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Teleflex Medical recalls RUSCH LASERTUBE (Rubber), Order No. : 102004-000060, REF 102004, SIZE I.D. mm 6,0
Recalled June 5, 2019 · FDA recall Z-1684-2019 · Teleflex Medical
Hazard
The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges. · FDA Class II
Units
4312 units
Sold at
Nationwide
Description
The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.
Product
RUSCH LASERTUBE (Rubber), Order No. : 102004-000060, REF 102004, SIZE I.D. mm 6,0
Manufacturer(s)
Teleflex Medical
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →