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Lot Recall of the Archer 0.035 inch (0.89mm) Super Stiff Guidewire, Medtronic Inc.

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 01310/13

The Medtronic Inc. recalls certain lots of Archer 0.035 inch (0.89mm) Super Stiff Guidewires from the market. The affected guidewires have the potential of kinking and breaking at the proximal weld end of the outer spring coil during in-vivo use.

Lot Recall of the Archer 0.035 inch (0.89mm) Super Stiff Guidewire, Medtronic Inc. , Download_VeroeffentlichtAm_EN PDF, 103KB, File does not meet accessibility standards