Medical device recalls Moderate risk

Synthes (USA) Products LLC recalls Extraction Hook - Sterile for TI Cannulated Nails

Recall date
October 3, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0642-2017
FDA classification
Class II
Brand / firm
Synthes (USA) Products LLC
Sold / distributed
Distributed Nationwide

Why it was recalled

The peel pouches for the affected reaming rods and extraction hooks are delaminating.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Extraction Hook - Sterile for TI Cannulated Nails

Get recall alerts

Free email alert whenever Synthes (USA) Products LLC has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: Synthes (USA) Products LLC