Reported Oct 31, 2012 · Terminated
BiCNU (Carmustine for injection) 100 mg and Diluent Rx Only BiCNU manufactured by: Ben Venue Laboratories, Inc.…
Bristol-myers Squibb Company
High riskUsing this product could cause serious injury, illness or death — stop using it now.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: Bristol-myers Squibb Company · 1 Squibb Dr · New Brunswick, NJ · 08901
Is this the product you have?
- BiCNU (Carmustine for injection) 100 mg and
- Diluent Rx Only BiCNU manufactured byBen Venue Laboratories, Inc. Bedford
- OH 44146 Diluent manufactured byLuitpold Pharmaceuticals, Inc. Shirley
- NY 11967 Distributed byBristol-Meyers Squibb Company Princeton, NJ 08543 USA Made in USA NDC 0015-3012-18 NDC 0015-3012-60
- Lot codes and dates
8 of 8 products
Products covered by this recall # Product as published 1 (9L7003A/1803607), Exp 11/12 2 (9H4209A/1803608), Exp 01/13 3 (9H4211A/1843251), Exp 02/13 4 (0B7004A/1843251), Exp 04/13 5 (0B7005A/2011804), (0E7004A/2011804), Exp 05/13 6 (0E7006A/2055384), Exp 09/13 7 (0J7007A/2064024), (1A7005A/2064024), Exp 01/14 8 (1C7006A/2106210), Exp 04/14 - Amount recalled
- 31,481 kits
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
- PR
Why it was recalled
Stop using this product now
Superpotent (Single Ingredient) Drug: All BiCNU lots within expiration which contain carmustine vial lots manufactured by BenVenue Laboratories (BVL) are being recalled because of an overfilled vial discovered during stability testing for a single carmustine lot.
Using this product could cause serious injury, illness or death — stop using it now.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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