Reported Dec 20, 2023 · Ongoing

The System is designed as a modular system with components that include an Overhead Tube Suspension with…

GE Hangwei Medical Systems, Co. Ltd.

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: GE Hangwei Medical Systems, Co. LTD · West Area Bldg. 3, No.1 Yongchang North Road · Beijing, N/A · N/A

Is this the product you have?

  • The System is designed as a modular system with components that include an Overhead Tube Suspension with tube/collimator, wallstand, Table, X-ray generator, and cleared wireless digital detectors. The list of detectors verified and validated for use with the Discovery XR656 HD system, including their specifications, are provided in the user documentation. The System generates diagnostic The components may be combined in different configurations to meet specific customer needs. In addition, upgrade configurations are available for predicate devices. The optional image pasting function enables the operator to stitch sequentially acquired radiographs into a single image. This 510(k) is to incorporate the VolumeRad advanced application that was currently available on the Discovery XR656 product onto the Discovery XR656 HD, as well as introduce a new Metal Artifact Reduction Algorithm, and an optional standalone console to take any HelixTM acquired images via DICOM (such as from a Discovery XR656 HD, Optima XR646 HD, or Optima XR240amx) and process the images independently of the system it was acquired on.
Lot codes and dates

68 of 68 products

Products covered by this recall
#Product as published
1UDI 01001952781183561122100021DX3SS2200214HLSystem ID 205620DEF1
2UDI 01001952781183561122100021DX3SS2200210HLSystem ID 602ABZSCOTTSTMPO
3UDI 01001952780702651122060021DX3SS2200096HLSystem ID 408885TEMP1
4UDI 01001952781183561122080021DX3SS2200158HLSystem ID 303827DEF1
5UDI 01001952781183561122100021DX3SS2200199HLSystem ID 561514DEF1
6UDI 01001952781183561123020021DX3SS2300053HLSystem ID 727300DEF
7UDI 01001952780702651122100021DX3SS2200194HLSystem ID 229340DEF
8UDI 01001952780702651122090021DX3SS2200173HLSystem ID 770219DEF1
9UDI 01001952780702651122090021DX3SS2200177HLSystem ID 770219DEF2
10UDI Not AvailableSystem ID 912530OPT
11UDI 01001952781183561122110021DX3SS2200243HLSystem ID 404778STKTEM1
12UDI 01001952781183561122100021DX3SS2200185HLSystem ID 208265DEF1
13UDI 01001952781183561122080021DX3SS2200141HLSystem ID NMNMHTEMP1
14UDI 01001952780702651123020021DX3SS2300054HLSystem ID NMNMHTEMP2
15UDI 01001952781183561122050021DX3SS2200071HLSystem ID 847842TEMP
16UDI 01001952781183561123060021DX3SS2300164HLSystem ID 913588TEMPO
17UDI 01001952781183561122080021DX3SS2200162HLSystem ID 337261DEF1
18UDI 01001952781183561122100021DX3SS2200189HLSystem ID 337261DEF2
19UDI 01001952780702651123040021DX3SS2300121HLSystem ID 318495DEF1
20UDI 01001952780702651123020021DX3SS2300037HLSystem ID 617SH4332
Amount recalled
68 units

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

GE HealthCare has become aware of the potential that incorrect torque has been applied to certain bolts of the Definium Tempo and Definium Tempo Pro products which may result in a potential fall of elements of the Overhead Tube Suspension (OTS) assembly.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:38 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.