PlainRecalls
FDA Devices Moderate Class II Terminated

Weck, Electrosurgical Coagulation Suction Tube 8 (20.0cm), 11 French, with Stylet, Teleflex Medical, Research Triangle, NC 27709. Intended to remove tissue and control bleeding by use of high-frequency electrical current.

Reported: January 22, 2014 Initiated: December 19, 2013 #Z-0771-2014

Product Description

Weck, Electrosurgical Coagulation Suction Tube 8 (20.0cm), 11 French, with Stylet, Teleflex Medical, Research Triangle, NC 27709. Intended to remove tissue and control bleeding by use of high-frequency electrical current.

Reason for Recall

Sterility cannot be guaranteed.

Details

Recalling Firm
Teleflex Medical
Units Affected
17,450 ea
Distribution
Nationwide Distribution.
Location
Research Triangle Park, NC

Frequently Asked Questions

What product was recalled?
Weck, Electrosurgical Coagulation Suction Tube 8 (20.0cm), 11 French, with Stylet, Teleflex Medical, Research Triangle, NC 27709. Intended to remove tissue and control bleeding by use of high-frequency electrical current.. Recalled by Teleflex Medical. Units affected: 17,450 ea.
Why was this product recalled?
Sterility cannot be guaranteed.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 22, 2014. Severity: Moderate. Recall number: Z-0771-2014.