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.
Mitragyna Speciosa Leaf Powder Thai Maeng Da Kratom product is being recalled because they have the potential to be contaminated with Salmonella
Ignite High Endurance Pre-Workout Supplement with Caffeine dietary supplement product is recalled because label declared WHEY protein but do not declare milk.
Wysong Corporation is conducting a voluntary recall of multiple varieties of Protein Key brand protein meals due to undeclared allergen soy.
Shipping container from CA to HI was not held at proper temperature which could cause food items to be contaminated with spoilage organisms or pathogens
Cinnamon Sugar Cookie is recalled because the ingredient statement declared milk but the Contains statement declared only Dairy.
Wysong Corporation is conducting a voluntary recall of multiple varieties of Protein Key brand protein meals due to undeclared allergen soy.
Wysong Corporation is conducting a voluntary recall of multiple varieties of Protein Key brand protein meals due to undeclared allergen soy.
Wysong Corporation is conducting a voluntary recall of multiple varieties of Protein Key brand protein meals due to undeclared allergen soy.
Mitragyna Speciosa Leaf Powder Green Horn Kratom product is being recalled because they have the potential to be contaminated with Salmonella
Shipping container from CA to HI was not held at proper temperature which could cause food items to be contaminated with spoilage organisms or pathogens
Shipping container from CA to HI was not held at proper temperature which could cause food items to be contaminated with spoilage organisms or pathogens
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Failed Dissolution Specification: Low dissolution outside of specifications
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
There is an increased risk of false positive Proteus results when the product is used with specific types of BD BACTEC blood culture bottles.
Inaccurrate flow readings. Depending on the degree of inaccuracy, this issue may not be easy for the user to detect during setup or use (for example, following a Flow Probe relocation or…
A component of the kit was found to contain bacterial contamination.
Products do not meet the labeled sterility claim of a Sterility Assurance Level (SAL) 10-6.
The secondary packaging is labeled with an incorrect expiration date.
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.
