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FDAMarch 27, 2023device

JOURNEY II UNI XLPE TIBIA INSERT MEDIAL SZ 7-8 8MM

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

The hazard

A mispack occurred during the manufacturing process, resulting in the box incorrectly containing JOURNEY II UNI Tibia Insert Medical Size 1-2 12MM instead of the JOURNEY II UNI Tibia Insert Medial Size 7-8 8MM.

What to do

FDA enforcement status: Ongoing

Brands named

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UPCs

00885556677209

Recall history

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

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JOURNEY II UNI XLPE TIBIA INSERT MEDIAL SZ 7-8 8MM — Recall Details · AllClear