Data Foundry

Drug recalls 2017

EpiPen Jr — Class I drug recall D-0691-2017

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 numberD-0691-2017
Product typeDrug
ClassificationClass I
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMeridian Medical Technologies a Pfizer Company, Brentwood, MO, United States
Recall initiated2017-03-12
Classified2017-04-28
Reported by FDA2017-05-10
DistributedNationwide (US)
Countries outside the USAR, 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
NDC49502-0500, 49502-0500-01, 49502-0500-02, 49502-0500-92, 49502-0501, 49502-0501-01, 49502-0501-02, 49502-0501-92
Lot numbers5ED824, 5GK771, 5GN767, 5GN773, 5GR765, 6ED117, 6GN215
Expiration dates2017-03-20, 2017-04-20, 2017-09-20

Product

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 AS: Epipen 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.

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-0691-2017. 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.