CooperSurgical LEEP Precision Systems: Foot Pedal May Not Work Properly
CooperSurgical recalls LEEP Precision Integrated System 120V and Generator models LP-10-120 and LP-20-120 due to potential failure of cut, coagulate, or blend functions when using the foot pedal.
Lower-risk recall
The products' cut, coagulate, or blend function may not operate with the use of the Foot Pedal.
Contact the company
What happened, in plain English
CooperSurgical is recalling two medical devices: the LEEP Precision Integrated System 120V and LEEP Precision Generator models LP-10-120 and LP-20-120. The issue is that these devices may not function correctly when the foot pedal is used for cutting, coagulating, or blending procedures. Read more at govinfonow.com/recall/67654-coopersurgical-leep-precision-systems-foot-pedal-may-not-work-properly.
Source Summary by GovInfoNow · govinfonow.com/recall/67654-coopersurgical-leep-precision-systems-foot-pedal-may-not-work-properly · Updated August 20, 2026 · FDA enforcement record: FDA #Z-2057-2019
Cite this page
“CooperSurgical LEEP Precision Systems: Foot Pedal May Not Work Properly.” GovInfoNow, updated August 20, 2026. https://govinfonow.com/recall/67654-coopersurgical-leep-precision-systems-foot-pedal-may-not-work-properly. Based on FDA recall #Z-2057-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2057-2019%22&limit=1).
Why it’s dangerous
The foot pedal may not operate correctly with the cut, coagulate, or blend functions, which could lead to improper medical procedures. However, the recall does not indicate a risk of injury or serious harm in normal use.
Who’s affected
Medical professionals who use these devices for procedures like cervical or uterine treatments may be affected. The risk is low as the hazard involves potential malfunction rather than immediate injury.
How to tell if you have this one
Check for model numbers LP-10-120 or LP-20-120 on the device. The lot/serial numbers listed in the recall include many combinations from 2015 to 2017.
- Brand
CooperSurgical- Category
Medical device
What to do — step by step
Check Device Model
Identify the model number on your device to see if it matches LP-10-120 or LP-20-120.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Nationwide domestic distribution. International distribution to Canada and Costa Rica.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA terminated this recall 12 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-2057-2019 (June 18, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2057-2019 to see it in context.
- Plain-language summary written by qwen3:4b on August 20, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.