Z-2230-2015 Class II Terminated

Recalled by EXP Pharmaceutical Services Corp — Fremont, CA

FDA device recall Z-2230-2015 was initiated by EXP Pharmaceutical Services Corp on February 11, 2015 and is designated Class II. Reason for recall: EXP did not register as a medical device establishment, list the devices being recalled, or establish its own quality system and instead relied on the fact that its vendors were registered and had th… The recall status is terminated (terminated December 30, 2015). Affected quantity: 1.

Recall Details

Product Type
Devices
Report Date
August 5, 2015
Initiation Date
February 11, 2015
Termination Date
December 30, 2015
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1

Product Description

Medical Device Exchange FIBERWIRE SUTURE SCISSOR; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number AR-11796; EXP (repackager), Arrow (OEM) Electrosurgical, cutting & coagulation & accessories.

Reason for Recall

EXP did not register as a medical device establishment, list the devices being recalled, or establish its own quality system and instead relied on the fact that its vendors were registered and had their own quality systems.

Distribution Pattern

Distributed in DC and the states of CO, CA, FL, TX, and AR.

Code Information

OEM Catalog number AR-11796.