Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported June 20, 2012
PlasmaJet Open Surgery Handpiece (Part of the PlasmaJet Neutral Plasma Surgery System) The PlasmaJet system is a neutral plasma surgery system that is designed for cutting and coagulation in open surgery and laparoscopic surgery.
Potential failure in the glued seal between the stem and the tip of the handpiece leading to the possible leakage of a very small drop of distilled water coolant from the handpiec…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Plasma Surgical Inc. recalled PlasmaJet Open Surgery Handpiece (Part of the PlasmaJet Neutral Plasma Surgery System) … - a moderate-severity action.
PlasmaJet Open Surgery Handpiece (Part of the PlasmaJet Neutral Plasma Surgery System) … was recalled by Plasma Surgical Inc. in June 20, 2012. Reason: Potential failure in the glued seal between the stem and the tip of the handpiece leading to the possible lea…. Check the official notice for the remedy. Verify recall #Z-1794-2012 with the FDA Devices before acting.
The recall
Plasma Surgical Inc. issued this moderate-severity FDA Devices recall-Potential failure in the glued seal between the stem and the tip of the handpiece leading to the possible lea….
- Moderate
- severity level
- 36 units
- affected scope
- Class II
- classification
- June 20, 2012
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1794-2012 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1794-2012) was formally reported on June 20, 2012, with the manufacturer initiating the action on April 27, 2012. It is classified under Moderate severity (Class II), with a current status of Terminated. Plasma Surgical Inc. is listed as the recalling firm, operating out of Roswell, GA. Federal records list the affected scope as 36 units.
The documented reason for this recall is: Potential failure in the glued seal between the stem and the tip of the handpiece leading to the possible leakage of a very small drop of distilled water coolant from the handpiece in use. Distribution data in the federal record shows the product reached: Worldwide distribution: USA (nationwide) including states of: CA and NY; and country of: United Kingdom.. 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
36 units
Related Recalls
6
3 from same agency
Product description
PlasmaJet Open Surgery Handpiece (Part of the PlasmaJet Neutral Plasma Surgery System) The PlasmaJet system is a neutral plasma surgery system that is designed for cutting and coagulation in open surgery and laparoscopic surgery.
Reason for recall
Potential failure in the glued seal between the stem and the tip of the handpiece leading to the possible leakage of a very small drop of distilled water coolant from the handpiece in use.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-1794-2012 |
| Date reported | June 20, 2012 |
| Date initiated | April 27, 2012 |
| Recalling firm | Plasma Surgical Inc. |
| Firm location | Roswell, GA |
| Affected scope | 36 units |
| Distribution | Worldwide distribution: USA (nationwide) including states of: CA and NY; and country of: United Kingdom. |
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-1794-2012) 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? ▼
PlasmaJet Open Surgery Handpiece (Part of the PlasmaJet Neutral Plasma Surgery System) The PlasmaJet system is a neutral plasma surgery system that is designed for cutting and coagulation in open surgery and laparoscopic surgery.. Recalled by Plasma Surgical Inc.. Units affected: 36 units.
Why was this product recalled? ▼
Potential failure in the glued seal between the stem and the tip of the handpiece leading to the possible leakage of a very small drop of distilled water coolant from the handpiece in use.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 20, 2012. Severity: Moderate. Recall number: Z-1794-2012.
Where was the recalled product distributed? ▼
Distribution: Worldwide distribution: USA (nationwide) including states of: CA and NY; and country of: United Kingdom..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1794-2012) 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.
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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 June 20, 2012. 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.