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Kardium Recalls
1 recall on record · October 17, 2012 to October 17, 2012 · Medical Devices
October 17, 2012
Medical Devices
FDA
Kardium recalls TORQ Sternal Closure Device. The common name is TWISTER, WIRE. The model number is TQ01A. The Catalog numbers are
Hazard: The TORQ Sternal Closure Device, Lot 062711, is being recalled due to probability one of the metal parts may be dislodged during use.
Kardium Recalls | RecallWatchUSA