United States Recalls
Consumer recalls from the FDA, CPSC, NHTSA, and USDA FSIS.
Joolz Recalls Aer2 Car Seat Adapters for Strollers Due to Risk of Serious Injury...
The baby loungers violate the mandatory standard for Infant Sleep Products because the sides are shorter than the minimum side height limit to secure the infant; the sleeping pad's thickness exceeds the maximum limit, posing a suffocation hazard; and an infant could fall out of an enclosed opening at the foot of the lounger or become entrapped. The portable loungers do not have a stand, posing a fall hazard. These violations create an unsafe sleeping environment for infants, posing a risk of serious injury or death.
SHEIN Distribution Corporation Recalls Michley Children's Pajamas Due to Risk of...
The recalled children’s pajamas violate the mandatory flammability standard for children’s sleepwear, posing a risk of serious burn injuries or death.
Spa Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment...
The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and drowning hazards to consumers.
Veseacky Pajama Sets Recalled Due to Risk of Serious Injury Death from Burn Haza...
The pajama sets violate the mandatory safety standards for children's sleepwear, posing a risk of serious injury or death to children from burns.
Piaggio Group Americas, Inc. - Headlight May Fail
Loss of lighting can reduce visibility, increasing the risk of a crash.
Joolz Recalls Aer2 Car Seat Adapters for Strollers Due to Risk of Serious Injury...
The recalled car seat adapters can fail to properly attach to the stroller, which may allow the car seat to fall, posing a risk of serious injury from a fall hazard.
Power Plate Meals, LLC Recalls Frozen Meatloaf Products Due to Misbranding and U...
Unreported Allergens
General Motors, LLC - Third-Row Power Folding Seatback May Trap Occupant
A person, especially a child, may be trapped by a rear powered seatback, increasing their risk of injury.
Mahurkar Elite PASS Trays; Description (Product Number/CFN): 12 FR x 13cm Acut...
The Tegaderm CHG dressing, as specified in product labeling, was missing from certain lots of Mahurkar Elite PASS Trays.
WeiKFiELD Custard Powder Kesar Pista, Net Wt. 300g (10.6 OZ.), Poly Jar , 24 uni...
The ingredient, Pista, currently declared on our label should be corrected to the standard American nomenclature, Pistachio.
CGuard Prime Carotid Stent System, 135cm, 9mx30mm Model/Catalog Number: CND093...
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
DOXOrubin Hydrochloride Liposome injection, 50 mg/25 mL (2mg/mL), 25 mL single-d...
Presence of Particulate matter: Particulate matter identified as glass.
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUL...
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
MOSAIQ Oncology Information System
Software may fail to load adapted baseline shift plan during treatment delivery when a communication error occurs.
Minocycline Hydrochloride Extended-Release Tablets, USP, 115 mg, 30-count bottle...
Failed Dissolution Specifications: An out-of-specification (OOS) result was observed during the 9th month of dissolution test analysis
Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Product Name: SPO...
Due to incorrect incubation process being performed on product.
Marquesita de Dulceleche [image] Delighted Flavored Cakes The Original, Net Wt. ...
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number...
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Duloxetine Delayed-Release Capsules, USP, 60mg, packaged in a) 90 Capsules (NDC ...
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
Allia Moveo angiographic X-ray system
GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.
Orca Single Use Air/Water and Suction Valves, Material Number (UPN) SUV-617-50; ...
Boston Scientific is initiating a medical device removal of Orca Sterile, Single Use Air/Water and Suction Valves due to a higher than anticipated occurrence of the suction button sticking.
Cake de Mango [image] Mango Cake The Original, Net Wt. 47 oz, packaged in a rigi...
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUS...
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
NEURO NOURISH dietary supplement; 6-IN-1 PREBIOTIC, PROBIOTIC, VITAMIN, MINERAL,...
Premature lipid oxidation causing quality issue potentially causing product to have an off odor and bitter taste.