GlideScope Go Video Monitors Recalled for Waterproof Rating Defect
Verathon recalls GlideScope Go Monitors due to failure to meet IP67 waterproof rating, which may allow fluid ingress and loss of functionality.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: FDA Class III device recall with no reported illnesses or injuries. The hazard is functional defect due to failure to meet waterproof specifications, not an acute safety threat. Per the rubric, FDA Class III recalls are typically scored 1 or 2.
Plain-English summary
Verathon, Inc. is recalling GlideScope Go Monitors (8,569 units) due to a waterproof rating defect in these handheld video monitors.
The recalled monitors failed to meet their labeled IP67 waterproof rating, which is designed to prevent fluid ingress. This defect may allow water or other fluids to enter the device, resulting in loss of functionality.
The affected monitors were distributed in the United States, Puerto Rico, and internationally across numerous countries. Specific affected serial numbers are identified in the recall notice.
Users of affected monitors should immediately discontinue use of recalled units and contact Verathon, Inc. for instructions regarding device replacement, repair, or return.
The recalled product
- Product
- GlideScope Go Monitors
- Manufacturer
- Verathon, Inc.
- Category
- Medical Device — Video Monitor
- Affected units
- 8,569
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- HM171547
- HM171548
- HM171550
- HM171622
- HM171627
- HM171629
- HM171630
- HM171631
- HM171632
- HM171633
- HM171634
- HM171635
- HM171636
- HM171637
- HM171638
- HM171639
- HM171642
- HM171643
- HM171644
- HM171645
Distribution
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