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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.

FDA Recall Z-0275-2009 · Posted 2008-11-07

Recalling FirmHologic, Inc.
Recall StatusTerminated
Product CodeKNW
Date Initiated2008-09-22
Date Terminated2009-11-18
Product Quantity5,120 (1,024 cases of 5)

Reason for Recall

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

Firm 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.

Root Cause

Process control

Distribution Pattern

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

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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