GlideScope Go Monitors
Reported: August 11, 2021 Initiated: July 1, 2021 #Z-2172-2021
Product Description
GlideScope Go Monitors
Reason for Recall
Handheld video monitor failed to meet the labeled IP67 rating which may allow fluid ingress into the monitor resulting in loss of functionality.
Details
- Recalling Firm
- Verathon, Inc.
- Units Affected
- 8,569
- Distribution
- U.S.: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, Guam, 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, OR, PA, RI, Puerto Rico, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV and WY. O.U.S.: Australia, Brunei Darussalam, Canada, Czech Republic, Denmark, Estonia, Falkland Island (Malvinas), France, Germany, Greece, Hong Kong, Iceland, Ireland, Israel, Italy, Kuwait, Luxembourg, Malaysia, New Zealand, Oman, Papua New Guinea, Philippines, Portugal, Qatar, Reunion, Romania, Saudi Arabia, Singapore, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, The Netherlands, United Arab Emerita, and United Kingdom.
- Location
- Bothell, WA
Frequently Asked Questions
What product was recalled? ▼
GlideScope Go Monitors. Recalled by Verathon, Inc.. Units affected: 8,569.
Why was this product recalled? ▼
Handheld video monitor failed to meet the labeled IP67 rating which may allow fluid ingress into the monitor resulting in loss of functionality.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 11, 2021. Severity: Low. Recall number: Z-2172-2021.
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