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AC-powered adjustable medical beds with built-in electric DC actuators and controls.

FDA Device Recall #Z-1136-2022 — Class II — April 11, 2022

Recall Summary

Recall Number Z-1136-2022
Classification Class II — Moderate risk
Date Initiated April 11, 2022
Status Terminated
Voluntary Voluntary: Firm initiated

Recalling Firm

Firm Umano Medical, Inc.
Location L'Islet
Product Type Devices
Quantity 355 units

Product Description

AC-powered adjustable medical beds with built-in electric DC actuators and controls.

Reason for Recall

There is a potential hazard of uninterrupted motion of the Motorized Wheel System due to the possible failure of a component in the electrical system of the Product.

Distribution Pattern

Worldwide distribution - US Nationwide distribution in the states of CA, PA, AL, GA, AZ, MN, FL, WA, OK, NY, ND, AR, MO, NC, UT, TX, WI, and the countries of Australia, Ireland, and Canada.

Lot / Code Information

Model number: 200-0000; UDI: 00670482000487; Serial Numbers: 20004934, 20004933, 20004932, 20004931, 20004930, 20004929, 20004928, 20004927, 20004926, 20004925, 20004924, 20004923, 20004914, 20004886, 20004885, 20004884, 20004883, 20004882, 20004881, 20004880, 20004879, 20004878, 20004877, 20004876, 20004875, 20004874, 20004873, 20004872, 20004871, 20004870, 20004869, 20004868, 20004867, 20004866, 20004865, 20004864, 20004863, 20004862, 20004861, 20004860, 20004859, 20004858, 20004857, 20004856, 20004855, 20004854, 20004853, 20004852, 20004851, 20004850, 20004849, 20004848, 20004847, 20004846, 20004845, 20004844, 20004843, 20004842, 20004841, 20004840, 20004839, 20004812, 20004811, 20004810, 20004809, 20004808, 20004807, 20004806, 20004805, 20004804, 20004803, 20004802, 20004801, 20004800, 20004799, 20004798, 20004797, 20004796, 20004795, 20004794, 20004793, 20004792, 20004791, 20004790, 20004789, 20004788, 20004787, 20004786, 20004785, 20004784, 20004783, 20004782, 20004781, 20004712, 20004711, 20004710, 20004709, 20004777, 20004772, 20004721, 20004720, 20004719, 20004718, 20004717, 20004662, 20004661, 20004660, 20004659, 20004658, 20004657, 20004656, 20004655, 20004654, 20004653, 20004652, 20004651, 20004708, 20004707, 20004706, 20004705, 20004704, 20004703, 20004702, 20004701, 20004700, 20004699, 20004698, 20004697, 20004696, 20004695, 20004694, 20004693, 20004692, 20004691, 20004690, 20004689, 20004688, 20004687, 20004686, 20004685, 20004684, 20004683, 20004682, 20004681, 20004680, 20004679, 20004678, 20004677, 20004676, 20004675, 20004674, 20004673, 20004650, 20004649, 20004648, 20004647, 20004646, 20004645, 20004644, 20004643, 20004642, 20004641, 20004640, 20004639, 20004638, 20004637, 20004636, 20004627, 20004626, 20004625, 20004624, 20004623, 20004622, 20004621, 20004620, 20004619, 20004618, 20004617, 20004616, 20004615, 20004614, 20004613, 20004612, 20004611, 20004610, 20004609, 20004608, 20004607, 20004606, 20004605, 20004542, 20004541, 20004540, 20004539, 20004538, 20004537, 20004536, 20004535, 20004534, 20004533, 20004532, 20004531, 20004530, 20004529, 20004528, 20004527, 20004526, 20004525, 20004524, 20004523, 20004522, 20004521, 20004520, 20004519, 20004518, 20004517, 20004516, 20004515, 20004514, 20004513, 20004512, 20004511, 20004510, 20004509, 20004508, 20004507, 20004506, 20004505, 20004504, 20004503, 20004502, 20004501, 20004500, 20004499, 20004498, 20004497, 20004496, 20004495, 20004494, 20004493, 20004492, 20004491, 20004490, 20004489, 20004488, 20004487, 20004486, 20004485, 20004484, 20004483, 20004482, 20004481, 20004480, 20004479, 20004478, 20004477, 20004476, 20004475, 20004474, 20004473, 20004466, 20004465, 20004464, 20004463, 20004462, 20004461, 20004460, 20004459, 20004458, 20004457, 20004456, 20004455, 20004454, 20004453, 20004452, 20004451, 20004450, 20004449, 20004448, 20004447, 20004446, 20004445, 20004444, 20004443, 20004442, 20004441, 20004440, 20004439, 20004438, 20004437, 20004417, 20004416, 20004415, 20004414, 20004413, 20004412, 20004374, 20004373, 20004372, 20004371, 20004370, 20004369, 20004368, 20004367, 20004366, 20004247, 20004246, 20004380, 20004220, 20004219, 20004218, 20004210, 20004209, 20004208, 20004207, 20004206, 20004205, 20004204, 20004203, 20004202, 20004035, 20004034, 20004033, 20004032, 20004031, 20004030, 20004029, 20004028, 20004027, 20004022, 20004023, 20004024, 20004025, 20004026, 20004238, 20004239, 20004240, 20004241, 20004242, 20004243, 20004244, 20004248, 20004249, 20004250, 20004251, 20004252, 20004332, 20004333, 20004375, 20004376, 20004377, 20004378, 20004379, 20004835, 20004245

Other Recalls from Umano Medical, Inc.

Recall # Classification Product Date
Z-1135-2022 Class II AC-powered adjustable medical beds with built-i... Apr 11, 2022
Z-2205-2020 Class II AC Powered hospital adjustable bed. May 4, 2020

Frequently Asked Questions

Contact your physician immediately if you use an electrical device or implant affected by this recall. For external devices (monitors, pumps), stop using the device and contact the manufacturer for a replacement. For implanted devices (pacemakers, ICDs), your cardiologist will assess whether you need device replacement surgery — the decision depends on how dependent you are on the device and the actual failure rate observed in the field. Do not attempt to repair or modify a recalled electrical medical device yourself. Monitor for any new or unusual symptoms and report them to your doctor.

Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency — Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.

Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.

What Should You Do?

Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.

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