Z-1791-2020 Class I Terminated

Recalled by Argon Medical Devices, Inc — Athens, TX

Recall Details

Product Type
Devices
Report Date
May 13, 2020
Initiation Date
December 4, 2019
Termination Date
April 1, 2024
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1690 units

Product Description

0.035"(.89mm)x80 cm guidewire. Model 114135080. Soft Tip 3.5cm. REF/UDI: 114135080/(01)208863333008067. RxOnly STERILE EO

Reason for Recall

The stiffness of the soft end of the guidewire caused tissue perforation.

Distribution Pattern

No US consignees. OUS - Sweden, Norway, Denmark, Greece, Slovenia, Turkey, Hong Kong, England

Code Information

Guidewire Model 114135080; LOT numbers: 11235895, 11234476, 11237014, and 11240602.