Complete FDA and NHTSA recall records dated in February 2023.
These records include useful source details for the selected month.
Select catheter lots were identified to be labeled with incorrect expiration date, where the catheters expire prior to the labeled expiration date of the kit.
The recall is due to the perforated bag not allowing for outside of the kit wrapping to be sterile, therefore, only the contents inside the kits wrapping are sterile.
The recall is due to the perforated bag not allowing for outside of the kit wrapping to be sterile, therefore, only the contents inside the kits wrapping are sterile.
Select catheter lots were identified to be labeled with incorrect expiration date, where the catheters expire prior to the labeled expiration date of the kit.
The recall is due to the perforated bag not allowing for outside of the kit wrapping to be sterile, therefore, only the contents inside the kits wrapping are sterile.
The recall is due to the perforated bag not allowing for outside of the kit wrapping to be sterile, therefore, only the contents inside the kits wrapping are sterile.
Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products label does not declare Soy Lecithin
Undeclared eggs and milk in salad
Ube cheesecake is recalled because Coconut is declared in the ingredients statement, but Coconut is not declared in the Contains statement.
Failed Dissolution Specifications: This recall is being initiated in support of the recall by the manufacturer which included lots that were packaged for BluePoint Laboratories.
Lack of sterility assurance
CGMP Deviations: initiated due to violations of CGMP manufacturing practices
Lack of sterility assurance
Lack of sterility assurance
Lack of sterility assurance
Lack of sterility assurance
Lack of sterility assurance
Lack of sterility assurance
Lack of sterility assurance
cGMP Deviation: Raw material recalled by repackager, due to discoloration of the epinephrine API.
Lack of sterility assurance
Presence of Particulate Matter: Presence of foreign substances were reported in vials at the pharmacy.
Lack of sterility assurance
Lack of sterility assurance
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.
