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Recall of electrosurgery instruments ENDOPATH Probe Plus II Shaft, Ethicon

2013.05.07

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 02349/13

The company Ethicon is conducting a recall of electrosurgery instruments ENDOPATH Probe Plus II Shaft. Twelve product codes are affected. An interaction between rotation knob and the Tyvek lid could result in a sterility breach of the packaging.
The recall does not apply to the ENDOPATH Probe Plus Handles.

Recall of electrosurgery instruments ENDOPATH Probe Plus II Shaft, Ethicon , Download_VeroeffentlichtAm_EN PDF, 251KB, File does not meet accessibility standards

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