FDANovember 21, 2023device

Exactech Optetrak Knee System, Catalog Numbers: a) 200-02-26, b) 200-02-29, c) 200-02-32, d) 200-02-35, e) 200-02-38, f) 200-02-41, g) 200-03-32, h) 200-07-29, i) 200-07-32, j) 200-07-35, k) 204-21-13, l) 204-22-26, m) 208-23-18, n) 208-24-13

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

The hazard

Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag.

What to do

FDA enforcement status: Ongoing

Brands named

exactech

UPCs

108858620395761088586203958310885862039590108858620396061088586203961310885862039620108858620396511088586231427710885862314284108858623142911088586204816510885862048288

Recall history

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

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