FDAMarch 21, 2023device
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 Code: PL771SU
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
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.
What to do
FDA enforcement status: Ongoing
Brands named
aesculap implant systemsaesculapaesculap implant
UPCs
04046964837340
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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