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Use caution Medical device recall · FDA · Published January 17, 2018

Spacelabs Healthcare Xhibit Telemetry Receiver Model 96280: Telemetry Beds Dropping Off

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.

🇺🇸 FDA recall #Z-0532-2018Medical deviceSpacelabs Healthcare ›
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Contact the company

Recalling firmSpacelabs Healthcare Inc35301 SE Center St · Snoqualmie, WA 98065-9216
✎ GovInfoNow plain-language explainer

Spacelabs Healthcare is recalling specific model 96280 telemetry receivers with software version 1.1 because they can drop off the central station, leading to loss of patient monitoring. This poses a risk of missing critical patient data during medical procedures. Read more at govinfonow.com/recall/72131-spacelabs-healthcare-xhibit-telemetry-receiver-model-96280-telemetry-beds-dropping.

Source Summary by GovInfoNow · govinfonow.com/recall/72131-spacelabs-healthcare-xhibit-telemetry-receiver-model-96280-telemetry-beds-dropping · Updated August 31, 2026 · FDA enforcement record: FDA #Z-0532-2018

Cite this page

“Spacelabs Healthcare Xhibit Telemetry Receiver Model 96280: Telemetry Beds Dropping Off.” GovInfoNow, updated August 31, 2026. https://govinfonow.com/recall/72131-spacelabs-healthcare-xhibit-telemetry-receiver-model-96280-telemetry-beds-dropping. Based on FDA recall #Z-0532-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0532-2018%22&limit=1).

The FDA announced on Jan. 17, 2018, that Spacelabs Healthcare Inc. is recalling its Xhibit Telemetry Receiver, Model 96280, due to telemetry beds dropping off the central station and causing a loss of monitoring. The agency issued recall number Z-0532-2018 for the voluntary Class II action.

How to tell if you have it

  • Brand: Spacelabs Healthcare
  • Product: Xhibit Telemetry Receiver, Model 96280, software version 1.1
  • Serial numbers: 6280-000359, 6280-000340, 6280-000336, 6280-000503, 6280-000502, 6280-000500, 6280-000496, 6280-000495, 6280-000327, 6280-000260, 6280-000566, 6280-000290
  • Quantity: 12 systems
  • Distribution: VA, NJ, MI, GA, and France

The hazard

Spacelabs has received multiple complaints reporting telemetry beds dropping off the Spacelabs Central Station resulting in a loss of monitoring.

Context

GovInfoNow's records show Spacelabs Healthcare, Inc. has 10 other recalls on record since Jan. 28, 2019. Other recent recalls of similar products include GE HealthCare Telemetry Server Recall (April 24, 2026) and GE HealthCare CARESCAPE Telemetry Server ARK-2250L Recall (April 24, 2026).

How to tell if you have this one

Check for the model number 96280 and software version 1.1 on the device. Serial numbers listed include 6280-000359, 6280-000340, and others.

  • Brand
    Spacelabs Healthcare
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Device Serial Number

    Look for the serial numbers listed in the recall notice: 6280-000359, 6280-000340, 6280-000336, 6280-000503, 6280-000502, 6280-000500, 6280-000496, 6280-000495, 6280-000327, 6280-000260, 6280-000566, 6280-000290.

Where it went and when

Where it was distributed

Distributed in 4 states, and outside the U.S.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: yesMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: yesNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: yesVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: yesGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “US Distribution to the states of : VA, NJ, MI, GA, and Internationally to France” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Georgia, Michigan, New Jersey, Virginia.

Recall timeline

FDA terminated this recall 10 months after the firm started it.

1. Firm started the recall: Jan 17, 201812. FDA classified it Class II: Feb 5, 201823. Published in FDA’s Enforcement Report: Feb 14, 201834. FDA terminated the recall: Nov 29, 201842018
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-0532-2018 (January 17, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0532-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on August 31, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA