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

Synthes Sciatic Nerve Retractor and Sciatic Nerve Retractor Long; Synthes Sciatic Nerve Retractor and Sciatic Nerve Retractor Long are system specific instruments to the 3.5 mm Low Profile Pelvic System Retractor Set. — recall Z-2418-2015

U.S. FDA — Device Enforcement · United States · 2015-07-29 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2418-2015
Date of alert
2015-07-29
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Synthes (USA) Products LLC
Product category
device
Product type
Devices
Reported risk: Potential for micropores to form, allowing fluid to enter the hollow handle.
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.