Baxter Healthcare 3,65 m Extension Set with Luer-lock Connector recall — FDA Z-1145-2022
Certain Peritoneal Dialysis product codes do not have FDA regulatory clearance and were distributed within the United States in error.
Complete FDA and NHTSA recall records dated in June 2022.
These records include useful source details for the selected month.
Certain Peritoneal Dialysis product codes do not have FDA regulatory clearance and were distributed within the United States in error.
Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty…
Anti-Kappa APC & Anti-Kappa PE analyte reagents may exhibit uncharacteristic flow profiles.
Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty…
First layer of Uniform Scanning treatment fields is sometimes irradiated with incorrect Scanning Magnet setpoints resulting in the field size may be smaller than expected and the irradiated…
A limited quantity of Cherry Coca-Cola Zero Sugar packaged in 12 oz cans were incorrectly labeled as Cherry Coca-Cola due to a mislabeling issue. Phenylalanine not declared on label.
Product Broccoli Cheddar Pasta is mislabeled as Garden Spiral Pasta and does not declare egg as an ingredient. Broccoli Cheddar Pasta has milk, egg and wheat allergens. Garden Spiral Pasta…
Undeclared milk
Undeclared milk and wheat
Undeclared milk
Undeclared milk and wheat
Products are potentially contaminated with Salmonella.
Undeclared milk
Undeclared milk
Potential to contain small pieces of stainless steel from a piece of milling equipment which was discovered during an investigative inspection of our system.
Products are potentially contaminated with Salmonella.
Undeclared milk
Products are potentially contaminated with Salmonella.
Products are potentially contaminated with Salmonella.
Undeclared milk
Undeclared milk and wheat
Superpotent Drug: product complaint for milky blue appearance and consistency, further investigation by the firm found the recalled lots out of specification for the four active ingredients.
Lack of Assurance of Sterility
Lack of Assurance of Sterility
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.