92,900 total recalls in our database
Unknown Manufacturer
The recalled crib bumpers violate the federal crib bumper ban, posing a deadly suffocation hazard to infants. Padded crib bumpers are banned by the federal Safe Sleep for Babies Act.
Unknown Manufacturer
The stroller fan's housing allows consumers' fingers to contact the fan's blade, posing a laceration injury hazard to small children.
Unknown Manufacturer
The recalled unassembled Deluxe Pit Kit slot cars violate the mandatory federal regulation for magnets because the magnets used to power the car are loose prior to assembly, posing an ingestion hazard to children. Assembled models do not pose this risk and are therefore not subject to this recall. When high-powered magnets are swallowed, the ingested magnets can attract each other, or another metal object, and become lodged in the digestive system. This can result in perforations, twisting and/or blockage of the intestines, infection, blood poisoning and death.
Taylor Water Technologies LLC, of Sparks, Maryland
The recalled Taylor Water Technologies reagent bottles sold with test kits contain sulfuric acid, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act (PPPA). The packaging for the bottle with sulfuric acid is not child resistant, posing a risk of chemical burns to the skin or eyes and internal corrosive burns, if ingested.
Rajbhog Distributors TX
Undeclared milk
Product may contain egg, an undeclared allergen.
Rajbhog Distributors TX
Undeclared milk
Undeclared Yellow #5
Rajbhog Distributors TX
Undeclared milk
Nestle-USA, Inc. (Corporate Office)
Firm received complaints of infant choking.
Potato flour item #20501 was recalled due to undeclared milk (between 13ppm and 17ppm).
FRESHPOINT CENTRAL FLORIDA
Mislabeled salads (undeclared peanut allergen). Incorrect ingredient applied (peanuts)
Nestle-USA, Inc. (Corporate Office)
Firm received complaints of infant choking.
Undeclared Yellow #5
Product may be contaminated with foreign objects (white fragments of plastic, varying in length and width).
Small pieces of plastic broken tray in the product.
Defective Container: Some packets may not be fully sealed, potentially allowing for loss of Ethanol from the product.
Lack of Assurance of Sterility: due to a quality control process deviation. During an internal quality assurance review, an Acceptable Quality Limit (AQL) inspection was not conducted on a statistically sound number of samples. This may result in the inability to assure that the impacted products meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess and may lead to products of unacceptable quality.
Wuxi Medical lnstrument Factory Co.
Lack of assurance of sterility and cGMP deviations observed at the manufacturing site.
Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices