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Aesculap Implant Systems LLC recalls CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM REF: PL730SU - Product Usage: Instrument intended for use in general surgery and
Recalled September 18, 2019 · FDA recall Z-2496-2019 · Aesculap Implant Systems
Hazard
possibility of the sterility batch being insufficiently sterilized · FDA Class II
Units
3 unit of Lot 837B
Sold at
US Nationwide distribution in the state of CA.
Description
possibility of the sterility batch being insufficiently sterilized
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.
Manufacturer(s)
Aesculap Implant Systems LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →