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FDA (Device enforcement)Recalled 2025-02-05class i

Baxter Healthcare Corporation: Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009

Hazard

There is the potential for missing motor mounting screws, which may have occurred during the servicing process.

Details from the source

Reason for recall: There is the potential for missing motor mounting screws, which may have occurred during the servicing process. Distribution: US: Nationwide Quantity: 323 units Lot/code info: UDI/DI 00085412610900, Serial Numbers: 3020290, 3020992, 3020996, 3021929, 3023080, 3023183, 3023537, 3023758, 3500529, 3502799, 3502864, 3510806, 3511639, 3512647, 3514801, 3516888, 3517399, 3517517, 3518558, 3519053, 3564064, 3564818, 3565462, 3565620, 3566022, 3566254, 3567145, 3567218, 3567998, 3568527, 3568922, 3570910, 3571100, 3571598, 3571972, 3573147, 3573504, 3574293, 3575033, 3575107, 3576026, 3576443, 3656732, 3657316, 3657541, 3657814, 3657821, 3657995, 3659259, 3660176, 3660244, 3662986, 3664495, 3665624, 3721608, 3721910, 3721946, 3722620, 3723725, 3724211, 3730270, 3730408, 3732309, 3732476, 3734858, 3735010, 3735261, 3735734, 3738122, 3744219, 3744455, 3746159, 3746749, 3749111, 3749929, 3764591, 3767418, 3519969, 3520138, 3520706, 3520746, 3520829, 3521120, 3521338, 3606099, 3607097, 3607681, 3608730, 3609223, 3610668, 3610820, 3611120, 3611140, 3611650, 3612298, 3612886, 3613052, 3614035, 3615599, 3615816, 3616449, 3666443, 3666451, 3667116, 3668076, 3668654, 3668851, 3669058, 3669126, 3669307, 3670942, 3671444, 3672061, 3672846, 3676099, 3677241, 3679511, 3680542, 3681596, 3681981, 3686743, 3689421, 3691453, 3691496, 3693341, 3696268, 3618354, 3619039, 3619876, 3620296, 3620427, 3620631, 3620643, 3620757, 3621068, 3621252, 3621777, 3623915, 3623963, 3624131, 3624546, 3627519, 3628177, 3630964, 3632085, 3632710, 3632830, 3633267, 3634729, 3634792, 3699321, 3699388, 3699822, 3699917, 3700350, 3700551, 3701785, 3703127, 3703425, 3703513, 3703840, 3704056, 370

UPC codes

00085412610900

Source

Official record: FDA (Device enforcement)

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

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