VANCOmycin 1.25 grams added to 0.9% Sodium Chloride 500 mL bag
Lack of Assurance of Sterility.
Yes — there is an active recall. 24 ongoing FDA recalls mention Vancomycin (149 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. Checked against openFDA on Oct 10, 2026.
Lack of Assurance of Sterility.
Lack of Assurance of Sterility.
Presence of Particulate Matter: glass particulate found in vial
Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
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.
Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters
Lack of Assurance of Sterility: FDA inspection identified GMP violations potentially impacting product quality and sterility.
Presence of Particulate Matter: Cardboard
Lack of Assurance of Sterility
Lack of Sterility Assurance.
Lack of Sterility Assurance
Lack of Sterility Assurance
Lack of Sterility Assurance.
Lack of Sterility Assurance.
Lack of Sterility Assurance
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