EpiPen 2-Pak — Class I drug recall D-0690-2017
Ongoing recall by Meridian Medical Technologies a Pfizer Company, reported 2017-05-10, distributed nationwide. Defective Delivery System; reports of the device failing to activate which could result in a patient not recei
| Recall number | D-0690-2017 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Meridian Medical Technologies a Pfizer Company, Brentwood, MO, United States |
| Recall initiated | 2017-03-12 |
| Classified | 2017-04-28 |
| Reported by FDA | 2017-05-10 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, AT, AU, BE, CH, CL, CZ, DE, DK, EE, FI, FR, GB, HR, IE, IT, JP, LT, LV, NL, NO, NZ, PL, PT, RO, SA, SE, SG, SI, SK, TH, TW |
| NDC | 49502-0500, 49502-0500-01, 49502-0500-02, 49502-0500-92, 49502-0501, 49502-0501-01, 49502-0501-02, 49502-0501-92 |
| Lot numbers | 5FA665, 5GM631, 5GM640, 5GU763, 6FA292, 6FA293, 6GH294, 6GM072, 6GM081, 6GM082, 6GM087, 6GM088, 6GM091, 6GM198, 6GM199 |
| Expiration dates | 2017-04-20, 2017-05-20, 2017-09-20, 2017-10-20 |
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 for recall
Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0690-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.