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Arrow International Inc recalls Percutaneous Sheath Introducer Kit for use with 7 - 7.5 Fr. Catheters (8 Fr. 10 cm sheath length .035 inch dia. spring-
Recalled August 8, 2018 · FDA recall Z-2576-2018 · Arrow International
Hazard
Product contains dry natural rubber latex. Label states Latex Free. · FDA Class II
Units
60 units
Sold at
Puerto Rico
Description
Product contains dry natural rubber latex. Label states Latex Free.
Product
Percutaneous Sheath Introducer Kit for use with 7 - 7.5 Fr. Catheters (8 Fr. 10 cm sheath length .035 inch dia. spring-wire guide), REF ES-09807. The percutaneous sheath introducer permits venous access and catheter introduction to the central circulation.
Manufacturer(s)
Arrow International Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →