Complete FDA and NHTSA recall records dated in February 2017.
These records include useful source details for the selected month.
Product manufactured under insanitary conditions and firm did not follow the Food Code-mandated scheduled process
Failed Tablet/Capsule Specifications: customer complaints of broken or crushed capsules, resulting in loose powder in the bottle.
Subpotency: due to a low, out of specification test result for assay during stability testing.
Failed Impurities/Degradation Specifications: Product is out of specification for a known degradant.
Defective Delivery System: out of specification result for droplet size distribution at the d90 measurement testing during the 6 month time point..
Failed Tablet/Capsule Specifications: customer complaints of broken or crushed capsules, resulting in loose powder in the bottle.
Failed Dissolution Specifications; 18 month stability time point
Failed Dissolution Specifications; 18 month stability time point
Failed Tablet/Capsule Specifications: customer complaints of broken or crushed capsules, resulting in loose powder in the bottle.
Presence of Particulate Matter: Stainless steel in a chemical reactor dissolved into the API solution and was detected in the finished product.
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.
