software issue that causes an error screen on a portable vital signs monitor when attaching video Laryngoscope.
Reason for recall: software issue that causes an error screen on a portable vital signs monitor when attaching video Laryngoscope. Distribution: Worldwide - US Nationwide distribution including in the states of AL, AZ, CA, CO, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, TN, TX, UT, VA, WA, WI, WV, WY and the countries of AE, AF, AT, AU, BE, BO, CA, CH, CZ, DE, DK, ES, FI, FR, GB, HK, IE, IL, IS, IT, KY, MY, NL, NO, OM, PL, PT, RO, SA, SE, SG, SI, SL, TH, ZA. Quantity: 6,961 units Lot/code info: All Lots/ UDI-DI(s): 00-1004-R - 05060472440020 & 05060472442901; 00-1007-R - 05060472440013 & 05060472442918; 00-1024-R - 05060472441027 & 05060472442925; 00-1026-R - 05060472441058 & 05060472442932; 00-1004 - 05060472440624; 00-1007 - 05060472440655
05060472440020, 05060472442901, 05060472440013, 05060472442918, 05060472441027, 05060472442925, 05060472441058, 05060472442932, 05060472440624, 05060472440655
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.