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

Not under an active recall. Cilostazol was recalled 5 times in the past — all now closed. Most recent: Nov 14, 2014.

Most common reason: Labeling / mix-up (4 of these recalls)

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

Cilostazol recalls on record

none so far in 2026; 5 on record, newest first
Class II · Moderate risk

Cilostazol active pharmaceutical ingredient packaged in varying…

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-585-2015
Class II · Moderate risk

Cilostazol

Labeling: Label Mixup: CILOSTAZOL, Tablet, 100 mg may have potentially been mislabeled as the following drug: TRIAMTERENE/ HYDROCHLOROTHIAZIDE, Tablet, 37.5 mg/25 mg, NDC 00591042401, Pedigree: W002900, EXP: 6/10/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-881-2014
Class II · Moderate risk

Cilostazol

Labeling: Label Mixup: CILOSTAZOL, Tablet, 100 mg may be potentially mislabeled as the following drug: CALCIUM ACETATE, Capsule, 667 mg, NDC 00054008826, Pedigree: W003469, EXP: 6/20/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-792-2014
Class II · Moderate risk

CILOSTAZOL Tablet

Labeling:Label Mixup; CILOSTAZOL Tablet, 100 mg may be potentially mislabeled as DUTASTERIDE, Capsule, 0.5 mg, NDC 00173071204, Pedigree: AD65475_1, EXP: 5/28/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-660-2014
Class II · Moderate risk

CILOSTAZOL Tablet

Labeling:Label Mixup; CILOSTAZOL Tablet, 100 mg may be potentially mislabeled as DUTASTERIDE, Capsule, 0.5 mg, NDC 00173071204, Pedigree: AD65475_1, EXP: 5/28/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-659-2014