FDA Device recall Z-2179-2017
Table Patient Step on RFX/SFX, Legacy, and Precision 500D systems
- FDA Device
- Class II
- terminated
- Published 2017-06-07
On 2017-06-07 the FDA classified a Class II recall of Table Patient Step on RFX/SFX, Legacy, and Precision 500D systems by Ge Healthcare, citing reported incidents of a patient step detaching from the table. A fall from a patient step detaching while in use could result in an injury to a patient or operator.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2179-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-02-06 |
| Published | 2017-06-07 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ge Healthcare |
| Distribution | US |
Product
Table Patient Step on RFX/SFX, Legacy, and Precision 500D systems
Reason
Reported incidents of a patient step detaching from the table. A fall from a patient step detaching while in use could result in an injury to a patient or operator.
Identifiers
| code_info | FMI 10908 Initial Consignee List Mfg. Lot or Serial # System ID 00000959002WK7 907276RM4 00000966338WK6 256235ORF1…FMI 10908 Initial Consignee List Mfg. Lot or Serial # System ID 00000959002WK7 907276RM4 00000966338WK6 256235ORF1 00000966611WK6 256235ORF2 00000956387WK5 205783LRF2 00000525674WK8 205793FR1 00000964963WK3 205387LRF 964349WK5 334732SRF 00000969028WK0 205345RF3 952032WK1 501968LEG 00000510900WK4 501863MLEG 00000277058TU4 479441RF1 00000974520WK9 501321LEG1 29415VP7 928763RF 00000543656WK3 602856LEG 00000551387WK4 602994DRS 984281WK6 928537RM1 00000983374WK0 928537RM2 00000960138WK6 209386ATWRF 00000130329TX6 RADNETRF119 00000546581WK0 650696M6 00000978807WK6 818884LRF1 00000023282M37 RADNETRF1260 00000499668WK2 818331SFX 538693WK3 RADNETRF118 00000972384WK2 RADNETRF144 00000962460WK2 RADNETRF130 00000980889WK0 RADNETRF193 00000530446WK4 209225LEG2 00000531588WK2 209225LEG3 00000517706WK8 510370RFDG1 00000518141WK7 510370RFDG2 00000968783WK1 RADNETRF138 00000963491WK6 RADNETRF137 00000961786WK1 925370LMRF1 00000973156WK3 RADNETRF146 00000953812WK5 R |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2179-2017%22
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