FDAOctober 26, 2016device

3M Universal Electrosurgical Pad, REF 9130 (100 pads / case) and 3M Universal Electrosurgical Pad with Cord, REF 9135-LP (40 pads / case) Product Usage: 3M Universal Electrosurgical Pads are designed to work with most electrosurgical unite (ESU) for virtually every surgical application where elec...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

3M is recalling Universal Electrosurgical Pads because a report of an unintended material (process liner) in the product. This may prevent or impede the safe return of electrosurgical current following Electrosurgical Unit (ESU) activation. This defect has the potential to increase the risk of a patient burn directly under the pad or at an alternate site of the body.

What to do

FDA enforcement status: Terminated

Brands named

3m company health care business

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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