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.
2.5A slow blow fuses may have been installed in the LEEP RPECISION Generator rather than the appropriate 3.15A slow blow fuses.
CooperSurgical is recalling LEEP Precision Integrated System 120V models due to a risk of fire from incorrect fuses. This device is used for medical procedures to remove abnormal cells. If you own this equipment, stop using it immediately to prevent fire hazards.
The system uses 2.5A slow blow fuses instead of the required 3.15A fuses. This mismatch can cause overheating and potentially lead to fire during medical procedures.
Medical facilities using the LEEP Precision Integrated System 120V models are affected. Staff and patients at these facilities are at risk of fire if the device is used with incorrect fuses.
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.
Immediately stop using the LEEP Precision Integrated System 120V model LP-10-120 if you have it.
The hazard is that 2.5A slow blow fuses may have been installed instead of the required 3.15A fuses, which could cause overheating and fire.
Check for the model number LP-10-120 on the device. The product was sold starting in 2018.
Stop using it immediately and contact CooperSurgical for further instructions.
We’ve drafted a message you can send CooperSurgical to request your refund or repair — edit it as you like.
Subject: Recall Z-1840-2019 — CooperSurgical CooperSurgical Hello, I own a CooperSurgical that is covered by recall Z-1840-2019 from CooperSurgical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
