Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported July 2, 2014
Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR)
Separation events have occurred, including the VIPR separating from the Aluminum cylinder.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Western / Scott Fetzer Company recalled Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR) - a moderate-severity action.
Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR) was recalled by Western / Scott Fetzer Company in July 2, 2014. Reason: Separation events have occurred, including the VIPR separating from the Aluminum cylinder.. Check the official notice for the remedy. Verify recall #Z-1849-2014 with the FDA Devices before acting.
The recall
Western / Scott Fetzer Company issued this moderate-severity FDA Devices recall-Separation events have occurred, including the VIPR separating from the Aluminum cylinder..
- Moderate
- severity level
- 118K units
- affected scope
- Class II
- classification
- July 2, 2014
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1849-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1849-2014) was formally reported on July 2, 2014, with the manufacturer initiating the action on April 7, 2014. It is classified under Moderate severity (Class II), with a current status of Terminated. Western / Scott Fetzer Company is listed as the recalling firm, operating out of Westlake, OH. Federal records list the affected scope as 118,325 units, a scale large enough to require multi-state distribution tracking.
The documented reason for this recall is: Separation events have occurred, including the VIPR separating from the Aluminum cylinder. Distribution data in the federal record shows the product reached: Worldwide Distribution-USA (nationwide) including Puerto Rico and the states of Alaska, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Kansas, Kentuck…. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
118,325 units
Related Recalls
6
3 from same agency
Product description
Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR)
Reason for recall
Separation events have occurred, including the VIPR separating from the Aluminum cylinder.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-1849-2014 |
| Date reported | July 2, 2014 |
| Date initiated | April 7, 2014 |
| Recalling firm | Western / Scott Fetzer Company |
| Firm location | Westlake, OH |
| Affected scope | 118,325 units |
| Distribution | Worldwide Distribution-USA (nationwide) including Puerto Rico and the states of Alaska, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massac… |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-1849-2014) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR). Recalled by Western / Scott Fetzer Company. Units affected: 118,325 units.
Why was this product recalled? ▼
Separation events have occurred, including the VIPR separating from the Aluminum cylinder.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 2, 2014. Severity: Moderate. Recall number: Z-1849-2014.
Where was the recalled product distributed? ▼
Distribution: Worldwide Distribution-USA (nationwide) including Puerto Rico and the states of Alaska, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, and West Virginia and the countries of Canada,China, Costa Rica, France, Honduras, India, Ireland, Italy, Japan, Korea (South), Malaysia, Panama, Spain and Taiwan..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1849-2014) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nearby Recalls in This Category
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported July 2, 2014. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.