Western/Scott Fetzer recalls Grab n Go Opti VIPR system Model PRX-9627 due to limited access to flow settings from control knob rotation. This device provides supplemental oxygen for emergency use only.
Limited access to flow settings as a result of the control knob having been rotated beyond its functional range
Western/Scott Fetzer is recalling their Grab n Go Opti VIPR system model PRX-9627 because the control knob can be rotated beyond its functional range, limiting access to flow settings. This could affect patients receiving oxygen therapy by making it harder to adjust the oxygen flow rate safely.
The control knob can be rotated beyond its functional range, which limits access to flow settings. This could cause the oxygen flow rate to be set incorrectly, potentially affecting patient safety during emergency oxygen delivery.
Patients using this oxygen delivery system for emergency medical purposes, particularly those requiring supplemental oxygen during transport. Healthcare providers and emergency responders who use the device are most at risk.
This product is the Grab n Go Opti VIPR system with model number PRX-9627. It was manufactured from August 31, 2014, to August 7, 2019.
Verify the model number on the device is PRX-9627 to confirm it is affected.
The device is intended for emergency use only and is safe when used correctly by trained personnel. However, the recall indicates a potential issue with flow settings that could affect safety.
The recall does not specify a remedy, so you should check the model number and contact Western/Scott Fetzer if you need further assistance.
Yes, this device is intended for supplemental oxygen delivery in emergency medical situations, by prescription only.
We’ve drafted a message you can send Western/Scott Fetzer to request your refund or repair — edit it as you like.
Subject: Recall Z-0340-2020 — Western/Scott Fetzer Western/Scott Fetzer Hello, I own a Western/Scott Fetzer that is covered by recall Z-0340-2020 from Western/Scott Fetzer. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
