Reported Jul 19, 2017 · Terminated
EliquisTablets 5mg, 60 count bottle, Rx Only, Marketed by: Bristol-Meyers Squibb Company Princeton, NJ 08543 USA and…
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 · 08901-1588
Is this the product you have?
EliquisTablets 5mg60 count bottleRx Only
- Marketed by
Bristol-Meyers Squibb Company PrincetonNJ 08543 USA and Pfizer Inc. New YorkNY 10017 USANDC 0003-0894-21
- Lot codes and dates
- Lot
HN0063EXP. 09/2019
- Lot
- Amount recalled
- 48,180 bottles
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
Labeling: Label Mix-up: One bottle of Eliquis 5 mg tablet was found to contain lower-strength Eliquis 2.5 mg tablets only instead of the labeled 5 mg tablets.
Using this product could cause serious injury, illness or death — stop using it now.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Bristol-myers Squibb Company recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.