Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0168-2026 — 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

U.S. FDA — Device Enforcement · United States · 2025-09-05 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0168-2026
Date of alert
2025-09-05
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Spacelabs Healthcare, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10841522131479
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.