Device Recall The EnCor biopsy probe 의 리콜

Recall

60347

Class 2

Z-0351-2012

2011-11-03

2011-12-02

Terminated

United States

2012-03-29

USFDA

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=105125

This recall was voluntarily initiated by the firm due to the product 's damaged packaging trays; cracked encor (trademark) packaging trays, plastic petg tray the probe is packaged in was cracked.

The firm sent the customer notification letter on 11/07/11, via FedEx with proof of delivery notice. The letter notified customers of the reason for recall that units from the affected lot may have packaging damage resulting from transportation. The letter instructed customers to check all inventory locations , remove any identified product, to not use the affected product, and return the affected product to Bard Peripheral Vascular, Inc., 1415 W. 3rd Street, Tempe, Arizona 85281. The letter also instructed customers to fill out the recall and effectiveness check form and fax it to 1-800-894-6772. Customers were instructed to call 1-800-321-4254, Option #2 Ext 2727 for a return authorization number to facilitate the expedient return of the product. For questions regarding this recall call 480-894-9515