Reported Jun 1, 2016 · Terminated
Auvi-Q (epinephrine injection, USP) Auto-Injector, 0.15 mg (a) 2 prefilled auto injectors + 1 trainer (NDC…
Sanofi-Aventis U.S. LLC
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: Sanofi-Aventis U.S. LLC · 55 Corporate Dr · Bridgewater, NJ · 08807-1265
Is this the product you have?
- Auvi-Q (epinephrine injection, USP) Auto-Injector, 0.15 mg (a) 2 prefilled auto injectors + 1 trainer (NDC 0024-5831-02) and (b) 1 prefilled auto injector + 1 trainer (NDC 0024-5831-00), Rx Only, Manufactured for Sanofi-Aventis US, LLC Bridgewater, NJ 08807 A Sanofi Company
- Lot codes and dates
a) 2144144exp 10/20152469674exp 04/2016250649225469782546979exp 05/201626548172654818exp 06/201626921432692144exp 07/20162719838exp 08/2016282484528910212857530exp 09/201628836312883632exp 10/2016288363329454293028243exp 11/20163037230296668029742762974280exp 12/2016and b) 2525474exp 05/2016
- Amount recalled
- 159,000 prefilled injectors
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
Defective Delivery System; potential to have inaccurate dosage delivery
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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