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ProCure

Twin Med, LLC · Model 1006442 · UDI-DI 10840330704479

KGB Prescription
10
510(k) clearances
175
Adverse events (6 deaths)
8
Recalls
152
Facilities

Description

ProCure Partial Rebreather Mask High Concentration w/7' Tubing 750ml ReserviorvBag Standard Connector, Partial rebreathing (no valve on mask right side for patient's using) Pediatric

Recalls

DateFirmReason
2020-11-11Westmed, Inc.There is a potential that the fitment between the oxygen delivery tube and the mask adapter may become loose. This could result in the device tubing not making a secure connection
2020-11-11Westmed, Inc.There is a potential that the fitment between the oxygen delivery tube and the mask adapter may become loose. This could result in the device tubing not making a secure connection
2020-11-11Westmed, Inc.There is a potential that the fitment between the oxygen delivery tube and the mask adapter may become loose. This could result in the device tubing not making a secure connection
2020-11-11Westmed, Inc.There is a potential that the fitment between the oxygen delivery tube and the mask adapter may become loose. This could result in the device tubing not making a secure connection
2020-11-11Westmed, Inc.There is a potential that the fitment between the oxygen delivery tube and the mask adapter may become loose. This could result in the device tubing not making a secure connection
2020-11-11Westmed, Inc.There is a potential that the fitment between the oxygen delivery tube and the mask adapter may become loose. This could result in the device tubing not making a secure connection
2004-07-12Medex IncThe non-rebreathing masks and watertraps were manufactured with natural rubber or rubber by-products and were not labeled appropriately as containinig latex.
2004-07-12Medex IncThe non-rebreathing masks and watertraps were manufactured with natural rubber or rubber by-products and were not labeled appropriately as containinig latex.

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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.