Complete FDA and NHTSA recall records dated in 2017, 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.
Bakery products which contain an ingredient which contain egg do not declare egg on the label
Foreign animal matter was allegedly found in a single container of the salad.
Potential Listeria monocytogenes contamination.
Bakery products which contain an ingredient which contain egg do not declare egg on the label
TP Food Processing, Inc. is recalling Lemongrass Satay and Shrimp Satay because the acidified sauces were not properly produced making them susceptible to contamination with Clostridium…
The firm was notified that the product may contain Listeria monocytogenes.
Potential Listeria monocytogenes contamination.
Potential Salmonella contamination of spice packet within chili kits.
Bakery products which contain an ingredient which contain egg do not declare egg on the label
A raw material initially failed testing Staphylococcus aureus. A retest was conducted with passing results but an out of specification investigation was not properly conducted leaving…
Bakery products which contain an ingredient which contain egg do not declare egg on the label
Potential Listeria monocytogenes contamination.
Bakery products which contain an ingredient which contain egg do not declare egg on the label
Bakery products which contain an ingredient which contain egg do not declare egg on the label
Potential Listeria monocytogenes contamination.
Potential Listeria monocytogenes contamination.
The firm was notified that the product may contain Listeria monocytogenes.
Potential Listeria monocytogenes contamination.
Bakery products which contain an ingredient which contain egg do not declare egg on the label
Bakery products which contain an ingredient which contain egg do not declare egg on the label
Product in principal display panel identified as Octopus and real content is squid.
A raw material initially failed testing Staphylococcus aureus. A retest was conducted with passing results but an out of specification investigation was not properly conducted leaving…
Marketed without an Approved NDA/ANDA; FDA analysis has found the product to be tainted with human chorionic gonadotropin, rendering it an unapproved drug
Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile.
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.
