Yes — there is an active recall. 62 ongoing FDA recalls mention Methyl (501 total). Check the affected lots below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Methyl. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed.
Reason cGMP Deviations: Potential product contamination with Burkholderia cepacia (B.cepacia) and Ralstonia pickettii (R. pickettii).
Reason cGMP Deviations: Potential product contamination with Burkholderia cepacia (B.cepacia) and Ralstonia pickettii (R. pickettii).
Reason CGMP Deviations: Cross Contamination with other products due to CGMP cleaning failure.
Reason CGMP Deviations: Cross Contamination with other products due to CGMP cleaning failure.
Reason CGMP Deviations: Cross Contamination with other products due to CGMP cleaning failure.
Reason CGMP Deviations: Cross Contamination with other products due to CGMP cleaning failure.
Reason CGMP Deviations: Cross Contamination with other products due to CGMP cleaning failure.
Reason Lack of assurance of sterility for injectables and solutions intended to be sterile.
Reason Lack of assurance of sterility for injectables and solutions intended to be sterile.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of Assurance of Sterility
Reason Failed Stability Specification: out of specification results for Sodium Perborate
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of Assurance of Sterility
Reason Failed Stability Specifications: An out-of-specification result was obtained during 18-month stability testing for assay.
Reason Lack of Assurance of Sterility: Inadequate processes and equipment to assure the sterility of products intended to be sterile.
Reason Lack of Assurance of Sterility: Inadequate processes and equipment to assure the sterility of products intended to be sterile.
Reason Lack of Assurance of Sterility: Inadequate processes and equipment to assure the sterility of products intended to be sterile.
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