Z-0216-2018 Class II Terminated

Recalled by Terumo Medical Corp — Somerset, NJ

Recall Details

Product Type
Devices
Report Date
December 20, 2017
Initiation Date
June 7, 2017
Termination Date
April 25, 2019
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
N/A

Product Description

Glidesheath Slender Hydrophilic Coated Introducer Sheath, 7FR - 10CM (0.021), REF/Product Code RM*CS7F10NA, STERILE, Rx ONLY

Reason for Recall

An incomplete seal at the chevron end of the primary packaging of the GLIDESHEATH SLENDER Introducer Sheath was detected in a small quantity of the affected lot population, 0.01% (1 in 10, 000 units). This breach of the sterile barrier may compromise the sterility of the sheath.

Distribution Pattern

Nationwide and Canada

Code Information

Lot 161111