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FDA (Device enforcement)Recalled 2025-04-16class ii

Remote Diagnostic Technologies Ltd.: Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP, without headset dock), 00-1007-R and 00-1007 (Tempus Pro non-printer, IBP, with headset d

Hazard

software issue that causes an error screen on a portable vital signs monitor when attaching video Laryngoscope.

Details from the source

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

UPC codes

05060472440020, 05060472442901, 05060472440013, 05060472442918, 05060472441027, 05060472442925, 05060472441058, 05060472442932, 05060472440624, 05060472440655

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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