FDA Recall Open, Classified

microTargeting Insertion Tube Set, P/N 66-IT-05P, Lot 244517. The intended use is to accurately guide a microelectrode or instrument in the brain during stereotactic functional neurosurgical procedures.

Recall: Z-0312-2025 · Initiated October 4, 2024

Recall

Recall Number
Z-0312-2025
Event Number
95479
Firm
FHC, Inc.
FEI Number
3002250546
Product Code
HAW
Status
Open, Classified
Root Cause
Process change control
Initiated
October 4, 2024
Posted
November 8, 2024
Address
1201 Main St, Bowdoin, ME, 04287-7302

Description

microTargeting Insertion Tube Set, P/N 66-IT-05P, Lot 244517. The intended use is to accurately guide a microelectrode or instrument in the brain during stereotactic functional neurosurgical procedures.

Reason

A complaint was received (MDR 3002250546-2024-00003) prompting an investigation. The investigation revealed a schematic for a spacer tube which is too long relative to the size of other components was included in the build order for Lot 244517 of P/N 66-IT-06P. Use of the product with a spacer tube which is too long could result in intercranial hemorrhaging and brain damage.

Action

On October 4, 2024, the firm notified affected consignees via Urgent Medical Device Recall letters. Customers were instructed to immediately identify and quarantine all affected product. The firm will contact customers and issue an RMA to return affected product and issue a replacement by 10/11/24. Customers should not use the product in the interim. Should you have any further questions regarding this matter you may contact the firm by email at [email protected] or by telephone at 207-666-5425.

Distribution

Domestic distribution only to the following states: AZ, CA, PA, TN, TX, WA.

Quantity

8 packs of 5ea (40 total)