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.
- 2018-01-25CPSCVTech Electronics Limited, of ChinaVTech Recalls Infant Rattles Due to Choking Hazard
The ears on the elephant rattles can break off, posing a choking hazard to young children.
- 2018-01-19CPSCPanasonic Corporation of North America, of Newark, N.J.Panasonic Recalls Flat Screen Televisions and Swivel Stands Due to Tip-Over Hazard
The mounting screws that connect the swivel stand to the television can come loose and cause the television to tip over and fall off the stand unexpectedly, posing serious tip-over and entrapment hazards that can result in injuries or death to children.
- 2018-01-18CPSCMultipro Limited, of IndiaBassinets Recalled Due to Violation of Bassinet & Cradle Standard; Made By Multipro (Recall Alert)
The bassinets fail to meet the mandatory federal safety standard for bassinets and cradles, posing fall and entrapment hazards to babies.
- 2018-01-17FDA-DrugDr. Reddy's Laboratories, Inc.Class IIDocetaxel Injection USP, 20 mg/mL, One-Vial Formulation, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Visakhapatnam - 530 046 INDIA, NDC 43598-611-11
Defective Container: Product complaints received of defect in the seal of the Docetaxel injection vials that the aluminum seal and/or stopper is removed when the cap is flipped off.
- 2018-01-09CPSCSkip Hop, Inc., of New YorkSkip Hop Recalls Convertible High Chairs Due to Fall Hazard
The front legs on the highchair can detach from the seat, posing fall and injury hazards to children.
- 2018-01-03FDA-DeviceAccuray IncorporatedClass IITomoHDA(R) System, Model Number 1018286 Product Usage: The TomoTherapy treatment system is intended to be used as an integrated system for t he planning and precise delivery of radiation therapy, stereotactic radiotherapy, or stereotactic radiosurgery to tumors or other targeted tissues while minimizing the delivery of radiation to vital healthy tissues. The megavoltage x-ray radiation is delivered in a rotational, non-rotational, modulated (IMRT), or non- modulated (non-IMRT/3 dimensional c
Uncontrolled couch Z-axis movement (descent)
- 2018-01-03FDA-DeviceAccuray IncorporatedClass IITomoH(R) System, Model Number 1018284 Product Usage: The TomoTherapy treatment system is intended to be used as an integrated system for t he planning and precise delivery of radiation therapy, stereotactic radiotherapy, or stereotactic radiosurgery to tumors or other targeted tissues while minimizing the delivery of radiation to vital healthy tissues. The megavoltage x-ray radiation is delivered in a rotational, non-rotational, modulated (IMRT), or non- modulated (non-IMRT/3 dimensional con
Uncontrolled couch Z-axis movement (descent)
- 2018-01-03FDA-DeviceAccuray IncorporatedClass IITomoHD(R) System, Model Number 1018283 Product Usage: The TomoTherapy treatment system is intended to be used as an integrated system for t he planning and precise delivery of radiation therapy, stereotactic radiotherapy, or stereotactic radiosurgery to tumors or other targeted tissues while minimizing the delivery of radiation to vital healthy tissues. The megavoltage x-ray radiation is delivered in a rotational, non-rotational, modulated (IMRT), or non- modulated (non-IMRT/3 dimensional co
Uncontrolled couch Z-axis movement (descent)
- 2018-01-03FDA-DeviceAccuray IncorporatedClass IIHi-Art(R) System, Model Number H-000-0003 Product Usage: The TomoTherapy treatment system is intended to be used as an integrated system for t he planning and precise delivery of radiation therapy, stereotactic radiotherapy, or stereotactic radiosurgery to tumors or other targeted tissues while minimizing the delivery of radiation to vital healthy tissues. The megavoltage x-ray radiation is delivered in a rotational, non-rotational, modulated (IMRT), or non- modulated (non-IMRT/3 dimensional
Uncontrolled couch Z-axis movement (descent)
- 2018-01-02CPSCComfort Research LLC, of Grand Rapids, Mich.Comfort Research Recalls Bean Bag Chair Covers Due to Risks of Entrapment, Suffocation to Children
The zippers on the bean bag chair covers can be opened by children who can then crawl inside, become entrapped, suffocate or choke on the bean bag chair's foam beads.
- 2017-12-28CPSCLand of Nod, of Morton Grove, Ill.The Land of Nod Recalls Toddler Beds Due to Entrapment Hazard (Recall Alert)
The headboard can disconnect from the bed frame and fall onto the bed, posing an entrapment hazard to children.
- 2017-12-21CPSCWohali Outdoors LLC, of Broken Arrow, Okla.Wohali Outdoors Recalls Children's Sleepwear Due to Violation of Federal Flammability Standard; Sold Exclusively at Bass Pro Shops
The children's pajama sets fail to meet flammability standards for children's sleepwear, posing a risk of burn injuries to children.
- 2017-12-21NHTSA-EquipmentChrysler (FCA US, LLC)Chrysler (FCA US, LLC) — Fire Extinguisher May Be Clogged or Inoperable
If the fire extinguisher does not function properly, it can increase the risk of injury in the event of a fire.
- 2017-12-20FDA-DevicePhysio-Control, Inc.Class ILIFEPAK(R) Electrode Starter Kits, Catalog # 11101-000017, MIN #3202784-009 The defibrillation electrodes are used only with LIFEPAK EXPRESS(R) AED, LIFEPAK CR(R) Plus AED, LIFEPAK 1000 defibrillator, or LIFEPAK 500 Biphasic AED s with a pink connector.
The infant artwork on the product instructs incorrect pad placement. Also, the artwork is missing the Type BF Patient connection and High Voltage Warning symbols.
- 2017-12-20FDA-DevicePhysio-Control, Inc.Class ILIFEPAK(R) defibrillation electrodes, Catalog # 11101-000016, MIN #3202380-006 The defibrillation electrodes are used only with LIFEPAK EXPRESS(R) AED, LIFEPAK CR(R) Plus AED, LIFEPAK 1000 defibrillator, or LIFEPAK 500 Biphasic AED s with a pink connector.
The infant artwork on the product instructs incorrect pad placement. Also, the artwork is missing the Type BF Patient connection and High Voltage Warning symbols.
- 2017-12-19CPSCManu Changzhou Future International Business Mafacturer, from ChinaSquatty Potty Recalls Children's Toilet Step Stools Due to Injury and Fall Hazards
The top removable step (hat) on the recalled children's toilet step stools can detach while a child is standing on it, posing injury and fall hazards.
- 2017-12-16USDAClass IDon't eat Piller's Fine Foods salami or prosciutto
Product Contamination
- 2017-12-13FDA-DeviceICU Medical IncClass IIICU Mednet(TM) Medication Management Suite 6.1 and 6.21, Product Code/List Numbers: (a) 16037-64-01; MedNet 6.1 b) 16037-64-02; MedNet 6.1 c) 16037-64-03; MedNet 6.1 d) 16037-64-04; MedNet 6.21 The ICU Medical MedNet Medication Management Suite (MMS) is intended to facilitate networked communication between MMS compatible computer systems and MedNet compatible infusion pumps. The MMS provides trained healthcare professionals with the capability to send, receive, report, and store infor
Issue 1: The MedNet Meds 6.1 and 6.21 programs, under certain conditions, can change the piggyback medication entry set settings for existing defined medication entries. This includes (a) whether a medication may be piggybacked and (b) whether an infusion may be interrupted by a piggyback. This only occurs when: 1. Medication entries are built with the same displayed name and diluent amount AND; 2. The piggyback or interruptible settings differ from one CCA to another AND; 3. The drug library is exported then imported into the MedNet Meds program. The changed drug library may then be finalized and downloaded to infusers for use in clinical settings. The changes are made without any notice provided to either the MedNet Meds user (pharmacist) or to the clinician operating the infuser that the piggyback or interruptible settings have been altered. Issue 2: The MedNet Meds 6.1 program, under certain conditions different from those described above in Issue 1, can change the piggyback medication entry set settings for existing defined medication entries. This includes (a) whether a medication may be piggybacked and (b) whether an infusion may be interrupted by a piggyback. This only occurs when: 1. The Master Drug Formulary contains medication entries built with the same displayed name and diluent amounts but one is a Limited rule set and the other is a Full rule set AND; 2. The medication entry built as the Full rule set has a blank medication amount with the medication units in mg AND; 3. Both medication entries have different piggyback options set AND; 4. The drug library is exported then imported into the MedNet Meds program. In this case, the piggyback options will be changed during an import of such drug library.
