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.
- 2023-12-01USDAClass IDon't eat Pelleh Poultry ready-to-eat meat products
Product Contamination
- 2023-11-30CPSCShree Ashtavinayak LLC, dba Klickpick Home, of Throop, PennsylvaniaKlickpick Home Recalls Stainless Steel Children's Cup Sets Due to Violation of Federal Lead Content Ban; Sold Exclusively at Amazon.com (Recall Alert)
The bottom exterior of the stainless-steel cups contains an accessible solder bead with levels of lead that exceed the federal lead content ban. Lead is toxic if ingested by young children and can cause adverse health effects. In addition, the lid can crack and break during use producing sharp edges and small parts, posing laceration and choking hazards to children.
- 2023-11-30CPSCFENGM (Hong Kong Fengmang International Co. Ltd.), of ChinaTiblue Stainless Steel Children's Cups Recalled Due to Violation of Federal Lead Content Ban; Sold Exclusively on Amazon.com by FENGM (Recall Alert)
The bottom exterior of the stainless-steel cups contains an accessible solder bead with levels of lead that exceed the federal lead content ban. Lead is toxic if ingested by young children and can cause adverse health effects. In addition, the lid can crack and break during use producing sharp edges and small parts, posing laceration and choking hazards to children.
- 2023-11-30CPSCDODO Baby House, of ChinaPack and Play Mattresses Recalled Due to Suffocation Hazard for Infants; Violations to the Federal Safety Regulation for Crib Mattresses; Sold Exclusively on Amazon.com by DODO Baby House (Recall Alert)
The recalled mattresses violate multiple provisions of the federal safety regulation for crib mattresses, including the thickness test and missing warnings and labels. The product poses a suffocation hazard to infants.
- 2023-11-30CPSCBeyond Baby, of ChinaVibe Bear Playyard Mattresses Recalled Due to Suffocation Hazards for Infants; Violation of the Federal Safety Regulation for Crib Mattresses; Sold Exclusively on Amazon.com by Beyond Baby (Recall Alert)
The recalled mattresses violate multiple provisions of the Safety Standard for Crib Mattresses, including the firmness and thickness tests and missing warnings and labels. The product poses a suffocation hazard to infants.
- 2023-11-30CPSCPeg Perego SPA, of ItalyPeg Perego Recalls Inclined Sleeper Bassinets for YPSI and Z4 Strollers Due to Risk of Suffocation and Fall Hazard; Violation of Federal Safety Standards (Recall Alert)
The recalled bassinets violate the Safe Sleep for Babies Act because they were marketed for infant sleep and have an incline angle greater than 10 degrees. Infant fatalities have occurred in inclined sleeper products after the infants rolled from their back to their stomach or side while unrestrained, or under other circumstances. The bassinets also violate the Infant Sleep Products regulation because they do not have a stand.
- 2023-11-29FDA-DeviceSunMed Holdings, LLCClass IIMedline manual resuscitators with integrated manometer, multiple accessory configurations to include: 1. Adult Resuscitator REF #s: CPRM1116FPM, CPRM1116FPM4, CPRM1116M, CPRM1116MC, CPRM1116PM, CPRM1116PMT, CPRM1126FM, CPRM1126FPM, CPRM1126FPWM, CPRM1126M; 2. Infant Resuscitator REF #s: CPRM3312FM, CPRM3312FM123, CPRM3312FPM, CPRM3312FPM3, CPRM3312FPMC, CPRM3312M, CPRM3312M3, CPRM3312P3M3, CPRM3312PM, CPRM3312PM2, CPRM3312PMC2, CPRM3312PMTD1, CPRM3312PMX, CPRM3312PWM, CPRM3322FM, CPRM332
A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing.
- 2023-11-29FDA-DeviceSunMed Holdings, LLCClass IICuraplex manual resuscitators with integrated manometer, multiple accessory configurations to include: 1. Curaplex Adult Premium BVM with Bag Reservoir, Manometer, Filter, Peep Valve & Mask, REF # 2442-BVMPAD; 2. Curaplex Child Premium BVM with Bag Reservoir, Manometer, 25cm Pop-off, Filter & Mask, REF # 2442-BVMPCH; 3. Curaplex Child Premium BVM with Bag Reservoir, Manometer, 25cm Pop-off, Filter, Infant and Neonate Mask, REF # 2442-BVMCIN; 4. Curaplex Infant Premium BVM with Ba
A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing.
- 2023-11-29FDA-DeviceSunMed Holdings, LLCClass IIVentlab, LLC V-Care manual resuscitators with integrated manometer, multiple accessory configurations to include: 1. V-Care Child Resuscitator REF #s: VN4100MB, VN4100MCFB-3, VN4100MCP; 2. V-Care Infant Resuscitator REF #s: VN3100OB, VN3100MB-2, VN3100MB-M01, VNW3100MB-2, VN3100MBP-3M, VN3100MB, VN3100MB-D1, VN3100MB-M00-0, VN3100MB-M1, VN3100OBP, VN3100MB-B, VN3100MB-I, VN3100MBP-000, VN3100MBP-2, VN3100MB-PW2, VN3100MBP, VN3100MBP-D1, VN3100MBPW-D2, VN3100MBP-F, VN3100MXK-2, VN3100MX-F,
A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing.
- 2023-11-29FDA-DeviceSunMed Holdings, LLCClass IIVentlab, LLC STAT-Check manual resuscitators with integrated manometer, multiple accessory configurations to include: 1. STAT-Check Adult Resuscitator REF #: SC9101B; 2. STAT-Check Infant Resuscitator RES #s: SC7101B & SC7101B-M0; 3. STAT-Check Pediatric Resuscitator REF #: SC8121B.
A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing.
- 2023-11-29FDA-DeviceSunMed Holdings, LLCClass IIVentlab, LLC SafeSpot manual resuscitators with integrated manometer, multiple accessory configurations to include: 1. SafeSpot Infant Resuscitator REF #s: SS3200OBPC-T, SS3204MB-D12, SS3200MB-2, SS3200MB-D1, SS3200OBP, SS3200MB-MMC, SS3200MBP-M00, SS3200MB-PW, SS3200MBP-2I, SS3200MBF-2, SS3204MBF-2, SS3200MB- PWS10, SS3206MCP-S1, SS3204MB, SS3204MC-P2, SS3200MB, SS3200MBP-2, SS3200MBF, SS3200MB-I, SS3200MBP, SS3200OB, SS3200MC, SS3200MC-P2; 2. SafeSpot Safe Spot Bag, D1 Mask with Inflatio
A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing.
- 2023-11-29FDA-DeviceSunMed Holdings, LLCClass IIVentlab, LLC RescuMed manual resuscitators with integrated manometer, multiple accessory configurations to include: 1. RescuMed Adult Resuscitator REF #s: BVM510-F, BVMB510-10, BVMB510-F, BVMB510S-F; 2. RescuMed Infant Resuscitator REF #s: BVMB710 & BVMB710-F; 3. RescuMed Pediatric Resuscitator REF #s: BVMB812, BVMB812-F, BVMB810, BVMB810-F, BVMB810S-F.
A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing.
- 2023-11-29FDA-DeviceSunMed Holdings, LLCClass IIVentlab, LLC Horizon manual resuscitators with integrated manometer, multiple accessory configurations to include: 1. Horizon Adult Resuscitator REF #s: 9122HZ, HZI9000, HZI9108, 9106HZ, 9110HZ, 9120HZ, 9111HZ, 9100HZ, 9105HZ, 9108HZ, 9006HZ, 9002HZ; 2. Horizon Infant Resuscitator REF #s: 6112HZ, 6123HZ, 6125HZ, 6200HZ, 6106HZ, 6118HZ, 6107HZ, 6013HZ, 6117HZ, 6116HZ, 6019HZ, HZI6000, 6009HZ; 3. Horizon Pediatric Resuscitator REF #s: 8106HZ, 8119HZ, 8115HZ, 8107HZ, 8010HZ, 8004HZ, 8105H
A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing.
- 2023-11-29FDA-DeviceSunMed Holdings, LLCClass IIVentlab, LLC BreathTech manual resuscitators with integrated manometer, multiple accessory configurations to include: 1. BreathTech Adult Resuscitator REF #s: BT5107F & BT5104P; 2. BreathTech Child Resuscitator REF #s: BT3030, BT3034, & BT3025; 3. BreathTech Infant Resuscitator REF #s: BT2415K, BT2416, BT2032, BT2016, BT2035, BT2216, BT2036, BT2023, BT2026, BT2220-2, BT2020, BT2220, BT2220F, BT2215, BT2415, BT2014, BT2027, BT2015, BT2029, BT2037, BT2048, BT2034, BT2034W, BT2234, BT223
A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing.
- 2023-11-29FDA-DeviceSunMed Holdings, LLCClass IIVentlab, LLC AirFlow manual resuscitator devices with integrated manometer, multiple accessory configurations to include: 1. AirFlow Adult Resuscitator REF #s: AF1140MB-M5, AF1140MB-D5, AF5142OB, AF5142MB, AF5142MB-D235, AF1142MBP, AF5142MBP, AF5140MB, AF5140MB-2, AF5140MB-D6, AF5140MB-F, AF1140MB-T, AF1140MB-PW, AF5140MB-PW, AF1140MB-I, AF5140MB-I, AF5140MBN, AF1140MBS, AF5140MBS, AF1140MB-X, AF5140MB-X, AF1140MB-P, AF5140MBP, AF1140MB-K, AF5140MBS-I,AF5140MBPF-G10, AF5140MBP-G10, AF1140MBP
A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing.
- 2023-11-29FDA-DeviceAizu Olympus Co., Ltd.Class IIUretero-reno fiberscope-For endoscopic diagnosis and treatment within the ureter and kidney. Model Numbers: URF-P7, URF-P7R, URF-V2, URF-V2R, URF-V3, URF-V3R.
Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection
- 2023-11-29FDA-DeviceAizu Olympus Co., Ltd.Class IIUreteralscope- for endoscopic diagnosis and treatment within the ureter, kidney and biliary tract (common bile duct and hepatic duct). Model Numbers: URF-P6, URF-P6R.
Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection
- 2023-11-29FDA-DeviceAizu Olympus Co., Ltd.Class IICystonephroscope-endoscopic diagnosis and treatment within the bladder, urethra, and kidney Model Numbers: CYF-5, CYF-VH, CYF-VHR.
Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection
- 2023-11-22FDA-DevicePhilips North AmericaClass IISpectral CT on Rails, Software Version 5.1.0, Model Number 728334
This recall is part of a 2-issue recall for the same system. When using the IVC needle position button, on the IVC control box during a series of scans, the plan box may not move to the desired needle position. This issue could result in the gantry moving to a location the operator does not expect. If this occurs, it presents a risk that the scan could occur at an incorrect location, or that the unintended motion of the gantry could cause a collision with the user or needle. The other part of the recall involves a software crash when the CCT foot pedal is activated (as described in RES ID93363).
- 2023-11-22CPSCPandaEar, of Lake Dallas, TexasPandaEar Recalls Stainless Steel Children's Cups Due to Violation of Federal Lead Content Ban; Sold Exclusively on Amazon.com (Recall Alert)
The bottom exterior of the recalled stainless-steel cups contains an accessible solder bead with levels of lead that exceed the federal lead content ban. Lead is toxic if ingested by young children and can cause adverse health effects. In addition, the lid can crack and break during use producing sharp edges and small parts, posing choking and laceration hazards to children.
- 2023-11-19USDAClass IDo not use Skyline Provisions ground beef
Product Contamination
- 2023-11-16CPSCTarget Corporation, of Minneapolis, MinnesotaTarget Recalls Hearth & Hand™ with Magnolia Toy Mushroom Peg Sorters Due to Choking Hazard (Recall Alert)
The stems of the toy mushrooms can detach, posing a choking hazard to young children.
- 2023-11-16CPSCLAOION, of ChinaStainless Steel Children's Cups Recalled Due to Violation of Federal Lead Content Ban; Sold Exclusively at Amazon.com by LAOION (Recall Alert)
The bottom exterior of the stainless-steel cups contains an accessible solder bead with levels of lead that exceed the federal lead content ban. Lead is toxic if ingested by young children and can cause adverse health effects. In addition, the lid can crack and break during use producing sharp edges and small parts, posing choking and laceration hazards to children.
- 2023-11-16CPSCTractor Supply Company, of Brentwood, TennesseeTractor Supply Company Recalls Red Shed Hammock Swing Chairs Due to Fall Hazard
A plastic buckle that supports the back of the chair can break when a consumer is seated in the chair, posing a fall hazard.
- 2023-11-15FDA-FoodAbbott LaboratoriesClass IISimilac Probiotic Tri-Blend - 0.017oz (0.50g) packaged in foil packets. 50 foil packets per carton - 3 cartons per case.
Marketed towards preterm infants without approval as a new drug or licensed biologic, as well as unsafe food additive
- 2023-11-15FDA-DrugGrato Holdings, Inc.Class IIIV-FORCE Homeopathic, 1 FL OZ (30 ml) per glass bottle, Distributed by: BioActive Nutritional, Inc., 1803 N. Wickham Rd., Melbourne, FL 32935
Incorrect Product Formulation: product contains Active Ingredient Glandula Suprarenalis Suis 8X instead of Glandula Suprarenalis Bovine 8X (as stated on the product label).
- 2023-11-09CPSCiMOONZZZ, of ChinaChildren's Nightgowns Recalled Due to Burn Hazard and Violation of Federal Flammability Standards; Sold by iMOONZZZ Exclusively on Amazon.com
The children's nightgowns fail to meet the flammability standards for children's sleepwear, posing a risk of burn injuries to children.
- 2023-11-08FDA-DrugPadagis US LLCClass IIGynazole-1, (Butoconazole Nitrate) Vaginal Cream USP, 2%, Net Wt 5.8 g per pre-filled applicator, packaged in 1 prefilled applicator per carton, Rx Only, Manufactured By Padagis, Yeruham, Israel; Distributed By: Padagis, Allegan, MI 49010. NDC: 45802-396-01
Incorrect Product Formulation: Hydrophilic Colloidal Silica was used to manufacture the product rather than Hydrophobic Colloidal Silica as required by the manufacturing process.
- 2023-11-06NHTSA-EquipmentEvenflo Company, Inc.Evenflo Company, Inc. — Missing Warning Labels/FMVSS 213
A child seat missing warning labels will not inform the owner of critical safety information, which can increase the risk of injury for the child seat occupant.
- 2023-11-02CPSCUncleWu Life LLC, of Avondale, ArizonaUncleWu Life Recalls Infant Bath Seats Due to Drowning Hazard; Violation of Bath Seat Requirements; Sold Exclusively on Amazon.com (Recall Alert)
The bath seats fail to meet the federal safety regulation for infant bath seats, including requirements for stability and leg openings, and can tip over while in use, posing a drowning hazard to babies.
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