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Emergency Medical Products

EMERGENCY MEDICAL PRODUCTS, INC. · Model DR-1 · UDI-DI 00851772007014

LMGOVRMCYOPA Prescription
0
510(k) clearances
1,755
Adverse events (27 deaths)
4
Recalls
27
Facilities

Description

Disaster Readiness Kit

Recalls

DateFirmReason
2025-11-03GET TESTED INTERNATIONAL ABDistribution without premarket approval/clearance.
2025-11-03GET TESTED INTERNATIONAL ABDistribution without premarket approval/clearance.
2024-06-11Ethicon Sarl, a Johnson & Johnson CompanySome foil pouches were found torn open, impacting the sterile barrier which was traced to a specific machine used during product packaging.
2024-06-11Ethicon Sarl, a Johnson & Johnson CompanySome foil pouches were found torn open, impacting the sterile barrier which was traced to a specific machine used during product packaging.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.