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

Recall Z-0341-2020 — Grab n Go Opti series VIPR system Model # PRX-9632 - Product Usage: The Grab n Go Opti system is an integrated delivery system intended to provide supplemental oxygen, by Rx only, to patients. When administered by properly trained personnel for oxygen deficiency and resuscitation, the device is fo

U.S. FDA — Device Enforcement · United States · 2019-08-15 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0341-2020
Date of alert: 2019-08-15
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Western / Scott Fetzer Company
Product category: device
Product type: Devices

Reported risk: Limited access to flow settings as a result of the control knob having been rotated beyond its functional range

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.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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