Touchat Large Fuzzy Area Rugs
Unknown Manufacturer
The recalled area rugs violate the mandatory federal flammability regulations for carpets and rugs, posing a fire hazard.
95,018 total recalls in our database
Unknown Manufacturer
The recalled area rugs violate the mandatory federal flammability regulations for carpets and rugs, posing a fire hazard.
Unknown Manufacturer
The speaker's lithium-ion battery can overheat and catch fire, posing burn and fire hazards to consumers.
Unknown Manufacturer
The zipline's stainless-steel cable can break, posing a fall hazard.
THE COCA-COLA COMPANY
The potential presence of a foreign metal object in the product, i.e. a stainless-steel ring.
Samsung Bean Sprout
Listeria monocytogenes.
THE COCA-COLA COMPANY
The potential presence of a foreign metal object in the product, i.e. a stainless-steel ring.
Consumer complaints involving floating particles.
Product contains Acid Red 18
Kick Ash Products
Undeclared allergen (almond) in Dark Chocolate Cherry Granola
AJI MORI SAUCE
Potential contamination with Clostridium botulinum
Product contains Acid Red 18
THE COCA-COLA COMPANY
The potential presence of a foreign metal object in the product, i.e. a stainless-steel ring.
HP Hood (VERNON)
Undeclared pineapple, sugar, modified corn starch, natural flavors, phosphoric acid
IntegraDose Compounding Services
Lack of Assurance of Sterility: leaking bags
Lack of Assurance of Sterility: Firm did not perform process validation.
Labeling: Incorrect or missing Package Insert: There is an error on the Package Insert (PI), section 2.3, Preparation, Handling, and Administration. The concentration of the reconstituted product is listed as '20 mg per vial.' This information should read: '20 mg per mL'.
B. Braun Medical
Lack of assurance of sterility: bags have the potential to leak..
Glenmark Pharmaceuticals Inc., USA
Failed Dissolution Specifications: Out of Specification (OOS) was reported in test of dissolution at the 12th month time point in long term stability study.
Lack of Assurance of Sterility: Firm did not perform process validation.
Labeling: Incorrect or missing Package Insert: There is an error on the Package Insert (PI), section 2.3, Preparation, Handling, and Administration. The concentration of the reconstituted product is listed as '20 mg per vial.' This information should read: '20 mg per mL'.