Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported August 22, 2018
MegaPower Electrosurgical Generator, Product code 1000, GTIN 10614559103715
If two devices are plugged into the same channel/port in the generator, both devices activate. If one device is left laying on the patient, the result could be burning of the pati…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Megadyne Medical Products, Inc. recalled MegaPower Electrosurgical Generator, Product code 1000, GTIN 10614559103715 - a moderate-severity action.
MegaPower Electrosurgical Generator, Product code 1000, GTIN 10614559103715 was recalled by Megadyne Medical Products, Inc. in August 22, 2018. Reason: If two devices are plugged into the same channel/port in the generator, both devices activate. If one device …. Check the official notice for the remedy. Verify recall #Z-2792-2018 with the FDA Devices before acting.
The recall
Megadyne Medical Products, Inc. issued this moderate-severity FDA Devices recall-If two devices are plugged into the same channel/port in the generator, both devices activate. If one device ….
- Moderate
- severity level
- 8K units
- affected scope
- Class II
- classification
- August 22, 2018
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2792-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2792-2018) was formally reported on August 22, 2018, with the manufacturer initiating the action on May 15, 2018. It is classified under Moderate severity (Class II), with a current status of Terminated. Megadyne Medical Products, Inc. is listed as the recalling firm, operating out of Draper, UT. Federal records list the affected scope as 8380 units.
The documented reason for this recall is: If two devices are plugged into the same channel/port in the generator, both devices activate. If one device is left laying on the patient, the result could be burning of the patient. Distribution data in the federal record shows the product reached: Worldwide distribution. US Nationwide, Mexico, Europe, Middle East, Latin America, Africa, and Asia Pacific Markets. 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 - 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 - 40,422 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
8380 units
Related Recalls
6
0 from same agency
Product description
MegaPower Electrosurgical Generator, Product code 1000, GTIN 10614559103715
Reason for recall
If two devices are plugged into the same channel/port in the generator, both devices activate. If one device is left laying on the patient, the result could be burning of the patient.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-2792-2018 |
| Date reported | August 22, 2018 |
| Date initiated | May 15, 2018 |
| Recalling firm | Megadyne Medical Products, Inc. |
| Firm location | Draper, UT |
| Affected scope | 8380 units |
| Distribution | Worldwide distribution. US Nationwide, Mexico, Europe, Middle East, Latin America, Africa, and Asia Pacific Markets |
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-2792-2018) 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? ▼
MegaPower Electrosurgical Generator, Product code 1000, GTIN 10614559103715. Recalled by Megadyne Medical Products, Inc.. Units affected: 8380 units.
Why was this product recalled? ▼
If two devices are plugged into the same channel/port in the generator, both devices activate. If one device is left laying on the patient, the result could be burning of the patient.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 22, 2018. Severity: Moderate. Recall number: Z-2792-2018.
Where was the recalled product distributed? ▼
Distribution: Worldwide distribution. US Nationwide, Mexico, Europe, Middle East, Latin America, Africa, and Asia Pacific Markets.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2792-2018) 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 August 22, 2018. 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.