Aesculap Implant Systems LLC recalls CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM REF: PL730SU - Produ
Recalled Product
CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM REF: PL730SU - Product Usage: Instrument intended for use in general surgery and gynecologic procedures where ligation and division of vessels is desired.
Hazard / Issue
possibility of the sterility batch being insufficiently sterilized
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot # 109C and 837B
View official government recall
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