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

Yes — there is an active recall. 1 ongoing FDA recall mention Bromocriptine (6 total). Check the affected lots below.

Most common reason: Labeling / mix-up (3 of these recalls)

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

Bromocriptine recalls on record

none so far in 2026; 6 on record, newest first
Class II · Moderate risk

Bromocriptine Mesylate Capsules

Failed Impurities/Degradation Specifications: Out of Specification (OOS) result reported for 2- Bromoergine impurity of Bromocriptine Mesylate Capsules.

Ongoing Impurity / degradation Zydus Pharmaceuticals (USA) Inc NDC 68382-110-06 D-0159-2026
Class II · Moderate risk

Bromocriptine Mesylate Capsules USP

Failed impurities/degradation specifications: Out of specification results noticed in related substance test during analysis of 24 months long term (25 degree Celsius /65% RH) stability samples of two batches.

Terminated Impurity / degradation Zydus Pharmaceuticals USA Inc NDC 68382-110-06 D-1491-2016
Class II · Moderate risk

Bromocriptine Mesylate active pharmaceutical ingredient packaged…

Penicillin Cross Contamination: All lots of all products repackaged and distributed between 01/05/12 and 02/12/15 are being recalled because they were repackaged in a facility with penicillin products without adequate separation which could introduce the potential for cross contamination with penicillin.

Terminated Cross-contamination Attix Pharmaceuticals D-549-2015
Class II · Moderate risk

Bromocriptine Mesylate

Labeling: Label Mixup: BROMOCRIPTINE MESYLATE, Tablet, 2.5 mg may have potentially been mislabeled as one of the following drugs: BENAZEPRIL HCL, Tablet, 40 mg, NDC 65162075410, Pedigree: AD68010_1, EXP: 5/28/2014; THIORIDAZINE HCL, Tablet, 50 mg, NDC 00378061601, Pedigree: AD73525_28, EXP: 5/30/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-954-2014
Class II · Moderate risk

Bromocriptine Mesylate

Labeling: Label Mixup: BROMOCRIPTINE MESYLATE, Tablet, 2.5 mg may have potentially been mislabeled as the following drug: CAFFEINE, Tablet, 200 mg, NDC 24385060173, Pedigree: W003725, EXP: 6/26/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-953-2014
Class II · Moderate risk

Bromocriptine Mesylate

Labeling: Label Mixup: BROMOCRIPTINE MESYLATE, Tablet, 2.5 mg may have potentially been mislabeled as the following drug: CYANOCOBALAMIN, Tablet, 1000 mcg, NDC 00904421713, Pedigree: AD32582_3, EXP: 5/9/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-1011-2014