FDA Drug recall D-0690-2017
EpiPen 2-Pak (Epinephrine) Auto-Injectors 0.3 mg, Rx only, Manufactured for Mylan Specialty L.P., Morgantown WV 26505 by Meridian Medical T…
- FDA Drug
- Class I
- ongoing
- Published 2017-05-10
On 2017-05-10 the FDA classified a Class I recall of EpiPen 2-Pak (Epinephrine) Auto-Injectors 0.3 mg, Rx only, Manufactured for Mylan Specialty L.P., Morgantown WV 26505 by Meridian Medical T… by Meridian Medical Technologies A Pfizer, citing defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0690-2017 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2017-03-12 |
| Published | 2017-05-10 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Meridian Medical Technologies A Pfizer |
| Distribution | US |
Product
EpiPen 2-Pak (Epinephrine) Auto-Injectors 0.3 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 AS ---- Epipen Auto-Injector 0.3 mg -Bright Stock labeled for multiple countries- manufactured for Mylan by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company.
Reason
Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication
Identifiers
| ndc | 49502-500-01 |
|---|---|
| ndc | 49502-500-02 |
| ndc | 49502-500-92 |
| ndc | 49502-501-01 |
| ndc | 49502-501-02 |
| ndc | 49502-501-92 |
| code_info | US: lot 5GM631, exp. April 2017; lot 5GM640, exp. May 2017; lot 6GM072, exp. Sep 2017; lot 6GM082, exp. Sep 2017;…US: lot 5GM631, exp. April 2017; lot 5GM640, exp. May 2017; lot 6GM072, exp. Sep 2017; lot 6GM082, exp. Sep 2017; lot 6GM088, exp. Oct 2017; lot 6GM087, exp. Oct 2017; lot 6GM198, exp. Oct 2017; lot 6GM081, exp. Sep 2017; lot 6GM091, exp. Oct 2017; lot 6GM199, exp. Oct 2017: INTERNATIONAL: lot 5FA665, exp. April 2017; lot 5GU763, exp. May 2017; lot 6FA293, exp. Oct 2017; lot 6FA292, exp. Oct 2017; lot 6GH294, exp. Oct 2017. |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0690-2017%22
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