FDAOctober 14, 2019device

Radiofrequency Grounding Pad, REF RF-DGP-L

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

The hazard

Affected lots were manufactured with the protective release liner in an incorrect orientation. When attempting to remove this disposable release liner, a clear film may be left on the grounding pad which may interfere with patient skin contact and lead to uneven heating.

What to do

FDA enforcement status: Terminated

Brands named

abbott medicalabbott

UPCs

05415067028914

Recall history

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

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