FDA Device recall Z-0954-2015
GE Healthcare, Proteus XR/a with wall stand model number 600-0301
- FDA Device
- Class II
- terminated
- Published 2015-01-21
On 2015-01-21 the FDA classified a Class II recall of GE Healthcare, Proteus XR/a with wall stand model number 600-0301 by Ge Healthcare, citing GE Healthcare has recently become aware of a potential safety issue involving the breakage of the two steel cables which support the bucky device in the wall stand of Proteus XR/a….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0954-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-12-08 |
| Published | 2015-01-21 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Ge Healthcare |
| Distribution | US |
Product
GE Healthcare, Proteus XR/a with wall stand model number 600-0301.
Reason
GE Healthcare has recently become aware of a potential safety issue involving the breakage of the two steel cables which support the bucky device in the wall stand of Proteus XR/a X-ray imaging systems. No injuries reported.
Identifiers
| code_info | FMI 17107 - Proteus Wall Stand Counterpoise Cables Break Serial # System ID 00000044028HL9 928656ER 00000063303HL2…FMI 17107 - Proteus Wall Stand Counterpoise Cables Break Serial # System ID 00000044028HL9 928656ER 00000063303HL2 719595ORTHO 00000045940HL4 803751PR2 00000041478HL9 812238FPCRAD 00000057994HL6 208359PROT 00000046527HL8 310732TIPRO 00000047064HL1 318255PRO 00000036130HL3 319352PROT 00000053610HL2 336765WFBIRAD 00000021190HL4 360457ORTHO 00000037481HL9 405377PRO 00000031767HL7 406638CATOMO 00000034159HL4 407628PRO 00000031902HL0 409938TC1 00000074625HL5 419578RAD2 00000096491HL6 419636RAD 00000096684HL6 435563RAD 00000041757HL6 435586PROT 00000057200HL8 435658RAD 00000088306HL6 505983ORTHPROT 00000020347HL1 508698NEPATS 00000049345HL2 573882NSCRAD1 00000064320HL5 601788RAD1 00000048917HL9 601968MAERM1 00000016587HL8 602285PROT2 00000106226HL4 608366PRO 00000047063HL3 616752NWPROTEUS 00000033643HL8 623327XR3 00000059646HL0 630312PROT1 00000082840HL0 630856SCPRO 00000057436HL8 702396XR1 00000102867HL9 703771PROT 00000049772HL7 703784RAD1 00000067466HL3 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0954-2015%22
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