Reported Mar 8, 2023 · Terminated
Clopidogrel Tablets USP, 75 mg, Rx Only, Packaged in a) 30-count bottles NDC 16729-218-10 UPC 3 16729 21810 8; b)…
Accord Healthcare, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Accord Healthcare, Inc. · 1009 Slater Rd Ste 210B · Durham, NC · 27703-8446
Is this the product you have?
3 of 3 products
| # | Product as published |
|---|---|
| 1 | 30-count bottles NDC 16729-218-10 UPC 3 16729 21810 8 |
| 2 | 90-count bottles NDC 16729-218-15 UPC 3 16729 21815 3 |
| 3 | 500-count bottles, NDC 16729-218-16, UPC 3 16729 21816 0; Manufactured for: Accord Healthcare, Inc., Durham, NC 27703. Manufactured by: Intas Pharmaceuticals Limited, Pharmez, Ahmedabad-382 213, INDIA |
- Lot codes and dates
32 of 32 products
Products covered by this recall # Product as published 1 P2001925, Exp. Date 3/31/2023 2 P2003532, Exp. Date 6/30/2023 3 P2004847, Exp. Date 7/31/2023 4 R2000856, Exp. Date 11/30/2023 5 P2100452, Exp. Date 12/31/2023 6 P2100898, Exp. Date 1/31/2024 7 P2106273, Exp. Date 9/30/2024 8 R2000578, Exp. Date 7/31/2023 9 R2000653, Exp. Date 9/30/2023 10 R2000652, Exp. Date 9/30/2023 11 R2000826, Exp. Date 10/31/2023 12 R2000852, Exp. Date 10/31/2023 13 R2000853, Exp. Date 10/31/2023 14 R2000827, Exp. Date 11/30/2023 15 P2100102, Exp. Date,12/31/2023 16 P2100004, Exp. Date 12/31/2023 17 P2100450, Exp. Date 12/31/2023 18 P2100449, Exp. Date 12/31/2023 19 P2001392, P2001393, P2001395, P2001396, P2001397, P2001492, P2001493, P2001494, P2001495, Exp. Date 2/28/2023 20 P2001863, P2001864, P2001865, P2001924, P2001866, P2001926, P2001927, P2002072, P2002073, P2002071, P2002074, P2002075, P2002392, Exp. Date 3/31/2023 - Amount recalled
- 1,420,988 bottles
This recall covers 67 products
The agency filed one notice per product. You are reading one of them; the other 66 are below.
54 more are in the archive.
Where it was sold
Why it was recalled
CGMP Deviations: recalling drug products following an FDA inspection.
This product could cause temporary or reversible health problems — stop using it.
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