FDA Recall Terminated

ATEC Breast Biopsy and Excision System 12 gauge, 20 centimeter handpiece, sterile, Hologic, Inc., Indianapolis, IN; Model number ATEC 1212-20. Intended for partial or complete removal of tissue samples for diagnostic testing.

Recall: Z-0275-2009 · Initiated September 22, 2008

Recall

Recall Number
Z-0275-2009
Event Number
49602
Firm
Hologic, Inc.
FEI Number
3003862400
Product Code
KNW
Status
Terminated
Root Cause
Process control
Initiated
September 22, 2008
Posted
November 7, 2008
Terminated
November 18, 2009
Address
9502 Angola Ct, Ste 3, Indianapolis, IN, 46268-3178

Description

ATEC Breast Biopsy and Excision System 12 gauge, 20 centimeter handpiece, sterile, Hologic, Inc., Indianapolis, IN; Model number ATEC 1212-20. Intended for partial or complete removal of tissue samples for diagnostic testing.

Reason

The distal tip of the needle may become detached and remain in the patient, requiring surgical removal.

Action

Consignees were notified via an Urgent Medical Device Recall letter dated 9/17/08 asking them to immediately check their inventories and quarantine all affected product from the listed lots. Also, if the product had been further distributed, users were to be identified and notified of the recall. Products are to be held in quarantine until they are returned to Hologic. The response form must be completed and returned to fulfill regulatory requirements and document actions taken at your facility. Handpieces whose pouches had been opened were to be destroyed, as they could potentially shift during transport and expose dangerous sharp points to personnel handling the boxes. Upon receipt of the attached response form, Hologic will promptly send an equivalent amount of replacement product free of charge.

Distribution

Worldwide Distribution --- including USA and countries of Australia, Belgium, Brazil and Singapore.

Quantity

5,120 (1,024 cases of 5)