Drug recall

Brand Name: Branding is not applied to this product. Product Name: DVI display cables Model/Catalog Number…

FDA recall event 97616 · Class II · Spacelabs Healthcare, Inc.

Key facts

Event ID 97616
Recall numbers Z-0167-2026, Z-0168-2026, Z-0169-2026
Recalling firm Spacelabs Healthcare, Inc.
Product type Devices
Products 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 to DVI-I male/male…, 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 to DVI-I male/male…, 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…
Classification Class II
Status Ongoing
Voluntary or mandated Firm Initiated
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…
Initiation date Sep 5, 2025
Report date Oct 22, 2025
City Snoqualmie
State WA
Country United States
FEI number 3010157426

At a glance

  • 1–9 Products in this recall
  • 10–99 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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