All Recalls

The wire size of the recalled extension cords cannot handle the appropriate amp load and lacks protective features, posing a fire hazard.

Undeclared soy (whole edamame beans)

Possible Salmonella contamination in cinnamon

Routine NY Agriculture and Markets inspection found pasteurization temperature was not recorded for two lots of cheese due to pasteurizer recorder chart malfunction.

Routine NY Agriculture and Markets inspection found pasteurization temperature was not recorded for two lots of cheese due to pasteurizer recorder chart malfunction.

Routine NY Agriculture and Markets inspection found pasteurization temperature was not recorded for two lots of cheese due to pasteurizer recorder chart malfunction.

Routine NY Agriculture and Markets inspection found pasteurization temperature was not recorded for two lots of cheese due to pasteurizer recorder chart malfunction.

product tested positive for Listeria monocytogenes

Routine NY Agriculture and Markets inspection found pasteurization temperature was not recorded for two lots of cheese due to pasteurizer recorder chart malfunction.

Aflatoxin level slightly above actionable limit

Potential to be contaminated with Salmonella

cMGP Deviations: Drug products repackaged into pouches without supporting stability studies.

CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level per manufacturer

cMGP Deviations: Drug products repackaged into pouches without supporting stability studies.

CGMP Deviations: Presence of NDMA impurity detected in product.

Failed Impurties/Degradation Specifications: out of specification results for an impurity for one lot

cMGP Deviations: Drug products repackaged into pouches without supporting stability studies.

Failed Impurities/Degradation Specifications; high out of specification results obtained at the 9 month stability timepoint

CGMP deviations; repackaged product was recalled by the manufacturer because it was manufactured under the same conditions as products found to be sub-potent.

CGMP Deviations: Presence of NDMA impurity detected in product.