US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 28, 2022 (4 years ago)

Preferred Pharmaceuticals, Inc. The Physician's Solution., Lansoprazole Delayed-Release…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Out of specification results observed in dissolution during long term stability testing.

What was recalled

Preferred Pharmaceuticals, Inc. The Physician's Solution., Lansoprazole Delayed-Release Capsules, 15mg, Generic for Prevacid, 90-Count Bottle, Manufacturer: Dr Reddy's Laboratories Limited, NDC 68788-6390-09

Recalling firm
Preferred Pharmaceuticals, Inc.
NDC code
68788-6390-09
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0769-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

Other Lansoprazole recalls

See all