Data Foundry

Medical device recalls 2021

GlideScope Go Monitors — Class III medical device recall Z-2172-2021

Ongoing recall by Verathon, Inc., reported 2021-08-11, distributed in AK, AL, AR, AZ, CA, CO, CT, DC…. Handheld video monitor failed to meet the labeled IP67 rating which may allow fluid ingress into the monitor r

Recall numberZ-2172-2021
Product typeMedical device
ClassificationClass III
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmVerathon, Inc., Bothell, WA, United States
Recall initiated2021-07-01
Classified2021-07-30
Reported by FDA2021-08-11
DistributedAK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, GU, 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, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY
Countries outside the USAU, CA, CH, CZ, DE, DK, EE, ES, FR, GB, GR, HK, IE, IL, IS, IT, KR, KW, LU, MY, NL, NZ, OM, PH, PT, QA, RO, SA, SE, SG, TH, TW, ZA
Quantity8,569
Reason classeslabeling
Serial numbers1450070, HM082506, HM171547, HM171548, HM171550, HM171622, HM171627, HM171629, HM171630, HM171631, HM171632, HM171633, HM171634, HM171635, HM171636, HM171637, HM171638, HM171639, HM171642, HM171643, HM171644, HM171645, HM171653, HM171654, HM171655 and 475 more
Model numbers0570-0366

Product

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2172-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.