Key facts
| Recalling firm | GE Medical Systems Information Technologies Inc |
|---|---|
| Manufacturer | Not disclosed in the FDA record. |
| Brand name | Not disclosed in the FDA record. |
| Product description | GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL, REF #2063702-101, Product Code SS9; used in conjunction with ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) |
| Classification | Class II |
| Recall number | Z-2242-2026 |
| Report date | Not disclosed in the FDA record. |
| Status | Ongoing |
| Reason for recall | GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station). |
What this classification means
FDA classifies a recall as Class II when using the recalled product, or being exposed to it, may cause temporary or medically reversible adverse health consequences, or when the probability of serious adverse health consequences is remote. In this case, the recalling firm is GE Medical Systems Information Technologies Inc and the affected product is described in FDA's record as: GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL, REF #2063702-101, Product Code SS9; used in conjunction with ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms). FDA's stated reason for the recall is: GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central (additional items listed in FDA's full record). The recall is tracked under FDA recall number Z-2242-2026 and carries a status of Ongoing as of the most recent FDA enforcement report. This classification reflects FDA's assessment of the product defect described above, not a prediction about any specific patient outcome. FDA maintains a public enforcement report database so that consumers, physicians, and purchasers can look up the exact product identifiers involved before deciding what to do.
What consumers should do
Because this recall carries FDA's middle severity classification, anyone who has this product should stop using it and follow the recalling firm's instructions, even though serious harm is considered unlikely for this classification. Specifically, check whether the product in your possession matches the description on file with FDA -- GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL, REF #2063702-101, Product Code SS9; used in conjunction with ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) -- and the recall number Z-2242-2026. If it matches, stop using or distributing it and contact GE Medical Systems Information Technologies Inc or the point of purchase for return or replacement instructions. Retailers and distributors holding affected inventory should quarantine it and follow the firm's written recall notice.
GE Medical Systems Information Technologies Inc’s FDA history
Argus HQ has recorded 7 total FDA actions tied to GE Medical Systems Information Technologies Inc: 0 warning letters, 7 recalls, 0 approval records, and 0 Form 483 inspection citations.
Frequently asked questions
- How serious is this recall?
- FDA classifies a recall as Class II when using the recalled product, or being exposed to it, may cause temporary or medically reversible adverse health consequences, or when the probability of serious adverse health consequences is remote.
- What should someone who has this product do?
- Because this recall carries FDA's middle severity classification, anyone who has this product should stop using it and follow the recalling firm's instructions, even though serious harm is considered unlikely for this classification. Check the product against FDA's description (GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL, REF #2063702-101, Product Code SS9; used in conjunction with ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)) and recall number Z-2242-2026, then follow GE Medical Systems Information Technologies Inc's recall instructions.
- Has GE Medical Systems Information Technologies Inc had other FDA recalls or enforcement actions?
- Yes. Argus HQ has recorded 7 total FDA actions tied to GE Medical Systems Information Technologies Inc, including 7 recalls and 0 warning letters.
- What is the FDA recall number for this event?
- FDA recall number Z-2242-2026.
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Related enforcement actions
Full FDA history for GE Medical Systems Information Technologies IncCompiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder
Cite this record
Reusing this data in reporting or research? Here’s a ready-made citation.
Argus HQ Research (2026). FDA Recall Database: Class II Recall: GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL,… by GE Medical Systems Information Technologies Inc. Digital Empire LLC. Retrieved from https://argushq.ai/recall/fda-recall-ge-medical-systems-information-technologies-inc-z-2242-2026
"FDA Recall Database: Class II Recall: GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL,… by GE Medical Systems Information Technologies Inc." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/recall/fda-recall-ge-medical-systems-information-technologies-inc-z-2242-2026.
Argus HQ Research. "FDA Recall Database: Class II Recall: GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL,… by GE Medical Systems Information Technologies Inc." Digital Empire LLC. Accessed July 13, 2026. https://argushq.ai/recall/fda-recall-ge-medical-systems-information-technologies-inc-z-2242-2026.
@misc{argushq_argushq_ai_recall_fda_recall_ge_medical_systems_information_technologies_inc_z_2242_2026_2026,
title = {FDA Recall Database: Class II Recall: GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL,… by GE Medical Systems Information Technologies Inc},
author = {{Argus HQ Research}},
year = {2026},
publisher = {Digital Empire LLC},
url = {https://argushq.ai/recall/fda-recall-ge-medical-systems-information-technologies-inc-z-2242-2026},
note = {Accessed: July 13, 2026}
}Source: FDA.gov — Recalls ↗