Reported Feb 28, 2018 · Terminated
Lidocaine USP for prescription compounding, packaged in a) 25g (NDC 58597-8019-4); b) 100g (NDC 58597-8019-6); c) 500g…
American Pharmaceutical Ingredients LLC
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: American Pharmaceutical Ingredients LLC · 6650 Highland Rd Ste 302 · Waterford, MI · 48327-1665
Is this the product you have?
4 of 4 products
| # | Product as published |
|---|---|
| 1 | 25g (NDC 58597-8019-4) |
| 2 | 100g (NDC 58597-8019-6) |
| 3 | 500g (NDC 58597-8019-7) |
| 4 | 1000 (NDC 58597-8019-8), RX only, packed by American Pharmaceutical Ingredients, LLC 6650 Highland Road, Waterford, MI 48327 |
- Lot codes and dates
Lots #: a) 110215-2Exp. 09/30/2020b) 110215-1Exp. 09/30/2020082516-1Exp. 05/31/2021c) 110215-1Exp. 09/30/2020082516-1Exp. 05/31/2021d) 110215-1Exp. 09/30/2020082516-1Exp. 05/31/2021
- Amount recalled
- 74000 g
This recall covers 66 products
The agency filed one notice per product. You are reading one of them; the other 65 are below.
53 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.
This product could cause temporary or reversible health problems — stop using it.
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