Spacelabs Healthcare, Inc. recalls
Every recall we track for Spacelabs Healthcare, Inc. — 13 in all, from 2018–2026 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from Spacelabs Healthcare, Inc. peaked in 2025 (3); 13 since 2017. 8% rated “stop using now”.
All FDA recall records for Spacelabs Healthcare, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 1 | 0 | 0 | 1 |
| 2019 | 0 | 1 | 1 | 0 | 2 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 1 | 0 | 0 | 1 |
| 2023 | 0 | 1 | 0 | 0 | 1 |
| 2024 | 0 | 2 | 0 | 0 | 2 |
| 2025 | 1 | 2 | 0 | 0 | 3 |
| 2026 (to date) | 0 | 0 | 3 | 0 | 3 |
What to do if you have a recalled Spacelabs Healthcare, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Spacelabs Healthcare, Inc. recalls
11 shown- Lower riskMedical device
Spacelabs Healthcare, Inc. recalls Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102 Software Version: N/A Product
Spacelabs recalls Xhibit Central Station Model 96102 due to audio/video failures in the DisplayPort splitter component. Affected units may show distorted or no video output.
SpacelabsJun 4, 2026 - Lower riskMedical device
Spacelabs Healthcare, Inc. recalls Brand Name: Spacelabs Ultraview SL Command Module Product Name: SL Command Module Model/Catalog Number: 91496 Software
Spacelabs Healthcare recalls SL Command Module software version 91496 due to potential electrical leakage. Affected units may cause electrical hazards; contact Spacelabs for details.
SpacelabsMar 26, 2026 - Lower riskMedical device
Spacelabs Healthcare, Inc. recalls Multi-parameter Command Module, Model 91496, optioned with Masimo or Nellcor
Spacelabs Healthcare recalls Model 91496 Multi-parameter Command Modules with Masimo or Nellcor options due to potential cardiac output measurement errors that may lead to delayed care or fluid overload.
Spacelabs HealthcareFeb 27, 2026 - Use cautionMedical device
Spacelabs Healthcare, Inc. recalls Brand Name: Branding is not applied to this product. Product Name: DVI display cables Model/Catalog Number: 012-0893-01
Spacelabs Healthcare recalls DVI display cables (model 012-0893-01) that may interfere with medical devices, posing serious patient safety risks. Affected units sold with 91390/91393 monitors.
Spacelabs HealthcareSep 5, 2025 - Use cautionMedical device
Spacelabs Healthcare, Inc. recalls Xhibit Telemetry Receiver with Software, Model 96280. Intended to provide monitoring system with patient data.
Spacelabs Healthcare recalls Xhibit Telemetry Receiver software versions 1.4.0 and 1.4.1 that may cause temporary monitoring loss during system shutdowns, risking delayed clinical interventions. Affected units have specific UDI-DI codes.
Spacelabs HealthcareNov 25, 2024 - Use cautionMedical device
Spacelabs Healthcare, Inc. recalls Xhibit Telemetry Receiver, Model 96280, with Service Manual. Intended to provide monitoring system with patient data.
Spacelabs Healthcare recalls Xhibit Telemetry Receiver Model 96280 due to temporary system shutdowns causing potential delays in detecting clinical events. Affected units may lose monitoring for 1-1.5 minutes during Windows proxy issues.
Spacelabs HealthcareNov 25, 2024 - Use cautionMedical device
Spacelabs Healthcare, Inc. recalls Ultraview SL (UVSL) Command Module, Model 91496
Spacelabs Healthcare recalls UVSL Command Module Model 91496 with software versions 2.03.06 and earlier or 2.04 and later. This may cause clinicians to miss critical events due to missing alarms.
Spacelabs HealthcareApr 12, 2023 - Use cautionMedical device
Spacelabs Healthcare, Inc. recalls Xhibit Telemetry Receiver, Model: 96280
Spacelabs Healthcare recalls Xhibit Telemetry Receiver Model 96280 with software version 1.4.0 due to alarm escalation defect after 25 days of use. Caregivers may not detect technical failures.
Spacelabs HealthcareMay 31, 2022 - Use cautionMedical device
Spacelabs Healthcare, Inc. recalls Xhibit Central, Model No. 96102 - Product Usage: intended use is to provide clinicians with central monitoring of
Spacelabs Healthcare recalls Xhibit Central Model 96102 software versions 1.3.1-1.3.4 due to potential audio alarm loss after power failure or cable disconnection, which could delay recognizing patient emergencies.
Spacelabs HealthcareAug 30, 2019 - Lower riskMedical device
Spacelabs Healthcare, Inc. recalls Spacelabs Healthcare Smart Disclosure System, Model 92810, a component of the Intesys Clinical Suite (ICS) G2.
Spacelabs Healthcare recalls Model 92810 Smart Disclosure System software versions 5.00-5.03 that may print patient waveforms from another patient's records.
Spacel:labsJan 28, 2019 - Use cautionMedical device
Spacelabs Healthcare Inc recalls Spacelabs Healthcare Xhibit Telemetry Receiver, Model 96280, software version 1.1, physiological patient monitor (with
Spacelabs Healthcare recalls Model 96280 telemetry receivers with software version 1.1 due to telemetry beds dropping off the central station, causing loss of patient monitoring.
Spacelabs HealthcareJan 17, 2018
Spacelabs Healthcare, Inc. recall questions
How many recalls has Spacelabs Healthcare, Inc. had?
13 recalls from Spacelabs Healthcare, Inc. are on record with U.S. safety agencies, from 2018–2026.
What is the most recent Spacelabs Healthcare, Inc. recall?
Spacelabs Healthcare, Inc. recalls Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102 Software Version: N/A Product, dated Jun 4, 2026. Every Spacelabs Healthcare, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Spacelabs Healthcare, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Spacelabs Healthcare, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.