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Abbott Medical recalls Radiofrequency Grounding Pad, REF RF-DGP-L
Recalled December 18, 2019 · FDA recall Z-0664-2020 · Abbott Medical
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. · FDA Class II
Units
8940 devices
Sold at
nationwide
Description
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.
Product
Radiofrequency Grounding Pad, REF RF-DGP-L
Manufacturer(s)
Abbott Medical
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →