501 FDA recalls mention Methyl. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Methyl.
Reason Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.
Reason Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.
Reason Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.
Reason Incorrect/Undeclared Excipients.
Reason CGMP Deviations
Reason Presence of Foreign Substance: Metal embedded in a tablet.
Reason Labeling: Not Elsewhere Classified; A typographical error was observed in the NDC number on the preprinted Individual Folding Cartons (secondary…
Reason Defective Delivery System: Out of specification for shear.
Reason Defective Delivery System: Out of specification for shear.
Reason Defective Delivery System: Out of specification for shear.
Reason Defective Delivery System: Out of specification for shear.
Reason CGMP Deviations: All other lots of eye drops are being recalled due to CGMP Deviations because they were manufactured in the same facility under the…
Reason Non-Sterility: FDA analysis found unopened products to have bacterial contamination.
Reason CGMP Deviations: All other lots of eye drops are being recalled due to CGMP Deviations because they were manufactured in the same facility under the…
Reason Non-Sterility: FDA analysis found unopened products to have bacterial contamination.
Reason Lack of Assurance of Sterility
Reason Lack of sterility assurance
Reason Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Reason Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Reason Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Reason Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Reason Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Reason Defective Delivery System: Recalled lot was found to be out of specification for shear. Shear is an attribute related to the adhesive properties of…
Reason CGMP Deviations: Potential for cross contamination due to product carry over.
Reason Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the…
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