Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Clindamycin 300 mg capsules Recalled by Prescript Pharmaceuticals, Inc. Due to Labeling: Not Elsewhere Classified: due to a labeled...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Prescript Pharmaceuticals, Inc. directly.
Affected Products
Clindamycin 300 mg capsules, USP, 28-count M-Pak containers, Rx Only. Mnfct for: Lannett Co. Inc., Philadelphia, PA 19136. Mnfct. by: Lannett Co. Inc., Philadelphia, PA 19136. Pckgd by PreScript Pharm. Inc., Pleasanton, CA 94566. NDC: 00527-1383-01, Bar Code 0784-28-11
Quantity: 5 28-count containers
Why Was This Recalled?
Labeling: Not Elsewhere Classified: due to a labeled declaration of; Store at 15¿C to 30¿C (59¿F to 86¿F) which differs from the original manufacturer declaration of; Store at 20¿C to 25¿C (68¿F to 77¿F).
Where Was This Sold?
California.
About Prescript Pharmaceuticals, Inc.
Prescript Pharmaceuticals, Inc. has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report