Complete FDA and NHTSA recall records dated in 2018, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
Stryker Neurovascular has become aware that at least 1 (one) Trevo XP Provue System was manufactured where the carton sleeve did not match the physical contents of the pack.
Philips has identified that certain fasteners cannot be confirmed to have been torqued according to specification. If the fasteners were not torqued as specified and a failure occurs while…
Product labeling for TRYPTIK 2-C-PLATE Self Tapping screw, REF TRY-PS 40, Lot 3-5934 contains the sketch/drawing of a self-drilling screw.
Product labeling for TRYPTIK 2-C-PLATE Self Tapping screw, REF TRY-PS 40, Lot 3-5934 contains the sketch/drawing of a self-drilling screw.
Boston Scientific has received reports of intermittent over-sensing of the Minute Ventilation (MV) sensor signal with certain Boston Scientific pacemaker and cardiac resynchronization…
The product has been recalled because it has the potential to be contaminated with a chemical pesticide residue.
Customer tested product and found Listeria monocytogenes in frozen tuna fillet saku
An intermittent ingredient statement labeling error by the firm's label printing company led to the firm's Pecan Divinity products being mislabeled with the ingredients for its Coconut Bon…
A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
Product may be contaminated with Listeria monocytogenes.
State of Massachusetts tested product and found it to be positive for Salmonella
Undeclared soy. Firm was notified by a consumer that they found chicken in the product. The chicken contains soy.
Gel Spice, Inc. is recalling three beef flavored bouillon cube products because they contain undeclared allergens -- soy and wheat.
A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
Product may be contaminated with Listeria monocytogenes.
An intermittent ingredient statement labeling error by the firm's label printing company led to the firm's Pecan Divinity products being mislabeled with the ingredients for its Coconut Bon…
A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
REEF NET brand Wild Pacific Smoked Salmon, Ready-To-Eat product, is recalled due to undeclared soy lecithin. The firm used soy release agent but did not declare soy lecithin in the…
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.
