RecallRadar

FDA Device recall Z-2168-2026

3DIMENSIONS MAMMOGRAPHY SYSTEM

On 2026-05-20 the FDA classified a Class II recall of 3DIMENSIONS MAMMOGRAPHY SYSTEM by Hologic, citing complaints have been received of systems developing loose, missing, or broken internal bolts over time.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2168-2026
ClassificationClass II
Statusongoing
Initiated2026-04-08
Published2026-05-20
Last updated2026-09-13 11:58 UTC
CompanyHologic
DistributionUS

Product

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.

Reason

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

Identifiers

code_info
"[Model No.; UDI]: [3DM-SYS-INTL2D;15420045510609], [3DM-SYS-INTL2D-MOB;15420045510593], [3DM-SYS-INTL2D-NS;15420045510…"[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.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2168-2026%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.