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3Dimensions recallZ-2168-2026 · Hologic, Inc · initiated Apr 8, 2026

Open, Classified

Is my device affected?

  1. Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
  2. If yours is listed, follow the instructions from Hologic, Inc or your healthcare provider. The company's action is summarized under what the company is doing.
  3. Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

Why it was recalled

Complaints have been received of systems developing loose, missing, or broken internal bolts over time.

FDA root cause category: Device Design

What the company is doing

On April 8, 2026 URGENT FIELD SAFETY NOTICE letters were sent to customers. Customers were informed of implementing an updated recurring maintenance inspection for detecting loosened, missing, or broken bolts within the VTA. Hologic Service will reach out to schedule your service appointment and perform the required inspection. Following the initial inspection, recurring inspections are required to be conducted at least every 6 months to ensure continued safe/proper operation of the system. Future inspections will consist of torque and visual confirmation that all bolts are present and that there is no indication of loosening. Actions: You may continue to use your 3Dimensions or Selenia Dimensions for its intended use. If at any time during system operation, you observe unexpected C-Arm movement, please discontinue use and contact Hologic s Technical Support immediately. Report suspected device complaints and/or adverse events to Hologic and the FDA (contact details below). After initial inspection by Hologic, it is required to have the inspection performed at least every 6 months as well as the other defined maintenance and service activities which are critical for continued safe and effective operation of the Selenia Dimensions or 3Dimensions system. Forward this notice to anyone in your facility that needs to be informed. Post a copy of this notice in a visible area near the affected devices where operators can view for awareness and please keep a copy for your records.

Recall details

Recall number
Z-2168-2026
Status
Open, Classified
Initiated by the company
Apr 8, 2026
Posted by the FDA
May 12, 2026
Recalling firm
Hologic, Inc
Quantity
14837 units
Product code
OTE
FDA submissions
P080003
Distribution
US Nationwide distribution.

Product description

3DIMENSIONS MAMMOGRAPHY SYSTEM; Model Numbers: 3DM-SYS-INTL2D, 3DM-SYS-INTL2D-MOB, 3DM-SYS-INTL2D-NS, 3DM-SYS-INTL3D, 3DM-SYS-INTL3D-MOB, 3DM-SYS-INTL3D-NS, 3DM-SYS-STD, 3DM-SYS-STD-MOB, 3DM-SYS-STD-NS.

Code information (models, lots, serial numbers)

"[Model No.; UDI]: [3DM-SYS-INTL2D;15420045510609], [3DM-SYS-INTL2D-MOB;15420045510593], [3DM-SYS-INTL2D-NS;15420045510586], [3DM-SYS-INTL3D;15420045510579], [3DM-SYS-INTL3D-MOB;15420045510562], [3DM-SYS-INTL3D-NS;15420045510555], [3DM-SYS-STD;15420045510524], [3DM-SYS-STD-MOB;15420045510531], [3DM-SYS-STD-NS;15420045510548]; All Serial No.

Devices named in this recall

7 devices in the FDA device registry whose identifier appears in the recall's code information.

Product lines

Other devices under the same FDA submission

8 devices cleared under P080003 are not named by identifier in this recall. One submission often covers many models, so they may or may not be affected.

Other products in the same recall event

The FDA groups related products into one recall event (event 98566).

Sources and updates

How recalls are matched to devices · Editorial policy · Report an error on this page