# FDA recall Z-0168-2026

> **Spacelabs Healthcare, Inc.** · Class II · device recall initiated 2025-09-05.

## Product

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 to DVI-I male/male display cable.  Component: Yes, the cable is an external display cable used with the 91390 and 91393

## Reason for recall

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.

## 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.

## Key facts

- **Recall number:** Z-0168-2026
- **Recalling firm:** Spacelabs Healthcare, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-09-05
- **Report date:** 2025-10-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Snoqualmie, WA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0168-2026

## Citation

> AI Analytics. FDA recall Z-0168-2026. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-0168-2026. Source: US FDA. Licensed CC0.

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