Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Is Penicillin recalled?

Yes — there is an active recall. 3 ongoing FDA recalls mention Penicillin (16 total). Check the affected lots below.

Most common reason: Sterility / contamination (7 of these recalls)

Recalls are matched by product description. A recall usually affects specific lots, not every package of Penicillin. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.

Penicillin recalls on record

none so far in 2026; 16 on record, newest first
Class II · Moderate risk

Bicillin L-A

cGMP Deviations: Products were stored outside the drug label specifications.

Terminated Labeling / mix-up Mckesson Medical-Surgical Inc. Corporate Office NDC 60793-0701-10 D-0373-2024
Class III · Low risk

Penicillin V Potassium Tablets

Presence of Foreign Tablet/Capsule; Amoxicillin 500 mg was found in bottles of Penicillin V potassium 500 mg

Terminated Cross-contamination Citron Pharma Llc NDC 57237-041-99 D-0652-2017
Class II · Moderate risk

Peng/proc/strep/chlor/hyos

Lack of Assurance of Sterility: Martin Avenue Pharmacy, Inc. is conducting a voluntary recall of all compounded sterile preparations within expiry. The recall is being initiated in connection with a recent FDA inspection due to observations associated with certain quality control procedures that present a risk to sterility assurance.

Terminated Sterility / contamination Martin Avenue Pharmacy, Inc. D-0110-2015
Class II · Moderate risk

Pfizerpen (penicillin G)

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.

Ongoing Sterility / contamination Franck's Lab Inc dba Trinity Care Solutions D-1455-2014
Class II · Moderate risk

Penicillin G Potassium 10

Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all Sterile Human Drugs distributed between 11/21/2011 and 05/21/2012. FDA environmental sampling revealed the presence of microorganisms and fungal growth in the clean room where sterile products were prepared.

Terminated Sterility / contamination Franck's Lab Inc., d.b.a. Franck's Compounding Lab D-1596-2012