FDAOctober 10, 2018device

Orthopedic Salvage System (OSS) Porous Stem, Item No. 150394

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

The hazard

Zimmer Biomet is conducting a lot specific medical device recall for two lots of the Orthopedic Salvage System (OSS) and the Comprehensive Shoulder System. The investigation determined that the Mini Humeral Stem is potentially labeled as the Bowed IM Stem lot. The associated risk of this product issue is a potential extension of surgery <30 minutes if a replacement is readily available.

What to do

FDA enforcement status: Terminated

Brands named

zimmer biometzimmer

Recall history

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

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Orthopedic Salvage System (OSS) Porous Stem, Item No. 150394 — Recall Details · AllClear