Database updated: 3 November 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 37775 |
| Brand Name: | Hologic - Horizon W X-Ray Bone DXA Systems WI |
| Model: | Part number: Horizon-W |
| Affected: | Lot number: 308911M |
| Software version: | |
| Recalling Organisation: | Hologic (Australia and New Zealand) Pty Ltd c/o Logical Freight Solutions NZ Ltd Unit 8/113 Pavilion Drive Airport Oaks Auckland 2022 |
| Contact Information: | |
| Manufacturer: | Hologic Inc |
| Issue: | The Horizon WI systems manufactured from 11 December 2024 to 16 January 2025 were shipped without the validated VGA cables. Some installations were completed using VGA cables that may not meet Hologic's applicable performance and safety standards for this system. The impacted units may present a potential risk of elevated Electromagnetic Interference (EMI) to users and/or patients near the affected Horizon DXA systems. The impact can range from user dissatisfaction to delay in treatment and presents an elevated risk of interference to the population of individuals with active, implantable medical devices. |
| Recall action type: | Correction |
| Recall action: | Product to be exchanged |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 27/10/2026 |
