Verathon, Inc.
Complete recall history across all FDA and CPSC categories — 13 total recalls
Verathon, Inc. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Device Recalls (13)
FDA medical device enforcement actions by Verathon, Inc.
| Date | Product | Reason | Class |
|---|---|---|---|
| Apr 29, 2024 | Brand Name: GlideScope Core 15-inch Monitor Model/Catalog Number: 0570-0404 ... | Due to software issues, their is the potential for loss of image or a degrada... | Class II |
| Apr 29, 2024 | Brand Name: GlideScope Core 15-inch FHD Model/Catalog Number: 0570-0437 Sof... | Due to software issues, their is the potential for loss of image or a degrada... | Class II |
| Jul 1, 2021 | GlideScope Go Monitors | Handheld video monitor failed to meet the labeled IP67 rating which may allow... | Class III |
| Sep 29, 2020 | BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be us... | Due to a change in handle material and process, probe handle may crack. | Class II |
| Jun 5, 2020 | GlideScope Core OneTouch Smart Cable, REF: 0800 0601, an accessory to the Gli... | When video laryngoscopy system users apply, twisting motions while connecting... | Class I |
| Mar 31, 2019 | GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03 | A typographical error in the Operations & Maintenance Manual incorrectly iden... | Class II |
| Jan 29, 2016 | GlideScope Titanium Single-Use Video Laryngoscope. It is a single-use video l... | The firm has become aware of the potential for disruption (flickering) in the... | Class I |
| Nov 30, 2015 | GlideScope Video Laryngoscope (GVL), Part Number GVL 3 - 0574-0007; GVL 4 - 0... | Certain models and serial numbers of GlideScope GVL and AVL laryngoscope blad... | Class II |
| Nov 30, 2015 | BladderScan BVI 9600, Model Numbers: 0270-0451, 0270-0452, 0270-0754, and U27... | The firm is providing customers with an updated Operations and Maintenance Ma... | Class II |
| Nov 30, 2015 | GlideScope AVL Video Laryngoscope (AVL), Part Number AVL 3- 0574-0115; AVL 4-... | Certain models and serial numbers of GlideScope GVL and AVL laryngoscope blad... | Class II |
| Apr 13, 2015 | GlideScope Video Laryngoscope Reusable Blades (GVL 3, 4, 5 and AVL 2, 3, 4, 5... | Verathon has revised the Operations and Maintenance Manual (OMM) to specifica... | Class II |
| May 8, 2013 | GlideScope Video Laryngoscope (GVL) 3, 4, 5 and GlideScope (AVL) 2, 3, 4 and... | Verathon GlideScope Reusable GVL and AVL Blades are being recalled due to the... | Class I |
| Oct 25, 2012 | The GlideScope Video Laryngoscope (GVL) is a video laryngoscope that incorpor... | Re-usable video laryngoscope blades of the GlideScope GVL3, GVL4, and GVL5 we... | Class I |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
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