In the agency's Nov 18, 2026 enforcement report · Ongoing
Horizon QDR X-Ray Bone Densitometer; Models: 1. Horizon W, 2. Horizon-WI;
Hologic, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Hologic, Inc · 250 Campus Dr · Marlborough, MA · 01752-3020
Is this the product you have?
- Horizon QDR X-Ray Bone Densitometer
- Models
1. Horizon W2. Horizon-WI
- Lot codes and dates
- 1. Model Horizon W
- UDI15420045505834
- Serial Numbers
88 of 88 codes
308912M308911M308909M308908M308905M308899M308892M308890M308887M308925M308921M308918M308969M308968M308965M308964M308960M308956M308947M308945M308944M308942M308940M308939M308936M308934M308932M308928M309026M309017M309033M309029M309066M309045M309071M309048M309094M309109M309106M309104M309099M309146M309144M309136M309133M309126M309122M309117M309113M309184M309181M309177M309150M309704M309702M309700M309709M309707M309719M309715M
- UDI15420045505865
- Serial Numbers
111 of 111 codes
308848M308823M308818M308866M308862M308858M308855M308906M308902M308889M308884M309003M309002M309001M308946M308943M308941M308938M308937M308933M309008M309007M309006M309005M309004M309027M309023M309041M309037M309035M309032M309030M309069M309064M309062M309043M309039M309082M309080M309078M309076M309072M309070M309084M309187M309180M309176M309197M309196M309194M309193M309191M309189M309244M309243M309241M309240M309236M309265M309263M
- Amount recalled
- 198
Where it was sold
- Nationwide
Why it was recalled
A nonconformance was identified for systems manufactured from December 2024 to January 2025 that 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.
This product could cause temporary or reversible health problems — stop using it.
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