FDA Device

BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135412

Hazard

The affected DORADO PTA Balloon Dilatation catheters contain catheter materials that, under certain conditions, are subject to premature breakage allowing the balloon to partially or completely separate from the catheter shaft.

What You Should Do

Remedy

The Bard Peripheral Vascular "URGENT MEDICAL DEVICE RECALL NOTIFICATION" with attached "RECALL AND EFFECTIVENESS CHECK FORM" was sent to the affected consignees beginning May 7, 2010 via FedEx. The recall notice informed the consignees of the reason for recall, the products affected and instructed them not to use or further distribute any affected product. The consignees were also instructed to call the firm's Recall Coordinator Silvia Carrillo at 1-800-321-4254 Option #2 Ext 2727 (M-F 7am to 4pm MST) or email at silvia.carrillo@crbard.com to facilitate the expedient return of the affected products. Additionally they were asked to fax the Recall and Effectiveness Check Form to BPV at 1-800-994-6772.

Products

BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135412
Brand
Bard Peripheral Vascular Inc
UPC
LOT NUMBERS: 93DT0019, 93DT0050, 93DT0205, 93FT0310

Units Affected

212 units