Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.
The newest recall records with useful source details are listed here.
Midway Specialty Vehicles, LLC dba Aunt Beths Cookies, is voluntarily recalling multiple varieties of cookies sold between January 1, 2017 and September 28, 2017, because they may contain…
Recall of Ready. Chef. Go! Seafood meal bags after notification that they were produced with vegetable products recalled by supplier for potential Listeria monocytogenes.
Pacific Coast Fruit Company, Portland, Oregon is voluntarily recalling multiple types of bagged processed salads based on the potential contamination of Listeria monocytogenes. The firm…
Midway Specialty Vehicles, LLC dba Aunt Beths Cookies, is voluntarily recalling multiple varieties of cookies sold between January 1, 2017 and September 28, 2017, because they may contain…
Stir Fry Kit product is recalled due to possible contamination with Listeria monocytogenes. The broccoli used in processing this item has been recalled by vendor Mann Packing of Salinas,…
Marketed Without An Approved NDA/ANDA: FDA analysis found this product to contain undeclared sibutramine, phenolphthalein, and n-desmethyl sibutramine, making this an unapproved drug for…
Lack Of Assurance Of Sterility.
Lack Of Assurance Of Sterility.
Failed dissolution specifications; all lots within expiry are being recalled due to out of specification dissolution results.
Lack Of Assurance Of Sterility.
Lack Of Assurance Of Sterility.
Lack Of Assurance Of Sterility.
Lack Of Assurance Of Sterility.
Subpotent Drug: low out of specification results.
Lack Of Assurance Of Sterility.
Labeling: Incorrect or Missing Package Insert: authorized generic product was packaged with the incorrect insert for the brand name product Clolar (clofarabine) injection.
Failed Impurities/Degradation Specifications: slightly elevated levels of phthalic acid.
During the review of May 2017 complaint data, a significant increase in MAX-CORE Disposable Core Biopsy Instrument complaints was observed for Failure to Prime, Failure to Fire, Failure to…
Beckman Coulter has identified that due to a PLC software nonconformity the 1K Stockyard can initiate a retrieval of a sample tube during the rack loading process, which should not occur.…
The US FDA has requested the optional energy treatment settings, "medium" and "low" (Software Protocols 02-Medium and 03-Low) be removed from all Ablatherm Integrated Imagining devices in…
Two users have reported to OriGen that a VV28F OriGen Reinforced Dual Lumen ECMO Catheter has had a separation of the clear extension tube from the hub connection. These adverse events…
There is potential that fluorescent platelet (PLT-F) and immature platelet fraction (IPF%, #) results obtained using the lots listed above may exhibit lower than actual PLT-F and IPF…
Incorrect source step size may occur in the software plans
It was reported that an implant labeled as 343-13-708 was packaged with implant 343-19-707.
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