Assurance of Sterility: The firm expanded the recall to other injectable products due to lack of assurance of sterility from poor aseptic practices observed at the firm.
- 2014-04-16FDA-DrugZions RX Formulations Services LLC dba RX Formuations Serv.Class ICalcium Gluconate 10% for Injection, SDV 100 mL SDV, PF, Not for Dispensing, For Hospital Administration Only, Rx Formulations, 5949 East University Drive, Mesa, AZ, 85205.
Non-Sterility: RX Formulation initiated this recall due to a report of microbial contamination found in Calcium Gluconate saturated solution that was observed upon drawing the vial contents into a syringe.
- 2014-04-10CPSCBedHead Pajamas Inc., of Los Angeles, Calif.BedHead Pajamas Recalls Children's Pajamas Due to 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.
- 2014-04-09FDA-DeviceAllesee Orthodontic AppliancesClass IIAOA Distalizer Lock Nut Screw, found in products listed as: Distal Jet, Spring Jet, Mesial Jet, and Uprighter Jet. Removable functional orthodontic appliances that are to modify the growth of the jaws in a prescribed growth pattern.
The Lock Nut component of the Jet appliances may be missing the screw collar, which serves as a mechanical stop to prevent over-tightening in appliance assemby. Without this collar, an over-tightened lock nut may stop the piston assembly from moving freely, subsequently preventing intended movement of the teeth.
- 2014-04-09FDA-DeviceInfantino LLCClass IIInfantino Squeeze & Teethe Monkey, "Go Gaga Squeeze & Teether Coco the Monkey". Non-Fluid Filled Teething Ring.
Infantino initiated this voluntary recall of all lots of Infantino Squeeze & Teethe Monkey, "Go Gaga Squeeze & Teethe Coco the Monkey", Model Number 206-647, because the tail of the monkey may pose a choking hazard to young children.
- 2014-04-09FDA-DeviceDraeger Medical Systems, Inc.Class IDraeger PS500 Power Supply Unit of the Infinity ACS Workstation Critical Care (Evita Infinity V500), Evita V500 and /or Babylog VN500 Ventilators, used for ventilation during short term transport of patients within a hospital.
The battery capacity of the optional PS500 Power Supply Unit of the Infinity ACS Workstation Critical Care (Evita Infinity V500) did not last as long as expected.
- 2014-04-09FDA-FoodButter Creek Farms, Inc.Class IMock Baby Ruth Cookies
Butter Creek Farms, Inc. is recalling Mock Baby Ruth Cookies due to undeclared peanut, egg, wheat, soy, wheat, and milk. The firm sold single product or combined this product with other products in gift boxes from the website http://cowchipcookies.com/index.htm.
- 2014-04-09FDA-FoodWinn-Dixie Logistics, Inc.Class IWinn-Dixie Chocolate Flavored Drink Mix NET WT 30 OZ (1 LB 14 OZ) 851 G Distributed by: Winn-Dixie Stores, Jacksonville, FL 32254
Product may contain incorrect formula mixture, which could result in an undeclared milk allergen.
- 2014-04-09CPSCJ.P. Boden Services, of Pittston, Pa.J.P. Boden Recalls Boys' Pajamas Due to Violation of Federal Flammability Standard (Recall Alert)
The pajamas fail to meet the federal flammability standards for children's sleepwear, posing a risk of burn injury to children.
- 2014-04-03NHTSA-EquipmentEvenflo Company, Inc.Evenflo Company, Inc. — Buckle may be difficult to Unlatch
It may be difficult to remove the child from the restraint, increasing the risk of injury in the event of an emergency in which a prompt exit from the vehicle is required.
- 2014-04-02FDA-FoodPlum IncClass IIStage 2 World Baby ; Zucchini & Spinach with Pasta Marinara; 3.5 oz. pouch. Product of USA distributed by Plum Inc., Emeryville, CA
Intermittent damage to the plastic spouts during manufacturing of two varieties of Plum products on two product dates may cause plastic fragments to break loose and cause a potential choking hazard.
- 2014-04-02FDA-FoodPlum IncClass IIStage 2 World Baby Thailand; Roasted Pumpkin & Coconut Rice, 3.5 oz. pouch. Product of USA distributed by Plum Inc., Emeryville, CA
Intermittent damage to the plastic spouts during manufacturing of two varieties of Plum products on two production dates may cause plastic fragments to break loose and cause a potential choking hazard.
- 2014-04-01NHTSA-EquipmentBaby Trend, Inc.Baby Trend, Inc. — Buckle may be difficult to unlatch
It may be difficult to remove the child from the restraint, increasing the risk of injury in the event of an emergency in which a prompt exit from the vehicle is required.
- 2014-03-26FDA-DevicePhilips Medical Systems North America Inc.Class IIPhilips HeartStart Home and OnSite (HS1) automated external defibrillators (AEDs). Product Usage: The models M5066A, M5067A, and M5068A are designed for use on a person in sudden cardiac arrest who is: -Unresponsive when shaken -Not breathing normally If in doubt, apply the pads. A training class in CPR/AED use is recommended for anyone who may use the HS1. If the person is an infant or child younger than eight years old or weighs less than 55 lbs (25 kg), use the special infant/child pads.
Philips is recalling HeartStart Home and OnSite (HS1) automated external defibrillators (AEDs) because one or both contact pins may be contaminated by residue from the soldering process. This contamination could prevent an adequate connection between the pads cartridge and the AED. If poor contact between the pads cartridge and AED occurs, the device may be unable to deliver therapy in an emergency.
- 2014-03-26FDA-DevicePhilips Medical Systems North America Inc.Class IIPhilips HeartStart FR3 Automated External Defibrillator (AED), models 861388 and 861389. The HeartStart FR3 is a battery powered automated external defibrillator (AED) designed for use by responders who have been trained in Basic Life Support (BLS), Advanced Life Support (ALS), or another physician-authorized emergency medical response program. The HeartStart FR3 is used to treat suspected victims of ventricular fibrillation (VF), the most common cause of sudden cardiac arrest (SCA), and cert
Philip's is recalling HeartStart FR3 Automated External Defibrillator (AED) because the Printed Circuit Board (PCB), which contains the circuitry that supplies energy to the device, could become separated from the electrical contact points that hold the board in place. In the event the PCB becomes separated from the electrical contact points, the AED may not be ready to deliver a shock in the event of an emergency.
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