--- title: "Spacelabs Healthcare, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Spacelabs Healthcare, Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/spacelabs-healthcare-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Spacelabs Healthcare, Inc. recall records **10** reported ongoing 10 records in this archive. Latest source date Jun 4, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Jun 4, 2026 FDA device enforcement ### [Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102 Software Version: N/A Product Description: The Spacelabs Healthcare (Spacelabs) Xhibit Centra...](https://isitonrecall.com/recall/fda-device-z-2916-2026-brand-name-xhibit-product-name-xhibit-central-station-model-catalog-number-96102-software-version-n/) Due to off-the-shelf display port component that has audio/video failures Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of AK, AL, AR, AZ, CA, CO, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, N... [Official source for Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102 Software Vers...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2916-2026%22) Mar 26, 2026 FDA device enforcement ### [Brand Name: Spacelabs Ultraview SL Command Module Product Name: SL Command Module Model/Catalog Number: 91496 Software Version: N/A Product Description: The Command Module (9149...](https://isitonrecall.com/recall/fda-device-z-2052-2026-brand-name-spacelabs-ultraview-sl-command-module-product-name-sl-command-module-model-catalog-number/) Due to a manufacturing issue (i.e. malfunctioning of electrical Leakage tester). Class II Reported ongoing Distribution: Worldwide - US Nationwide di GA, KS, MI, OH, SC, TX, WA and the country of ARGENTINA. [Official source for Brand Name: Spacelabs Ultraview SL Command Module Product Name: SL Command Module Model/Catalog N...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2052-2026%22) Feb 27, 2026 FDA device enforcement ### [Multi-parameter Command Module, Model 91496, optioned with Masimo or Nellcor](https://isitonrecall.com/recall/fda-device-z-1793-2026-multi-parameter-command-module-model-91496-optioned-with-masimo-or-nellcor/) Multi-parameter command module has a circuit board issue and when in Auto mode, Cardiac Output (CO) measurement may activate early, resulting in Bad Curve error with no CO measurement or Irregular Curve error with CO measurement not automatically excluded, ... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of NY, NJ, AL, OK, IA, MT, WY, MN, TX, WI, PA, WA, OR, MI, CA, SC, ID, FL, MS, KS, SD, LA, OH, MO, NH, GA, MD, TN,... [Official source for Multi-parameter Command Module, Model 91496, optioned with Masimo or Nellcor](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1793-2026%22) Sep 5, 2025 FDA device enforcement ### [Brand Name: Branding is not applied to this product. Product Name: DVI display cables Model/Catalog Number: 012-0895-01 Software Version: N/A Product Description: 6 foot DVI-I t...](https://isitonrecall.com/recall/fda-device-z-0167-2026-brand-name-branding-is-not-applied-to-this-product-product-name-dvi-display-cables-model-catalog-num/) Due to display cables used for monitors were not in compliance with electromagnetic interference from inadequately shielded cables which may pose serious risk to patient's safety by interfering with the operation of another electronically sensitive medical ... Class II Reported ongoing Distribution: Worldwide - United States Nationwide distribution including in the states of AK, AL, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ... [Official source for Brand Name: Branding is not applied to this product. Product Name: DVI display cables Model/Catal...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0167-2026%22) Sep 5, 2025 FDA device enforcement ### [Brand Name: Branding is not applied to this product. Product Name: DVI display cables Model/Catalog Number: 012-0895-12 Software Version: N/A Product Description: 12 foot DVI-I ...](https://isitonrecall.com/recall/fda-device-z-0168-2026-brand-name-branding-is-not-applied-to-this-product-product-name-dvi-display-cables-model-catalog-num/) Due to display cables used for monitors were not in compliance with electromagnetic interference from inadequately shielded cables which may pose serious risk to patient's safety by interfering with the operation of another electronically sensitive medical ... Class II Reported ongoing Distribution: Worldwide - United States Nationwide distribution including in the states of AK, AL, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ... [Official source for Brand Name: Branding is not applied to this product. Product Name: DVI display cables Model/Catal...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0168-2026%22) Sep 5, 2025 FDA device enforcement ### [Brand Name: Branding is not applied to this product. Product Name: DVI display cables Model/Catalog Number: 012-0893-01 Software Version: N/A Product Description: 16 inch DVI-I ...](https://isitonrecall.com/recall/fda-device-z-0169-2026-brand-name-branding-is-not-applied-to-this-product-product-name-dvi-display-cables-model-catalog-num/) Due to display cables used for monitors were not in compliance with electromagnetic interference from inadequately shielded cables which may pose serious risk to patient's safety by interfering with the operation of another electronically sensitive medical ... Class II Reported ongoing Distribution: Worldwide - United States Nationwide distribution including in the states of AK, AL, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ... [Official source for Brand Name: Branding is not applied to this product. Product Name: DVI display cables Model/Catal...