Tavaborole Topical solution 5%, 10 mL bottle, Rx only, Manufactured by: Zydus Lifesciences Ltd., Changodar, Ahmedabad, India…
Reason Discoloration
723 recalls, newest first
Reason Discoloration
Reason Lack of Assurance of Sterility: Potential microbial contamination of subcutaneous pellets.
Reason Labeling: Label Mix-up: The product in the bottle contains elderberry and the label failed to indicate the inclusion of elderberry as an ingredient.
Reason Presence of Particulate Matter: Particulate matter identified as glass
Reason Subpotent Drug
Reason Failed dissolution specifications: Stability testing found that the lot did not meet dissolution specifications.
Reason cGMP deviations: The recall was initiated because required receipt testing of incoming alcohol components used to manufacture the listed hand…
Reason cGMP deviations: The recall was initiated because required receipt testing of incoming alcohol components used to manufacture the listed hand…
Reason Out-of-Specification (OOS) result during the 6-month stability testing; decreased preservative concentration.
Reason cGMP deviations: the firm released and distributed product which failed total aerobic microbial count testing.
Reason Failed impurity/degradation specifications:Out of Specification result for an individual organic impurity
Reason Failed impurity/degradation specifications:Out of Specification result for an individual organic impurity
Reason CGMP Deviations: Revised interpretation of Acceptable Quality Level (AQL) results.
Reason Product Mix-up
Reason Failed Dissolution Specifications
Reason Failed Dissolution Specifications
Reason Failed Dissolution Specifications
Reason Failed Dissolution Specifications
Reason CGMP Deviations: Market complaints received for gritty texture (grainy)
Reason CGMP Deviations
Reason Subpotent Drug: Testing revealed there was no oxytocin in the IV bag.
Reason Subpotent: During long term stability testing of Levothyroxine Sodium Tablets USP for 88 mcg, the assay content was observed below the approved…
Reason Failed Dissolution Specifications.
Reason Failed Tablet/Capsule Specifications
Reason Chemical Contamination: This recall has been initiated due to elevated levels of benzene that was discovered during post consume awareness with…