FDA Enforcement Class II Terminated

USHER¿ Support Catheter- Angled Tip WL130cm, RI 7F; REF USH07AT; PK1022-01A; Rx only, Non-Pyrogenic, Sterile; Bard Peripheral Vascular; Manuf: FlowCardia, Inc., a Subsidiary of C. R. Bard, Inc., 745 North Pastoria Ave, Sunnyvale CA 95085. The Usher¿ Peripheral is a single lumen support catheter, with a standard luer fitting at the proximal end. The Usher¿ Peripheral is available in a length 130 cm with an angled tip shape.

Recall: Z-1529-2013 · Reported June 19, 2013

Enforcement

Recall Number
Z-1529-2013
Event ID
64276
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Bard Peripheral Vascular Inc
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
June 19, 2013
Initiation Date
January 23, 2013
Classification Date
June 10, 2013
Termination Date
June 10, 2013
Address
1625 W 3rd St Ste 109, N/A, Tempe, AZ, 85281-2438, United States

Description

USHER¿ Support Catheter- Angled Tip WL130cm, RI 7F; REF USH07AT; PK1022-01A; Rx only, Non-Pyrogenic, Sterile; Bard Peripheral Vascular; Manuf: FlowCardia, Inc., a Subsidiary of C. R. Bard, Inc., 745 North Pastoria Ave, Sunnyvale CA 95085. The Usher¿ Peripheral is a single lumen support catheter, with a standard luer fitting at the proximal end. The Usher¿ Peripheral is available in a length 130 cm with an angled tip shape.

Reason

Bard Peripheral Vascular (BPV) is initiating this recall because a combination of Bard¿ UltraClip¿ Dual Trigger Tissue Marker's and support catheters (Microsheath and Usher) were inadvertently distributed to customers without completing the sterilization process (non sterile).

Code Info

PC USH07AT; Lot# FCWC10009

Distribution

Nationwide Distribution including AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, IL, IN, KY, KS, LA, MA, MD, MI, MN, MO, MS, NC, NJ, NY, OH, OK, PA, TX, VA, WA, WV and WY.

Quantity

223