Vancomycin Hydrochloride for Injection
Reason Presence of Particulate Matter: glass particulate found in vial
Yes — there is an active recall. 22 ongoing FDA recalls mention Vancomycin (147 total). Check the affected lots below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Vancomycin. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed.
Reason Presence of Particulate Matter: glass particulate found in vial
Reason Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Reason Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Reason Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Reason Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Reason Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Reason Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Reason Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Reason Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Reason Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Reason Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Reason Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Reason Presence of Particulate Matter: A hair was found stuck to the stopper of inside a single vial. The hair came in contact with the reconstituted drug product.
Reason Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters
Reason Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Reason Presence of Particulate Matter: Cardboard
Reason Lack of Assurance of Sterility
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 Sterility Assurance
Reason Lack of Sterility Assurance.
Reason Lack of Sterility Assurance
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