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Terumo Medical Corporation recalls Terumo Glidesheath (tm), 6 French, Nitinol wire, product code 15-1060. Used to facilitate placing a catheter through
Recalled July 3, 2013 · FDA recall Z-1612-2013 · Terumo Medical
Hazard
Medical devices were incorrectly labeled with extended expiration dates. · FDA Class II
Units
550 units
Sold at
Nationwide Distribution.
Description
Medical devices were incorrectly labeled with extended expiration dates.
Product
Terumo Glidesheath (tm), 6 French, Nitinol wire, product code 15-1060. Used to facilitate placing a catheter through the skin into a vein or artery.
Manufacturer(s)
Terumo Medical Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →