D-0769-2022 Class II Terminated

Recalled by Preferred Pharmaceuticals, Inc. — Anaheim, CA

FDA drug recall D-0769-2022 was initiated by Preferred Pharmaceuticals, Inc. on Mar 28, 2022 and is designated Class II. Reason for recall: Out of specification results observed in dissolution during long term stability testing. The recall status is terminated (terminated May 10, 2022). Affected quantity: 791 bottles of 90 - Count.

Recall Details

Product Type
Drugs
Report Date
Apr 20, 2022
Initiation Date
Mar 28, 2022
Termination Date
May 10, 2022
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
791 bottles of 90 - Count

Product Description

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

Reason for Recall

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

Distribution Pattern

Nationwide in the USA and CA.

Code Information

Lots: H0221R, D3021T, D2221J, D1321X, Exp.12/31/2023.

Source

Dataset
openFDA drug recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for D-0769-2022
openFDA file date
Oct 23, 2026
Loaded by RegDataLab
Oct 26, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.