Is Zinc recalled?
155 FDA recalls mention Zinc. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Zinc.
Class II · Moderate risk Ongoing
Reason Subpotent/Super-potent Product: Testing of the SPF 50 sunscreen revealed inconsistency in SPF results ranging from SPF 4, 10, 21, 26, 33, 60, 61, and…
Class II · Moderate risk Ongoing
Reason Subpotent/Super-potent Product: Testing of the SPF 50 sunscreen revealed inconsistency in SPF results ranging from SPF 4, 10, 21, 26, 33, 60, 61, and…
Class II · Moderate risk Ongoing
Reason Lack of Assurance of Sterility
Class II · Moderate risk Ongoing
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated
Reason CGMP Deviations
Class II · Moderate risk Ongoing
Reason cGMP deviations
Class II · Moderate risk Ongoing
Reason cGMP deviations
Class II · Moderate risk Ongoing
Reason cGMP deviations
Class II · Moderate risk Ongoing
Reason cGMP deviations
Class II · Moderate risk Ongoing
Reason Chemical Contamination
Class II · Moderate risk Ongoing
Reason Chemical Contamination
Class III · Low risk Terminated
Reason Labeling: Missing Label: The finished product potentially missing the labeling with the drug facts panel, bar code and directions for use.
Class II · Moderate risk Ongoing
Reason Failed stability specifications: during routine stability monitoring quality concerns were identified. Physical separation for ingredients was…
Class II · Moderate risk Ongoing
Reason Microbial Contamination of Non-Sterile Product
Class II · Moderate risk Ongoing
Reason CGMP Deviations
Class I · High risk Ongoing
Reason Microbial Contamination of Non-Sterile Products: Presence of Aspergillus Sydowii (Mold)
Class II · Moderate risk Ongoing
Reason Subpotent Drug: Product does not contain SPF that is declared on the label.
Class II · Moderate risk Ongoing
Reason Subpotent Drug: Product does not contain SPF that is declared on the label.
Class II · Moderate risk Completed
Reason CGMP Deviations: Products not manufactured under current good manufacturing practices.
Class II · Moderate risk Ongoing
Reason CGMP Deviations: Firm went out of business and could no longer continue stability studies.
Class II · Moderate risk Ongoing
Reason CGMP Deviations: Firm went out of business and could no longer continue stability studies.
Class II · Moderate risk Ongoing
Reason CGMP Deviations:
Class II · Moderate risk Terminated
Reason CGMP Deviations: products were stored outside the drug label specifications.
Class III · Low risk Terminated
Reason Failed Dissolution Specifications
Class III · Low risk Terminated
Reason Failed Dissolution Specifications