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0169-2026%22) Nov 25, 2024 FDA device enforcement ### [Xhibit Telemetry Receiver, Model 96280, with Service Manual. Intended to provide monitoring system with patient data.](https://isitonrecall.com/recall/fda-device-z-0809-2025-xhibit-telemetry-receiver-model-96280-with-service-manual-intended-to-provide-monitoring-system-with/) Telemetry receiver systems may experience a Windows proxy Issue causing the system to shut down and restart (Offline displayed), lasting approximately 1 to 1.5 minutes, which will cause temporary loss of monitoring. If a clinical event occurred during this ... Class II Reported ongoing Distribution: US: OK, MN, IA, SC, NE, MI, NY, KY, GA, MO, MT, LA, WA, SD, CO, PA, WY, TX, ID, NJ, FL, OH, MS, OR, AK, IL, AR, KS, AL, TN, WI, VA, NM, CA, IN, RI, NV, MA, NC, ME, CT, AZ, MD, P... [Official source for Xhibit Telemetry Receiver, Model 96280, with Service Manual. Intended to provide monitoring syste...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0809-2025%22) Nov 25, 2024 FDA device enforcement ### [Xhibit Telemetry Receiver with Software, Model 96280. Intended to provide monitoring system with patient data.](https://isitonrecall.com/recall/fda-device-z-0810-2025-xhibit-telemetry-receiver-with-software-model-96280-intended-to-provide-monitoring-system-with-patie/) Telemetry receivers with affected software versions may experience unsolicited system shut down and restart (Offline displayed), lasting approximately 1 to 1.5 minutes, which will cause temporary loss of monitoring. If a clinical event occurred during this ... Class II Reported ongoing Distribution: US: MN, TX, TN, SC, OK, NM, GA, PA, OH, IA, AL, CO, AR, FL, MO, ME, LA, IL, WA, MA, WI, OR, MS, ID, NY, KS, PR. OUS: Canada, Taiwan, Czech Republic, France, Greece, Italy, Kuwai... [Official source for Xhibit Telemetry Receiver with Software, Model 96280. Intended to provide monitoring system with ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0810-2025%22) Apr 12, 2023 FDA device enforcement ### [Ultraview SL (UVSL) Command Module, Model 91496](https://isitonrecall.com/recall/fda-device-z-1503-2023-ultraview-sl-uvsl-command-module-model-91496/) Command modules will display the following when parameter processing is suspended, depending on software version: 1) Older versions will have waveforms present with no alarms, 2) Newer versions have waveforms absent with no alarms. This may cause clinicians... Class II Reported ongoing Distribution: US Nationwide distribution in the states of SD, KY, MO, WA, OH, NC, CA, OR, TX, GA, IL, OK, SC, PA, AL, KS, FL, ID, MI, MN, IA, NJ, MD, VA, AR, CT, NE, LA, AK, MS, ME, WV, NY, A... [Official source for Ultraview SL (UVSL) Command Module, Model 91496](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1503-2023%22) May 31, 2022 FDA device enforcement ### [Xhibit Telemetry Receiver, Model: 96280](https://isitonrecall.com/recall/fda-device-z-1513-2022-xhibit-telemetry-receiver-model-96280/) Software related alarm escalation defect occurs after approximately 25 days of continuous use. Technical alarm escalation for the following alarms, signal loss, all leads off, low battery, SpO2 sensor off, and signal interference, does not occur in the tele... Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide distribution in the states of NY, AR, CO, FL, NJ, AL, KY, TN, SC, WA, OK, MN, PA, GA, VA, CA, OH, IA, KS, MI, IN, TX, MT, MO, ME, LA, IL, ... [Official source for Xhibit Telemetry Receiver, Model: 96280](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1513-2022%22) ## Reasons in these listed records - Due to off-the-shelf display port component that has audio/video failures - Due to a manufacturing issue (i.e. malfunctioning of electrical Leakage tester). - Multi-parameter command module has a circuit board issue and when in Auto mode, Cardiac Output (CO) measurement may activate early, resulting in Bad Curve error with no CO measurement or Irregular Curve error with CO measurement not automatically excluded, which may result in ... - Due to display cables used for monitors were not in compliance with electromagnetic interference from inadequately shielded cables which may pose serious risk to patient's safety by interfering with the operation of another electronically sensitive medical device are in use. These examples come from this result page and are not a ranking of every recall reason. ## Checking Spacelabs Healthcare, Inc. ### Is there a recall on spacelabs healthcare, inc. right now? This archive contains 10 records, including 10 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Spacelabs Healthcare, Inc.](https://isitonrecall.com/check/?q=Spacelabs%20Healthcare%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)