FDA Recall Open, Classified

HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3

Recall: Z-2239-2026 · Initiated April 24, 2026

Recall

Recall Number
Z-2239-2026
Event Number
98843
Firm
Devicor Medical Products Inc
FEI Number
3008492462
Product Code
NEU
Status
Open, Classified
Root Cause
Labeling mix-ups
Initiated
April 24, 2026
Posted
May 27, 2026
Address
300 E Business Way, Fl 5, Cincinnati, OH, 45241-2384

Description

HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3

Reason

Incorrect inner package labeling. Boxes labeled 4010-02-15-T3 markers may contain individual packages labeled as T4 Markers.

Action

An URGENT FIELD SAFETY RECALL was sent to customers beginning 4/24/26. Action to be taken by the user: As a result of this notification, please conduct the following: "Examine your inventory and identify any devices from Lot F12607207D. "Immediately remove from use any devices labeled as 4010 02 15 T4 from this lot. "Contact your local sales representative to coordinate next steps. The affected product (devices labeled as4010 02 15 T4 from lot F12607207D) may either: -Be handed to a sales representative for removal, or -Be disposed of at your facility in accordance with local and institutional disposal requirements. "If a marker from this lot has already been implanted, review and update patient records as appropriate. "Complete and return the Recall Response Form (included with this notification), even if you no longer have affected product, to confirm the receipt of this notice and completion of required actions. If you have any additional questions, comments or concerns please contact our Customer Support at +1 877-926-2666. You may also email [email protected].

Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Singapore.

Quantity

1910 units