Western/Scott Fetzer recalls Grab n Go Opti VIPR system Model PRX-9653 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-9653 because the control knob can be rotated beyond its functional range, limiting access to flow settings. This could affect patients receiving oxygen therapy, as improper flow settings might lead to unsafe oxygen delivery.
The control knob can be rotated beyond its functional range, which limits access to flow settings. This could result in improper oxygen delivery if the device is used for emergency medical purposes. However, the device is intended for limited use and is only for emergency oxygen administration.
Patients using this oxygen delivery system for emergency medical purposes. Healthcare providers and emergency responders who administer oxygen via this device are most at risk.
This product is labeled as Grab n Go Opti VIPR system Model # PRX-9653. It was manufactured from August 31, 2014, to August 7, 2019.
Look for the model number PRX-9653 on the device label.
The device is intended for emergency use only and is safe when used by properly trained personnel for oxygen deficiency and resuscitation.
The recall does not specify a remedy, so no action is required at this time.
Yes, this device is intended for supplemental oxygen delivery for emergency medical use 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-0343-2020 — Western/Scott Fetzer Western/Scott Fetzer Hello, I own a Western/Scott Fetzer that is covered by recall Z-0343-2020 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
