FDAMay 22, 2018device

ADVANSYS MLP/DLP, Model Numbers: 181051S, 181052S, 181041S, 181042S, 181031S, 181032S, 181033S, 181021S, 181022S & 181023S

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

The hazard

Use of the impacted product may cause a superficial infection requiring PO antibiotics and wound care or deep infection requiring IV antibiotics and device removal.

What to do

FDA enforcement status: Terminated

Brands named

newdeal sanewdeal

Recall history

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

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