Reported May 17, 2023 · Ongoing
Aesculap Caiman Articulating D5/360MM - An electrosurgical cutting and coagulation device for…
Aesculap Implant Systems LLC
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: Aesculap Implant Systems LLC · 3773 Corporate Pkwy · Center Valley, PA · 18034-8217
Is this the product you have?
- Aesculap Caiman Articulating D5/360MM - An electrosurgical cutting and coagulation device for cutting/coagulation/ablation during endoscopic (including laparoscopic, arthroscopic) surgery, and may in addition be intended for open surgery
- Product CodePL771SU
- Lot codes and dates
- UDI-DI04046964837340
- Lot Number52785146
- Amount recalled
- 6 pieces
Where it was sold
- Nationwide
- OH
Why it was recalled
Potential for the spring to become loose and fall out of the device, if the spring falls out during a surgical procedure, it may enter the patient's body.
This product could cause temporary or reversible health problems — stop using it.
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