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Olympus Corporation of the Americas recalls Single Use Rotatable Clip Fixing Device Model HX 201LR 135 - Rotatable, 165cm long, 2.8 scope channel, standard clip
Recalled April 26, 2023 · FDA recall Z-1418-2023 · Olympus Corporation of the Americas
Hazard
There have been complaints that the clip did not come out of the tube sheath during the procedure. · FDA Class II
Units
65.9 boxes (373 pieces)
Sold at
US Nationwide Distribution
Description
There have been complaints that the clip did not come out of the tube sheath during the procedure.
Product
Single Use Rotatable Clip Fixing Device Model HX 201LR 135 - Rotatable, 165cm long, 2.8 scope channel, standard clip Model HX 201UR 135 - Rotatable, 230 cm long, 2.8 scope channel, standard clip Model HX 201UR 135L - Rotatable, 230 cm long, 2.8 mm scope channel, Long clip
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →