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

D-RAD, 1.8MM X 16MM, LOCKING PEG, QTY: (1), STERILE R, RES 74671816 Orthopedic — recall Z-1855-2017

U.S. FDA — Device Enforcement · United States · 2017-03-09 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1855-2017
Date of alert
2017-03-09
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Smith & Nephew, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
74671816
Reported risk: The expiration dates on the labeling are incorrect, the actual expiration dates are before the date on the labeling.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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