D-0513-2023 Class II Ongoing

Recalled by Preferred Pharmaceuticals, Inc. — Anaheim, CA

FDA drug recall D-0513-2023 was initiated by Preferred Pharmaceuticals, Inc. on Mar 23, 2023 and is designated Class II. Reason for recall: cGMP Deviations for the manufacturing Firm (Accord Healthcare) after their inspection. The recall status is ongoing. Affected quantity: 72 Bottles.

Recall Details

Product Type
Drugs
Report Date
Apr 12, 2023
Initiation Date
Mar 23, 2023
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
72 Bottles

Product Description

Clopidogrel Tablets USP, 75 mg, 90-count bottles, Rx only, Manufactured: Accord Healthcare, Inc., Durham, NC 27703, NDC 68788-8190-9

Reason for Recall

cGMP Deviations for the manufacturing Firm (Accord Healthcare) after their inspection.

Distribution Pattern

USA Nationwide

Code Information

Lot: E0922W, G1222E, I0922W and K3022W Exp 10/31/2023.

Source

Dataset
openFDA drug recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for D-0513-2023
openFDA file date
Nov 10, 2026
Loaded by RegDataLab
Nov 11, 2026

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

Source: openFDA record for D-0513-2023. Report a data issue: hello@regdatalab.com.