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FDA (Device enforcement)Recalled 2026-06-10class ii

ICU Medical, Inc.: ICU Medical Plum Solo Precision IV Pump, v1.0.3, Item Number 400010401; infusion pump

Hazard

In a specific scenario, the pump will not decrement the Volume to be Infused (VTBI) displayed on the Delivery screen and may deliver up to twice the VTBI at the programmed rate.

Details from the source

Reason for recall: In a specific scenario, the pump will not decrement the Volume to be Infused (VTBI) displayed on the Delivery screen and may deliver up to twice the VTBI at the programmed rate. Distribution: Worldwide distribution - US Nationwide and the country of Canada. Quantity: 5059 units Lot/code info: UDI/DI +M335400011, Serial Numbers: 60000316, 60000363, 60000375, 60000388, 60000428, 60000451, 60000469, 60000495, 60000529, 60000569, 60000580, 60000637, 60000643, 60000647, 60000652, 60000668, 60000670, 60000689, 60000692, 60000695, 60000703, 60000706, 60000710, 60000712, 60000716, 60000718, 60000724, 60000726, 60000754, 60000757, 60000759, 60000765, 60000775, 60000776, 60000781, 60000790, 60000793, 60000801, 60000805, 60000816, 60000830, 60000835, 60000850, 60000857, 60000860, 60000879, 60000883, 60000886, 60000899, 60000903, 60000909, 60000916, 60000917, 60000920, 60000927, 60000933, 60000938, 60000939, 60000942, 60000944, 60000948, 60000951, 60000954, 60000959, 60000960, 60000964, 60000966, 60000967, 60000980, 60000985, 60000987, 60000988, 60000990, 60001007, 60001008, 60001013, 60001028, 60001030, 60001031, 60001034, 60001035, 60001036, 60001037, 60001038, 60001039, 60001040, 60001041, 60001042, 60001043, 60001044, 60001045, 60001047, 60001048, 60001049, 60001050, 60001051, 60001052, 60001053, 60001054, 60001055, 60001056, 60001057, 60001058, 60001060, 60001061, 60001062, 60001063, 60001064, 60001065, 60001066, 60001067, 60001068, 60001069, 60001070, 60001071, 60001072, 60001073, 60001074, 60001075, 60001076, 60001077, 60001078, 60001079, 60001080, 60001081, 60001082, 60001083, 60001084, 60001085, 60001086, 60001087, 60001088, 60001089, 60001090, 60001091, 60001092, 60001093, 60001094, 60001095, 60001096, 60001097, 60001098, 60001099, 60001100, 60001101, 60001102, 6000

Source

Official record: FDA (Device enforcement)

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

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