Class II · Moderate risk
Ampicillin 8gm in Ns 400ml
Lack of sterility assurance
Is Ampicillin recalled?
Yes — there is an active recall. 1 ongoing FDA recall mention Ampicillin (36 total). Check the affected lots below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Ampicillin. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Ampicillin recalls on record
none so far in 2026; 36 on record, newest first
Class II · Moderate risk
Ampicillin 12gm in Ns 600m
Lack of sterility assurance
Class II · Moderate risk
Ampicillin for Injection
Presence of Particulate Matter: A complaint was received for the presence of a single strand of hair in one vial.
Class II · Moderate risk
Ampicillin for Injection
cGMP deviations: Temperature abuse
Class II · Moderate risk
Unasyn (ampicillin sodium/sulbacatam)
Presence of Particulate Matter: particulate matter identified after reconstitution.
Class I · High risk
Ampicillin and Sulbactam for Injection
Presence of Particulate Matter: confirmed customer report of the presence of visible particulate matter believed to be red rubber particles from the manufacturing process of the active ingredients.
Class I · High risk
Ampicillin and Sulbactam for Injection 1.5 g vial
Presence of Particulate Matter: A confirmed customer report was received for the presence of visible particulate matter, confirmed as glass, within a single vial.
Class III · Low risk
Ampicillin for Injection
Labeling: Missing Label: customer complaint that some vials of ampicillin within the shrink wrap pack are missing labels.
Class II · Moderate risk
Ampicillin/Sulbactam 12GM in NS
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Class III · Low risk
Ampicillin Capsules
Labeling: Incorrect Or Missing Package Insert: Product is labeled with unapproved labeling.
Class II · Moderate risk
Unasyn (ampicillin/sulbactam)
Lack of Assurance of Sterility; All lots of sterile products compounded by the pharmacy within expiry are subject to this recall. This recall is initiated due to concerns associated with quality control procedures observed during a recent FDA inspection.
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