Deutsch Kase Haus Semi Soft cheese with yogurt cultures and with or without recall — FDA F-1896-2017
Potential Listeria monocytogenes contamination.
Complete FDA and NHTSA recall records dated in May 2017.
These records include useful source details for the selected month.
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.
Supotent: Out of Specification result for assay test during routine stability testing.
Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile.
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.