Washington recalls

Due to battery component overheating while charging resulting in melting of internal components and causing smoke.

Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.

Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.

Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.

Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.

Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.

Software anomaly in the patient positioning system may result in positional discrepancy.

Software anomaly in the patient positioning system may result in positional discrepancy.

Potential contamination with Salmonella.

Undeclared allergen ingredient (Wheat and Sesame)

Undeclared allergen ingredient (Wheat and Sesame)

Undeclared allergen ingredient (Wheat and Sesame)

The products contain an unallowed color Carmoisine (E122) - Acid Red 14.

The products contain an unallowed color Carmoisine (E122) - Acid Red 14.

The products contain an unallowed color Carmoisine (E122) - Acid Red 14.

Listeria monocytogenes

Uneviscerated Fish

Downstream recall. Product contains arrowroot flour ingredient that was voluntarily recalled by the supplier due to potential contamination of soft kraft paper/plastic bag pieces.

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren

Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren

Labeling: Not Elsewhere Classified. The carton for Eptifibatide Injection 75 mg/100 mL states 75 mg/100 mL vial for weight-adjusted bolus dosing. The approved statement is 75 mg/100 mL vial for weight-adjusted infusion.

Failed Dissolution Specifications: This recall has been initiated due to an Out of Specification finding in dissolution.

Lack of Assurance of Sterility: due to the presence of particulate matter in one unit from the lot, which lab tests have identified as wool fiber.