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Use caution Medical device recall · FDA · Published September 5, 2025

Spacelabs DVI Display Cables: Risk of Medical Device Interference

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.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-0169-2026Medical deviceSpacelabs Healthcare ›
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Contact the company

Recalling firmSpacelabs Healthcare, Inc.35301 Se Center St · Snoqualmie, WA 98065-9216
✎ GovInfoNow plain-language explainer

Spacelabs Healthcare is recalling DVI display cables that could interfere with medical devices, potentially causing patient safety risks. This recall affects cables sold with specific medical monitors. Read more at govinfonow.com/recall/51426-spacelabs-dvi-display-cables-risk-of-medical-device-interference.

Source Summary by GovInfoNow · govinfonow.com/recall/51426-spacelabs-dvi-display-cables-risk-of-medical-device-interference · Updated August 18, 2026 · FDA enforcement record: FDA #Z-0169-2026

Cite this page

“Spacelabs DVI Display Cables: Risk of Medical Device Interference.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/51426-spacelabs-dvi-display-cables-risk-of-medical-device-interference. Based on FDA recall #Z-0169-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0169-2026%22&limit=1).

The FDA announced on Sept. 5, 2025, that Spacelabs Healthcare is recalling DVI display cables due to inadequate shielding that may interfere with other medical devices. The agency issued recall number Z-0169-2026 for the voluntary Class II action.

How to tell if you have it

  • Brand: Spacelabs Healthcare
  • Product Name: DVI display cables
  • Model/Catalog Number: 012-0893-01
  • UPC: 10841522131455
  • UPC: 10841522131479

The hazard

The cables were not in compliance with electromagnetic interference standards due to inadequate shielding. This failure may pose a serious risk to patient safety by interfering with the operation of another electronically sensitive medical device.

Context

GovInfoNow's records show Spacelabs Healthcare has 10 other recalls on record since Jan. 17, 2018. Other recent recalls of similar products include Spacelabs Xhibit Central Station Model 96102 (June 4, 2026), Spacelabs Ultraview SL Command Module Software Recall (March 26, 2026), and Spacelabs Healthcare Multi-parameter Command Module Model 91496 Recall (Feb. 27, 2026). Other recent recalls of similar products include Canon Vantage Galan 3T Medical Device Recall (Oct. 16, 2025), GE Allia Moveo X-ray System Recall (April 20, 2026), and Philips IntelliVue MP70 Monitor Recall (Oct. 31, 2025).

How to tell if you have this one

Check for model number 012-0893-01 on the cable. These cables were sold with Spacelabs 91390 or 91393 monitors.

  • Brand
    Spacelabs Healthcare
  • Product
    Brand Name: Branding is not applied to this product. Product Name: DVI display cables Model/Catalog Number: 012-0893-01
  • Category
    Medical device
FDA recall event · 3 products

All 3 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    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, NE, NH, NJ, NM, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, VA, WA, WI, WY and the countries of AFG, ARE, ARG, AUS, AUT, BGD, BHR, BOL, BRA, BRN, CAN, CHE, CHL, CHN, COL, CRI, CYP, CZE, DOM, DZA, ECU, EGY, ESP, FRA, GBR, GRC, GTM, GUM, HKG, IDN, IND, IRL, IRN, ISR, ITA, JOR, KWT, LBN, MAR, MEX, MYS, NLD, NZL, OMN, PAK, PAN, PER, PHL, PLS, POL, PRI, PRT, PRY, QAT, ROM, SAU, SGP, SLV, SRB, THA, TTO, TUN, TUR, TWN, VNM.
Recall numberProduct, codes & lotsQuantity
Z-0167-2026Brand 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 to DVI-I male/male display cable. Component: Yes, the cable is an external display cable used with the 91390 and 91393; Lot Code: UDI-DI for products that are used with the display cables. (01)10841522131479 (Xprezzon), (01)10841522131455 (Qube)8179
Z-0168-2026Brand 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 to DVI-I male/male display cable. Component: Yes, the cable is an external display cable used with the 91390 and 91393; Lot Code: UDI-DI for products that are used with the display cables. (01)10841522131479 (Xprezzon), (01)10841522131455 (Qube)820
Z-0169-2026Brand 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 to DVI-I male/male display cable. Component: Yes, the cable is an external display cable used with the 91390 and 91393; Lot Code: UDI-DI for products that are used with the display cables. (01)10841522131479 (Xprezzon), (01)10841522131455 (Qube)16898
Based on the official FDA remedy

What to do — step by step

  1. Check Cable Model

    Look for model number 012-0893-01 on the DVI display cable.

  2. Replace Cable

    Replace the cable with a model that meets electromagnetic shielding standards.

Where it went and when

Where it was distributed

Distributed nationwide and abroad; the notice names 43 states.

Alaska: named in the noticeAKMaine: named in the noticeMEVermont: nationwideVTNew Hampshire: named in the noticeNHWashington: named in the noticeWAIdaho: named in the noticeIDMontana: named in the noticeMTNorth Dakota: nationwideNDMinnesota: named in the noticeMNIllinois: named in the noticeILWisconsin: named in the noticeWIMichigan: named in the noticeMINew York: named in the noticeNYRhode Island: named in the noticeRIMassachusetts: named in the noticeMAOregon: named in the noticeORNevada: nationwideNVWyoming: named in the noticeWYSouth Dakota: named in the noticeSDIowa: named in the noticeIAIndiana: named in the noticeINOhio: named in the noticeOHPennsylvania: named in the noticePANew Jersey: named in the noticeNJConnecticut: named in the noticeCTCalifornia: named in the noticeCAUtah: nationwideUTColorado: named in the noticeCONebraska: named in the noticeNEMissouri: named in the noticeMOKentucky: named in the noticeKYWest Virginia: nationwideWVVirginia: named in the noticeVAMaryland: named in the noticeMDDelaware: named in the noticeDEArizona: named in the noticeAZNew Mexico: named in the noticeNMKansas: named in the noticeKSArkansas: nationwideARTennessee: named in the noticeTNNorth Carolina: named in the noticeNCSouth Carolina: named in the noticeSCDistrict of Columbia: nationwideDCOklahoma: named in the noticeOKLouisiana: named in the noticeLAMississippi: named in the noticeMSAlabama: named in the noticeALGeorgia: named in the noticeGAHawaii: nationwideHITexas: named in the noticeTXFlorida: named in the noticeFLPuerto Rico: named in the noticePR

FDA 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, NE, NH, NJ, NM, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX,…” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: Alabama, Alaska, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, New Hampshire, New Jersey, New Mexico, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Virginia, Washington, Wisconsin, Wyoming.

Recall timeline

FDA published this recall 47 days after the firm started it.

1. Firm started the recall: Sep 5, 202512. FDA classified it Class II: Oct 16, 202523. Published in FDA’s Enforcement Report: Oct 22, 202532025
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

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-0169-2026 (September 5, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0169-2026 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 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