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

Sterile Distraction Screws of 3 different sizes: 12mm, 14mm and 16mm sold under TSI, 3COR, DB Surgical, and American Surgical Products brands and Sterile XL Screws of 7 different sizes: 90mm, 100mm, 110mm, 120mm, 130mm, 140mm, 150mm sold under TSI brand Sterile Distraction Screws are intended fo — recall Z-2385-2012

U.S. FDA — Device Enforcement · United States · 2012-06-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2385-2012
Date of alert
2012-06-11
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Tedan Surgical Innovations Llc
Product category
device
Product type
Devices
Reported risk: This letter is to notify you that several of our sterile screw products are being voluntarily recalled. Product sterility may be compromised due to a mechanical failure of the protective packaging tube. Tube end plugs may dislodge creating the potential for the screw to come out of the protective tube and then the sharp end of the screw pierce the outer sterile barrier pouch.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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