Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported April 26, 2017
Valleylab Laparoscopic Handset; Material # E2750; Laproscopic Handset Non-Sterile Bulk; Material # E2750NSB Product Usage: For use in 5mm cannulas or larger cannulas with 5mm adapters during laparoscopic and thorascopic procedures. For use with a minimum peak voltage of 3625V.
Customer reports of the device handset continuing to operate after release of the activation button.
Covidien Medtronic recalled Valleylab Laparoscopic Handset; Material # E2750; Laproscopic Handset Non-Sterile Bulk; M… - a moderate-severity action.
Valleylab Laparoscopic Handset; Material # E2750; Laproscopic Handset Non-Sterile Bulk; M… was recalled by Covidien Medtronic in April 26, 2017. Reason: Customer reports of the device handset continuing to operate after release of the activation button.. Check the official notice for the remedy. Verify recall #Z-1836-2017 with the FDA Devices before acting.
The recall
Covidien Medtronic issued this moderate-severity FDA Devices recall-Customer reports of the device handset continuing to operate after release of the activation button..
- Moderate
- severity level
- 25K units
- affected scope
- Class II
- classification
- April 26, 2017
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1836-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1836-2017) was formally reported on April 26, 2017, with the manufacturer initiating the action on January 26, 2017. It is classified under Moderate severity (Class II), with a current status of Terminated. Covidien Medtronic is listed as the recalling firm, operating out of North Haven, CT. Federal records list the affected scope as 24,703 Units.
The documented reason for this recall is: Customer reports of the device handset continuing to operate after release of the activation button. Distribution data in the federal record shows the product reached: Worldwide - US Nationwide Distribution in the states of: AR AZ CA CO FL GA IA IL KS KY LA MA MI MN MO MS NC NE NM NY OH OR PA SC SD TN TX VA WA WV. 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
24,703 Units
Related Recalls
6
3 from same agency
Product description
Valleylab Laparoscopic Handset; Material # E2750; Laproscopic Handset Non-Sterile Bulk; Material # E2750NSB Product Usage: For use in 5mm cannulas or larger cannulas with 5mm adapters during laparoscopic and thorascopic procedures. For use with a minimum peak voltage of 3625V.
Reason for recall
Customer reports of the device handset continuing to operate after release of the activation button.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-1836-2017 |
| Date reported | April 26, 2017 |
| Date initiated | January 26, 2017 |
| Recalling firm | Covidien Medtronic |
| Firm location | North Haven, CT |
| Affected scope | 24,703 Units |
| Distribution | Worldwide - US Nationwide Distribution in the states of: AR AZ CA CO FL GA IA IL KS KY LA MA MI MN MO MS NC NE NM NY OH OR PA SC SD TN TX VA WA WV |
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-1836-2017) 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? ▼
Valleylab Laparoscopic Handset; Material # E2750; Laproscopic Handset Non-Sterile Bulk; Material # E2750NSB Product Usage: For use in 5mm cannulas or larger cannulas with 5mm adapters during laparoscopic and thorascopic procedures. For use with a minimum peak voltage of 3625V.. Recalled by Covidien Medtronic. Units affected: 24,703 Units.
Why was this product recalled? ▼
Customer reports of the device handset continuing to operate after release of the activation button.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 26, 2017. Severity: Moderate. Recall number: Z-1836-2017.
Where was the recalled product distributed? ▼
Distribution: Worldwide - US Nationwide Distribution in the states of: AR AZ CA CO FL GA IA IL KS KY LA MA MI MN MO MS NC NE NM NY OH OR PA SC SD TN TX VA WA WV.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1836-2017) 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 April 26, 2017. 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.