Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0020-2013 — Newport Portable Package, Model #50000, Serial # 13591, 13592, 13604, 13606, 13614, 13662, 13663, 13664, 13726, 13731, 13733, 13736, 13737, 13738, 13740, 13768, 13770, 13771, 13772, 13784, 13787. Product Usage: Portable Analgesia Gas Machine.

U.S. FDA — Device Enforcement · United States · 2012-04-29 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0020-2013
Date of alert
2012-04-29
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Accutron Inc
Product category
device
Product type
Devices
Reported risk: Accutron is recalling the Flowmeter (Analgesia Gas Machine) because when it flows Nitrous Gas without Oxygen gas being turned on, it functions in an incorrect manner.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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