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.
The firm was notified that a specific lot of Ground Cumin Seed (lot # 2686E) they purchased had tested and found to be positive for peanut protein.
The firm was notified that a specific lot of Ground Cumin Seed (lot # 2686E) they purchased had tested and found to be positive for peanut protein.
The firm was notified that a specific lot of Ground Cumin Seed (lot # 2686E) they purchased had tested and found to be positive for peanut protein.
The firm was notified that a specific lot of Ground Cumin Seed (lot # 2686E) they purchased had tested and found to be positive for peanut protein.
The firm was notified that a specific lot of Ground Cumin Seed (lot # 2686E) they purchased had tested and found to be positive for peanut protein.
Product label does not declare milk.
The firm was notified that a specific lot of Ground Cumin Seed (lot # 2686E) they purchased had tested and found to be positive for peanut protein.
The firm was notified that a specific lot of Ground Cumin Seed (lot # 2686E) they purchased had tested and found to be positive for peanut protein.
The firm was notified that a specific lot of Ground Cumin Seed (lot # 2686E) they purchased had tested and found to be positive for peanut protein.
Simply Balanced brand White Chili dry soup mix is recalled because it was contaminated with metal shavings.
The firm was notified that a specific lot of Ground Cumin Seed (lot # 2686E) they purchased had tested and found to be positive for peanut protein.
Sun and Sands Enterprise dba Prime Time International is recalling cucumber bushels (Lot 10-1461) because they have the potential to be contaminated with Salmonella.
Labeling: Label error on declared strength. Package Insert -Error in the Description section of the package insert refers to the strength as 3mg per mL; however it should state 2mg per mL
Labeling: Label error on declared strength. Package Insert -Error in the Description section of the package insert refers to the strength as 3mg per mL; however it should state 2mg per mL
Failed Dissolution Specifications: The firm was notified that there was a dissolution out of specification result on the 6 month stability samples.
Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing firm raised concerns that the product sterility may be compromised.
Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing firm raised concerns that the product sterility may be compromised.
Labeling Not Elsewhere Classified: front labels have the incorrect NDC or 0145-1506-01 instead of the correct NDC of 0145-1506-05 and some back labels have the incorrect indication stating…
Added Instructions for Use: After application, inspect the Light Glove for barrier integrity
A complaint was received on September 27th, 2016 at a medical center in Germany for delamination and flaking of the PTFE lubricious coating on three FindrWIRZ Guidewire System .025 …
A recall was initiated by Hospira, Inc. for several lots of 5% Lidocaine HCI and 7.5% Dextrose Injection, USP, 2mL Ampul, NDC # 0409-4712-01. Some BD" Spinal Trays contain the 5% Lidocaine…
The floor locking cylinders contained in the base of the Schaerer 7300 model surgical tables were manufactured with the incorrect "O" ring which may cause the cylinder to leak.
The firm is voluntarily recalling lots of the NRG Transseptal Needle and NRG RF Transseptal Kit due to the possibility for an integrity defect to the Tyvek pouch of the NRG Transseptal…
The EP Catheters may be mislabeled for French size during reprocessing.
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