RecallRadar

FDA Device recall Z-1959-2013

Disposable Temperature Probes, (sterile), Sensor diameter: 3mm/0.12 in

On 2013-08-21 the FDA classified a Class II recall of Disposable Temperature Probes, (sterile), Sensor diameter: 3mm/0.12 in by Vital Signs Devices A Ge Healthcare, citing GE Healthcare has become aware of a potential safety issue associated with the use of GE General Purpose 9 French Temperature Probe, Disposable, 400 Series [M1024229]. GEs Dispos….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1959-2013
ClassificationClass II
Statusterminated
Initiated2013-07-18
Published2013-08-21
Last updated2026-09-13 11:53 UTC
CompanyVital Signs Devices A Ge Healthcare
DistributionUS

Product

Disposable Temperature Probes, (sterile), Sensor diameter: 3mm/0.12 in; 25 units per box. Vital Signs Inc. a GE Healthcare Company, 20 Campus Road, Totowa, NJ 07512 USA, www.gehealthcare.com/vitalsigns. Continuous temperature monitoring.

Reason

GE Healthcare has become aware of a potential safety issue associated with the use of GE General Purpose 9 French Temperature Probe, Disposable, 400 Series [M1024229]. GEs Disposable General Purpose 9FR Temperature Probe M1024229 is intended for oro-esophageal and rectal use. As it pertains to esophageal placement, it has been brought to our attention that some users are inserting the probe

Identifiers

code_infoGE product number M1024229

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-1959-2013%22

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