Reported May 10, 2017 · Ongoing
EpiPen Jr. 2-Pak (Epinephrine) Auto-Injectors 0.15 mg, Rx only, Manufactured for Mylan Specialty L.P., Morgantown WV…
Meridian Medical Technologies a Pfizer 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: Meridian Medical Technologies a Pfizer Company · 2555 Hermelin Dr · Brentwood, MO · 63144-2504
Is this the product you have?
- EpiPen Jr. 2-Pak (Epinephrine) Auto-Injectors 0.15 mg, Rx only, Manufactured for Mylan Specialty L.P., Morgantown WV 26505 by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company; NDC 49502-500-02 ----
- ALSO LABELED OUTSIDE THE US ASEpipen Auto-Injector Jr. 0.15 mg -Bright Stock labeled for multiple countries- manufactured for Mylan by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company
- Lot codes and dates
4 of 4 products
Products covered by this recall # Product as published 1 INTERNATIONAL lot 5GR765, expiration March 2017 2 lot 5GK771, expiration April 2017 3 lot 5ED824, expiration April 2017 4 and lot 6ED117, expiration *** - Amount recalled
- 92,544 2-pak (U.S.); 198,579 syringes (O.U.S.)
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
- PR
Why it was recalled
Stop using this product now
Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication
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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