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.
An incomplete seal at the chevron end of the primary packaging of the GLIDESHEATH SLENDER Introducer Sheath was detected in a small quantity of the affected lot population, 0.01% (1 in 10,…
Chocolate products contain undeclared milk
Undeclared milk in snack mix products
Chocolate products contain undeclared milk
Undeclared milk in snack mix products
Chocolate products contain undeclared milk
Undeclared milk in snack mix products
JLM Manufacturing LLC is recalling multiple dark chocolate products due to a supplier's recall for undeclared ingredient butterfat, and undeclared allergen milk.
The firm was informed that they did not declare soy in their ingredient statement.
JLM Manufacturing LLC is recalling multiple dark chocolate products due to a supplier's recall for undeclared ingredient butterfat, and undeclared allergen milk.
JLM Manufacturing LLC is recalling multiple dark chocolate products due to a supplier's recall for undeclared ingredient butterfat, and undeclared allergen milk.
JLM Manufacturing LLC is recalling multiple dark chocolate products due to a supplier's recall for undeclared ingredient butterfat, and undeclared allergen milk.
JLM Manufacturing LLC is recalling multiple dark chocolate products due to a supplier's recall for undeclared ingredient butterfat, and undeclared allergen milk.
Chocolate products contain undeclared milk
Undeclared milk in snack mix products
Chocolate products contain undeclared milk
Gourmet International Inc. is initiating a voluntary recall of cookie products due to undeclared colors.
Undeclared milk in snack mix products
Germack Roasting is voluntarily recalling its Dark Chocolate Almond Bark following a supplier's recall due to undeclared allergen milk.
Failed Impurities/Degradation Specifications: high out of specification test results obtained for individual and total impurities.
Microbial Contamination of Non-Sterile Products
Distribution of unapproved devices with incorrect air compression level setup
Contraindication language updated in the Instructions For Use (IFU) to indicate that Pentaray Catheters should not be used in patients with prosthetic valves.
Label on product box contains the incorrect reference #317-09 while the shelf box label with barcode and the internal foil pouch label are correctly labeled with product code 317-07 and lot…
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