Complete FDA and NHTSA recall records dated in December 2017.
These records include useful source details for the selected month.
Products were made with a seasoning component that contains a milk ingredient that has the potential to be contaminated with Salmonella.
The recall is being initiated due to mold contamination and "popped lids".
The products may contain an undeclared milk allergen.
ALDI has voluntarily recalled Choceur Dark Chocolate Bars due to the potential presence of almond pieces, which are an undeclared treenut allergen.
The products may contain an undeclared milk allergen.
Products were made with a seasoning component that contains a milk ingredient that has the potential to be contaminated with Salmonella.
Firm was notified by customer that the back panel (ingredients and nutrition facts) was incorrect on three snack mixes. Principal display label is correct which shows the main ingredients…
Plastic material was found in unbaked Meyer Lemon Cookies at retail store.
Creative Contract Packaging LLC is voluntarily recalling two code dates of HERB-OX Beef Flavor Granulated Bouillon, due to the potential presence of an undeclared milk allergen.
Products were made with a seasoning component that contains a milk ingredient that has the potential to be contaminated with Salmonella.
The products may contain an undeclared milk allergen.
The products may contain an undeclared milk allergen.
The products may contain an undeclared milk allergen.
The products may contain an undeclared milk allergen.
Products were made with a seasoning component that contains a milk ingredient that has the potential to be contaminated with Salmonella.
Products were made with a seasoning component that contains a milk ingredient that has the potential to be contaminated with Salmonella.
Firm was notified by customer that the back panel (ingredients and nutrition facts) was incorrect on three snack mixes. Principal display label is correct which shows the main ingredients…
The recall is being initiated due to mold contamination and "popped lids".
Marketed Without An Approved NDA/ANDA: FDA analysis found the product to contain undeclared sildenafil and tadalafil and undeclared milk. The presence of sildenafil and tadalafil makes AMPT…
Subpotent Drug: found to be below the specification for labeled assay.
Labeling: Incorrect Instructions. "TABLETS IN WEEK 4 ARE INACTIVE" printed on the blister foil and package insert, however,all tablets are active.
Stability Data Does Not Support Expiry: lots do not have stability that supports the use of the container system.
Subpotent Drug: found to be below the specification for labeled assay.
Stability Data Does Not Support Expiry: lots do not have stability that supports the use of the container system.
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.
