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NAR

NORTH AMERICAN RESCUE, LLC · Model 83-0036 · UDI-DI 00842209128129

POQ Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

KIT, FIELD BLOOD TRANSFUSION w/o BLOOD BAG

Recalls

Date	Firm	Reason
2020-12-23	Combat Medical Systems, LLC	There is the potential of a bent or disconnected needle in one of the components of the convenience kits.
2020-12-23	Combat Medical Systems, LLC	There is the potential of a bent or disconnected needle in one of the components of the convenience kits.
2020-12-23	Combat Medical Systems, LLC	There is the potential of a bent or disconnected needle in one of the components of the convenience kits.
2020-12-23	Combat Medical Systems, LLC	There is the potential of a bent or disconnected needle in one of the components of the convenience kits.
2020-12-23	Combat Medical Systems, LLC	There is the potential of a bent or disconnected needle in one of the components of the convenience kits.

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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.