- 2017-12-13FDA-FoodThe Kroger CoClass IIComforts FOR BABY Purified Water with Flouride Added. 1 GAL (3.78 L) DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202
the firm received a complaint of mold found in the product.
- 2017-12-12CPSCDream On Me, of Piscataway, N.J.Dream On Me Recalls Crib & Toddler Bed Mattresses Due to Violation of Federal Mattress Flammability Standard
The mattresses fail to meet the mandatory federal flammability standard for mattresses, posing a fire hazard.
- 2017-12-08CPSCKarmin Industries, of CanadaOne Stop Shop Recalls Children's Pajamas Due to Violation of Federal Flammability Standard: Sold Exclusively at Foreman Mills
The children's pajamas fail to meet the federal flammability standards for children's sleepwear, posing a risk of burn injuries to children.
- 2017-12-06FDA-DeviceZimmer Biomet, Inc.Class IIROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled electromechanical arm. It is intended to be used in the operating room for the spatial positioning and orientation of an instrument holder or tool guide. Guidance is based on a pre-operative plan developed with three-dimensional imaging software, and uses fiducial markers or optical registration. The system is intended for use by neurosurgeons to guide standard neurosurgical instruments. It is indicated for any neurosurgic
The software issue described was corrected in the modification to the MXTTOUT controller parameter settings.
- 2017-11-30CPSCNatural Solutions for Life, Inc. of Robinson, Ill.Natural Solutions for Life Recalls Synodrin Pain Relieving Cream Due to Failure to Meet Child Resistant Closure Requirement
The packaging is not child resistant as required by the Poison Prevention Packaging Act. The pain relieving cream contains lidocaine, posing a risk of poisoning to young children.
- 2017-11-29CPSCToys"R"Us Inc., of Wayne, N.J.Toys“R”Us Recalls Clay Craft Kits Due to Risk of Mold Exposure; Sold at Babies“R”Us and Toys“R”Us
Mold can be present in the clay, posing a risk of respiratory or other infections in individuals with compromised immune systems, damaged lungs or an allergy to mold.
- 2017-11-22FDA-FoodCHI GreenhouseClass IIBrightFarms Baby Romaine Mix (4 oz. package)
Bright Farms Inc. dba CHI Greenhouse LLC is initiating a voluntary recall of packaged produce due to the potential presence of E. coli.
- 2017-11-22FDA-FoodCHI GreenhouseClass IIBrightFarms Baby Arugula (4 oz. package)
Bright Farms Inc. dba CHI Greenhouse LLC is initiating a voluntary recall of packaged produce due to the potential presence of E. coli.
- 2017-11-22FDA-FoodCHI GreenhouseClass IIBrightFarms Baby Kale (3 oz. package)
Bright Farms Inc. dba CHI Greenhouse LLC is initiating a voluntary recall of packaged produce due to the potential presence of E. coli.
- 2017-11-22FDA-FoodCHI GreenhouseClass IIBrightFarms Baby Greens Blend (4 oz. and 8 oz. package)
Bright Farms Inc. dba CHI Greenhouse LLC is initiating a voluntary recall of packaged produce due to the potential presence of E. coli.
- 2017-11-22FDA-FoodCHI GreenhouseClass IIBrightFarms Baby Spinach (4 oz. and 8 oz., and 3# packages)
Bright Farms Inc. dba CHI Greenhouse LLC is initiating a voluntary recall of packaged produce due to the potential presence of E. coli.
- 2017-11-21CPSCJojo Group LLC, of Rocky River, OhioWoolino Recalls Children's Pajamas Due to Violation of Federal Flammability Standard
The children's pajama sets fail to meet flammability standards for children's sleepwear, posing a risk of burn injuries to children.
Get notified about new baby recalls
Free weekly digest. We email when a new federal recall in this category — or anything else affecting your household — is published.
Get the Sunday Brief