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Undeclared wheat
Finished product possibly contaminated with pathogenic Staphylococcus aureus.
Potential for external cassette leaks
A 37 mm implant width intervertebral body fusion device has a labeling discrepancy with incorrect width of 33 mm stated on the outer label side flap and inner label side flap information box. The 37 mm width on the front labels is correct.
Due to manufacturing error, digital analog rotational feature is 180 degrees off.
Downstream recall of a dietary supplement ingredient that was manufactured out of specification.
RTE fish (sushi-salmon, tuna) processed under insanitary conditions. The firm was notified by the Georgia Department of Agriculture that the products were manufactured under unsanitary conditions.
Under potency / misbranding: product fails to meet labeled lithium orotate potency. (Downstream recall) from supplier of ingredient.
4% Lithium Orotate product may only contain 3% and 9% Lithium Orotate product may contain 4.45%
Downstream recall of a dietary supplement ingredient that was manufactured out of specifications.
Failed Dissolution Specifications: Product failed to meet dissolution acceptance criteria in the stability studies at the 6th month (25¿C/60% RH) long-term.
Potential for functionality issue that supports the Over labeling feature and could lead to possible false negative results.