Verathon, Inc. recalls
Every recall we track for Verathon, Inc. — 6 in all, from 2019–2024 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
6 recalls since 2017.
All FDA recall records for Verathon, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 1 | 0 | 1 |
| 2020 | 0 | 1 | 1 | 0 | 2 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 2 | 0 | 2 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Verathon, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Verathon, Inc. recalls
5 shown- Lower riskMedical device
Verathon, Inc. recalls Brand Name: GlideScope Core 15-inch FHD Model/Catalog Number: 0570-0437 Software Version: Core 15 FHD v1.7 and earlier
Verathon recalls GlideScope Core 15-inch FHD monitors with software v1.7 and earlier due to potential image loss or degradation when connected to other devices. Affected units may require software updates to prevent issues.
VerathonApr 29, 2024 - Lower riskMedical device
Verathon, Inc. recalls GlideScope Go Monitors
Verathon recalls GlideScope Go Monitors with specific serial numbers and software versions for potential fluid ingress due to failed IP67 rating, which could cause loss of functionality.
VerathonJul 1, 2021 - Lower riskMedical device
Verathon, Inc. recalls BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be used for measuring the urine volume in the
Verathon recalls BladderScan Prime Plus Probe REF 0570-0395 due to handle cracking risk. Affected units have specific serial numbers listed. Stop using if handle cracks.
VerathonSep 29, 2020 - Use cautionMedical device
Verathon, Inc. recalls GlideScope Core OneTouch Smart Cable, REF: 0800 0601, an accessory to the GlideScope Video Laryngoscope System Per
Verathon recalls GlideScope Core OneTouch Smart Cable (REF 0800 0601) due to potential video disruption during intubation, risking critical patient delays. Affected users should check serial numbers and contact Verathon for details.
VerathonJun 5, 2020 - Lower riskMedical device
Verathon, Inc. recalls GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03
Verathon recalls GlideScope Video Laryngoscope manual with incorrect low-level disinfection instructions for titanium blades. Affected units include specific revisions and serial numbers. Contact for correction.
VerathonMar 31, 2019
Verathon, Inc. recall questions
How many recalls has Verathon, Inc. had?
6 recalls from Verathon, Inc. are on record with U.S. safety agencies, from 2019–2024.
What is the most recent Verathon, Inc. recall?
Verathon, Inc. recalls Brand Name: GlideScope Core 15-inch FHD Model/Catalog Number: 0570-0437 Software Version: Core 15 FHD v1.7 and earlier, dated Apr 29, 2024. Every Verathon, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Verathon, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Verathon, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.