Complete FDA and NHTSA recall records dated in March 2026.
These records include useful source details for the selected month.
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an…
Uneviscerated Fish
Water was bottled under insanitary conditions.
Listeria monocytogenes
The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
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.
The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
Ingredients List declares peanut but the Contains statement does not declare peanut
Water was bottled under insanitary conditions.
The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
Potential contamination with Salmonella.
Product contains undeclared cyclamates.
Product contains undeclared cyclamates.
Water was bottled under insanitary conditions.
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
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
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
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.
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
Failed Dissolution Specifications: This recall has been initiated due to an Out of Specification finding in dissolution.
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…
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
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.
