PlainRecalls

Western/Scott Fetzer Company

12 recalls on record · Latest: Apr 19, 2023

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Agency notice ledger

Federal filing book Western/Scott Fetzer Company LIGHT-BOOK · SINGLE-AGENCY

#1,309 of 14,151 · 12 notices · 0.011% archive

  • BOOK 12 notices
  • RANK #1,309 of 14,151
  • SHARE 0.011% archive
  • AGENCY FDA Devices (12)
  • CAT medical devices
  • CATS 1 category
  • LATEST Apr 19, 2023
  • PHOTO 2k Innovations Inc.

Nearest notice-volume peer: 2k Innovations Inc. (0 notice gap)

Western/Scott Fetzer Company accounts for about 0.011% of the 104,423-notice archive on 12 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Where Western/Scott Fetzer Company sits among 14,151 recalling firms

Western/Scott Fetzer Company ranks 1,309th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Western/Scott Fetzer Company vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

12 1309th of 14151 higher than 12,841 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Western/Scott Fetzer Company in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Western/Scott Fetzer Company holds about 0.011% of archive notices alongside 12 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Apr 19, 2023

Digital VIPR ROC-9839 Roberts Oxygen Ready to Use Digital VIPR (head only) ROC-9840, Roberts Oxygen Ready to Use Digital VIPR System (with E-size cylinder) MNDR-600, Western Oxytote DTE Digital VIPR (head only) MNDS-602, Western Oxytote DTE Digital VIPR System (with D-size cylinder) MNDS-603, Western Oxytote DTE Digital VIPR System (with E-size cylinder)

FDA Devices Moderate Dec 1, 2021

Western Oxytote DTE Digital VIPR System (with D-size cylinder) Model: MNDS-602

FDA Devices Moderate Dec 1, 2021

Western Oxytote DTE Digital VIPR System (with E-size cylinder) Model: MNDS-603

FDA Devices Moderate Dec 1, 2021

Western Oxytote DTE Digital VIPR (head only) Model: MNDR-600

FDA Devices Moderate Dec 1, 2021

Roberts Digital VIPR System (with E-size cylinder) Model: ROC-9840

FDA Devices Moderate Nov 13, 2019

Grab n Go Opti series VIPR system Model # PRX-9646 - 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

FDA Devices Moderate Nov 13, 2019

Grab n Go Opti series VIPR system Model # PRX-9653 - 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

FDA Devices Moderate Nov 13, 2019

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 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

FDA Devices Moderate Nov 13, 2019

Grab n Go Opti series VIPR system Model # PRX-9627 - 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

FDA Devices Moderate Nov 13, 2019

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

FDA Devices Critical Jul 29, 2015

Various OxyTOTE Portable Oxygen System regulators, Valve Integrated Pressure Regulator, one unit per package. Product Usage: Used to dispense Oxygen at prescribed flow rates to patients for therapeutic purposes and is designed to provide mobility with a self-contained supply of Oxygen.

FDA Devices Moderate Jul 2, 2014

Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR)

Western/Scott Fetzer Company holds a measurable archive slice

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Frequently Asked Questions

How many federal recall notices name Western/Scott Fetzer Company?
PlainRecalls indexes 12 distinct federal recall events naming Western/Scott Fetzer Company, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Western/Scott Fetzer Company sit among other recalling firms?
Western/Scott Fetzer Company ranks #1,309 of 14,151 by distinct recall-event count among 14,151 firms in this archive (91st percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Western/Scott Fetzer Company's notices?
FDA Devices accounts for 12 of this firm's 12 indexed notices.
What product category dominates Western/Scott Fetzer Company's filing book?
Filings for Western/Scott Fetzer Company span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous?
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Western/Scott Fetzer Company: 12 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Western/Scott Fetzer Company; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026