3M recalls its Surgical Clipper Classic model 9602 for overheating when charged with modified sine wave inverters. This could cause fire or injury during emergency medical use.
3M has recently received reports involving the 3MTM Surgical Clipper by Remington¿, Model 9602, overheating in mobile/field EMS situations while charging from a modified sine wave power inverter.
3M is recalling its Surgical Clipper Classic model 9602 because it can overheat when charged using modified sine wave inverters. This poses a fire risk during emergency medical procedures where the clipper is used in the field.
The clipper overheats when charged using modified sine wave inverters, which are common in portable power systems for emergency medical use. This overheating can lead to fire or injury if the clipper is used in mobile or field emergency situations.
Healthcare workers using this clipper in emergency medical settings are most at risk. Patients undergoing hair removal procedures with this device could also be affected.
Check for the 3M Surgical Clipper Classic model 9602. This device is intended for removing body and head hair during medical procedures. All lots of this model are affected.
Ensure the clipper is charged using a standard power source, not a modified sine wave inverter.
If the clipper becomes unusually hot during charging, stop use immediately.
The recall specifically addresses overheating in mobile/field EMS situations using modified sine wave inverters. It may be safe for home use with standard power sources.
Check for the 3M Surgical Clipper Classic model 9602. All lots of this model are affected by the recall.
Stop using it immediately and check if it's being charged with a modified sine wave inverter.
We’ve drafted a message you can send 3M to request your refund or repair — edit it as you like.
Subject: Recall Z-0791-2019 — 3M 3M Hello, I own a 3M that is covered by recall Z-0791-2019 from 3M. 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.
