332 FDA recalls mention Cobalamin. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Cobalamin.
Reason The firm received seven reports of adverse reactions in the form of skin abscesses potentially linked to compounded preservative-free…
Reason The firm received seven reports of adverse reactions in the form of skin abscesses potentially linked to compounded preservative-free…
Reason The firm received seven reports of adverse reactions in the form of skin abscesses potentially linked to compounded preservative-free…
Reason The firm received seven reports of adverse reactions in the form of skin abscesses potentially linked to compounded preservative-free…
Reason Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
Reason Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.
Reason Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.
Reason Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.
Reason Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.
Reason Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.
Reason Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.
Reason Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.
Reason Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.
Reason Lack of Assurance of Sterility:All sterile products compounded, repackaged, and distributed by this compounding pharmacy due to lack of sterility…
Reason Lack of Assurance of Sterility:All sterile products compounded, repackaged, and distributed by this compounding pharmacy due to lack of sterility…
Reason Lack of Assurance of Sterility: all sterile products compounded, repackaged, and distributed by this compounding pharmacy due to lack of sterility…
Reason Lack of Assurance of Sterility: all sterile products compounded, repackaged, and distributed by this compounding pharmacy due to lack of sterility…
Reason Lack of Assurance of Sterility: all sterile products compounded, repackaged, and distributed by this compounding pharmacy due to lack of sterility…
Reason Lack of Assurance of Sterility: all sterile products compounded, repackaged, and distributed by this compounding pharmacy due to lack of sterility…
Reason Lack of Assurance of Sterility; reports of adverse events after injection
Reason Lack of Assurance of Sterility; FDA inspectional findings resulted in concerns associated with quality control procedures that impacted sterility…
Reason Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
Reason Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
Reason CGMP Deviations: Pharmaceutical for injection was not manufactured according to Good Manufacturing Procedures.
Reason Non-Sterility: Green Valley Drugs received positive sterility results from their testing lab on two lots of Methylprednisolone Preservative Free 40…
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