Reported Oct 7, 2015 · Terminated
Histolock Resection Device, US Endoscopy. An electrosurgical device designed to be used to endoscopically grasp,…
US Endoscopy Group Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: US Endoscopy Group Inc · 5976 Heisley Rd · Mentor, OH · 44060-1873
Is this the product you have?
- Histolock Resection Device, US Endoscopy. An electrosurgical device designed to be used to endoscopically grasp, dissect and transect tissue during gastrointestinal endoscopic procedures.
- Lot codes and dates
- M/N
00711117Lot #: 1505956
- M/N
- Amount recalled
- 41 units
Where it was sold
Why it was recalled
The company has determined the sterility cannot be assured for the affected lot.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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