Western Scott Fetzer Company Grab n Go Opti series VIPR system Model # PRX-9615 - 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 for emergency use only. For all other medical applications, the device is Rx only. The device is MR Conditional and suitable for use outside the 1,500 gauss (0.15 T) line during MR imaging for MRI syste Recall
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According to the U.S. Food and Drug Administration (FDA)
Product
Grab n Go Opti series VIPR system Model # PRX-9615 - 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 for emergency use only. For all other medical applications, the device is Rx only. The device is MR Conditional and suitable for use outside the 1,500 gauss (0.15 T) line during MR imaging for MRI syste
Brand
Western Scott Fetzer Company
Lot Codes / Batch Numbers
All Lot manufactured from 08/31/14 to 08/07/2019
Products Sold
All Lot manufactured from 08/31/14 to 08/07/2019
Western Scott Fetzer Company is recalling Grab n Go Opti series VIPR system Model # PRX-9615 - Product Usage: The Grab n Go Opti system is a due to Limited access to flow settings as a result of the control knob having been rotated beyond its functional range. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Limited access to flow settings as a result of the control knob having been rotated beyond its functional range
Recommended Action
Per FDA guidance
Western formally communicated the product issue to Praxair on 7/12/19, who had been previously in contact with Western regarding this issue. Western plans to issue a formal communication to affected distributors in the near future. The firm has initiated corrective action in the field as of August 2019. The firm has implemented a new screening process at each fill plant to identify and isolate units that could potentially be rotated past the stop. Units which fail are isolated and returned to Western, which will inspect each failed unit, replace the failed component with the revised knob/plate, and return the refurbished unit to the fill plant. One customer specifically requested that, instead of the screening procedure above, all of its units in service be replaced with the revised design. Western fulfilled this request. On October 11, 2019, Western mailed a Medical Device Recall letter to its distributors to officially communicate the issue.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026