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Teleflex Medical recalls Pilling Modular Verres Body/Obturator, Product Code 140880
Recalled March 23, 2016 · FDA recall Z-1178-2016 · Teleflex Medical
Hazard
Packaging error in which customers who ordered product code 140880 (Verres cannula for use with a separately available needle tip) were incorrectly provided with product code 140878 (Verres cannula with integral needle tip). · FDA Class II
Units
8
Sold at
US Distribution to the state of : UT
Description
Packaging error in which customers who ordered product code 140880 (Verres cannula for use with a separately available needle tip) were incorrectly provided with product code 140878 (Verres cannula with integral needle tip).
Product
Pilling Modular Verres Body/Obturator, Product Code 140880
Manufacturer(s)
Teleflex Medical
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →