Stop using nowMedical device recall · FDA · Published April 23, 2019
CooperSurgical LEEP Precision System 120V Recall: Incorrect Fuses May Cause Fire
CooperSurgical recalls LEEP Precision Integrated System 120V models with potentially incorrect fuses that could lead to fire. Affected units were sold starting in 2018. Consumers should contact CooperSurgical for details.
“CooperSurgical LEEP Precision System 120V Recall: Incorrect Fuses May Cause Fire.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/68074-coopersurgical-leep-precision-system-120v-recall-incorrect-fuses-may-cause. Based on FDA recall #Z-1840-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1840-2019%22&limit=1).
CooperSurgical, Inc. recalled the LEEP Precision Integrated System 120V (Model LP-10-120) on April 23, 2019, according to the FDA. The device may contain incorrect fuses that could cause malfunction. Owners should contact CooperSurgical for a remedy.
The LEEP Precision Generator may have been installed with 2.5A slow blow fuses instead of the required 3.15A slow blow fuses, according to the FDA.
Context
GovInfoNow's records show CooperSurgical, Inc. has had 37 other recalls since October 6, 2017. Recent CooperSurgical recalls include the INCA Infant Nasal Cannulae Assy recall on August 11, 2026, and the Endosee System Convenience Kit recall on June 11, 2025. Other recent recalls of similar products include the Lutronic CLARITY II Laser System recall (January 27, 2026), the Lutronic DermaV Laser System recall (August 6, 2026), and the Olympus SOLTIVE Pro Laser System recall (February 27, 2026).
How to tell if you have this one
Check for the model number LP-10-120 on the device. The product was sold starting in 2018. The device includes a LEEP Precision Cart, Generator, and Smoke Evacuator.
Brand
CooperSurgical
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Stop using it now
Immediately stop using the LEEP Precision Integrated System 120V model LP-10-120 if you have it.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 13 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “US Nationwide Distribution in the states of CA, CT, IN, MA, MI, MN, NC, NV, NY, OH, TX, WA and WI.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: California, Connecticut, Indiana, Massachusetts, Michigan, Minnesota, Nevada, New York, North Carolina, Ohio, Texas, Washington, Wisconsin.
Recall timeline
FDA terminated this recall 12 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-1840-2019 (April 23, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1840-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 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.