Product Wiki · Recalls · U.S. FDA — Device Enforcement

Stryker, T2 Guidewire, Smooth-Tipped, 2.2 x 800mm Product Usage: Intended for the temporary stabilization of bone segments or fragments. — recall Z-0880-2016

U.S. FDA — Device Enforcement · United States · 2016-01-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0880-2016
Date of alert
2016-01-21
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Stryker Howmedica Osteonics Corp.
Product category
device
Product type
Devices
Reported risk: During a review of the packaging, it was determined that the seal integrity of the pouch may be decreased.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.