Complete FDA and NHTSA recall records dated in August 2018.
These records include useful source details for the selected month.
Firm was notified by L-Leucine supplier that product may contain cyclamates. Testing of the product confirmed this and a recall was initiated.
Firm was notified by L-Leucine supplier that product may contain cyclamates. Testing of the product confirmed this and a recall was initiated.
Kauffman's Fruit Farm found high patulin levels in one lot of Apple Cider, packed in 3 different sized jugs.
Firm was notified by L-Leucine supplier that product may contain cyclamates. Testing of the product confirmed this and a recall was initiated.
Mondelez Global received notification from a supplier, Associated Milk Producers, Inc. ( AMPI ), of a voluntary recall of Whey Powder Sweet Type as a precautionary measure due to the…
Firm was notified by L-Leucine supplier that product may contain cyclamates. Testing of the product confirmed this and a recall was initiated.
Firm was notified by L-Leucine supplier that product may contain cyclamates. Testing of the product confirmed this and a recall was initiated.
Firm was notified by L-Leucine supplier that product may contain cyclamates. Testing of the product confirmed this and a recall was initiated.
Recalled whey powder was used in further production of numerous food products.
Firm was notified by L-Leucine supplier that product may contain cyclamates. Testing of the product confirmed this and a recall was initiated.
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Failed Tablet/Capsule Specifications: Tablet breakage
Failed Stability Specifications: lot out of specification for elevated water vapor.
Failed Tablet/Capsule Specifications: Tablet breakage
Superpotent Drug and Failed Stability Specifications: lot out of specification for elevated sodium chloride and elevated water vapor.
Failed Dissolution Specifications
Carcinogen impurity detected in API used to manufacture drug product.
Failed Tablet/Capsule Specifications: customer complaints of deformed, clumped, misshaped, melted or stuck together capsules.
Superpotent Drug: lots out of specification for elevated sodium chloride and fluconazole assay.
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Microbial Contamination of Sterile Products: Product associated with reports of adverse events indicative of infusion reactions related to microbiological contamination.
Failed Impurities/Degradation Specifications: An out-of-specification result in the related substance test during three month long-term stability study.
Subaru of America, Inc. (Subaru) is recalling certain 2019 Subaru Ascent vehicles. These vehicles may be missing spot welds on, or around, the B-Pillar, compromising vehicle strength.
Upon completion of a 6D workflow, the HexaPOD evo Module may be in a tilted state if it is moved to the position used for 3D (non-iGUIDE) treatments resulting in incorrect patient…
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.
