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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 94547

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
April 29, 2024
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Verathon, Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

2 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 2

Brand Name: GlideScope Core 15-inch Monitor Model/Catalog Number: 0570-0404 Product Description: Serialized Monitor

Z-2021-2024
Recall number
Z-2021-2024
Initiated
April 29, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Verathon, Inc.
Quantity
2568 devices

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Due to software issues, their is the potential for loss of image or a degradation of the image when using the monitor with other connectable devices.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software Manufacturing/Software Deployment

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Due to software issues, their is the potential for loss of image or a degradation of the image when using the monitor with other connectable devices.

Code information

Software Version: v1.9 and earlier/ UDI: UDI/DI: 00879123006639

Distribution pattern

US: AK AL AR AZ CA CO CT DC FL GA HI IA ID IL IN KS KY LA MA MD ME MI MN MO MS MT NC ND NE NH NJ NM NV NY OH OK ON OR PA QLD RI SC SD TN TX UT VA VIC WA WI WV WY OUS: Hong Kong, Indonesia, Saudi Arabia

device · product 2 of 2

Brand Name: GlideScope Core 15-inch FHD Model/Catalog Number: 0570-0437 Software Version: Core 15 FHD v1.7 and earlier Product Description: Serialized Monitor

Z-2022-2024
Recall number
Z-2022-2024
Initiated
April 29, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Verathon, Inc.
Quantity
1706 devices

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Due to software issues, their is the potential for loss of image or a degradation of the image when using the monitor with other connectable devices.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software Manufacturing/Software Deployment

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Due to software issues, their is the potential for loss of image or a degradation of the image when using the monitor with other connectable devices.

Code information

Software versions: v1.7 and earlier/UDI/DI: 00879123008596

Distribution pattern

US: AK AL AR AZ CA CO CT DC FL GA HI IA ID IL IN KS KY LA MA MD ME MI MN MO MS MT NC ND NE NH NJ NM NV NY OH OK ON OR PA QLD RI SC SD TN TX UT VA VIC WA WI WV WY OUS: Hong Kong, Indonesia, Saudi Arabia