Class I FDA device recall · Z-0776-2024

Class I — the FDA judged there is a reasonable probability that use of the product would cause serious harm or death.

This is the FDA's risk judgment for this recall. It describes the potential of the product as a category — it does not establish that any specific unit harmed anyone.

EvAir CPRSR Kit Upgrade: a) DISS/CEE 7/7 230V 50/60 HZ, Model Number M1230849; b) DISS/NEMA 5-15 115V 60 HZ, Model Number M1230847; c) NIST/BS 1363 230V 50/60 HZ, Model Number M1230849; d) NIST/BS 546 230V 50/60 HZ, Model Number M1230849; e) NIST/CEE 7/7 230V 50/60 HZ, Model Number M1230849;

Why it was recalled

GE HealthCare has become aware of elevated levels of formaldehyde when the EVair or EVair 03 (Jun-Air) optional compressors are used with the CARESCAPE R860 or Engstr¿m Carestation/Pro ventilators, respectively. These elevated results were observed in preliminary testing that was conducted at an elevated room temperature of 40oC (104oF), at the lowest possible flow condition of 2 L/min (worstcase, minimum bias flow with no additional ventilation), and all of the gas being supplied from the compressor (i.e., FiO2 of 21% / no supplemental oxygen). GE HealthCare is continuing to evaluate the root cause for these elevated levels of formaldehyde. While these test conditions are not representative of typical clinical use conditions,GE HealthCare is taking this action to further reduce the potential for patient exposure.

Is your unit affected?

The recall covers only the specific lots or serial numbers the FDA listed. Enter the lot or serial number from your product's label and we'll check it against that list.

A match means your unit may be covered — stop and call your pharmacist before doing anything. No match suggests it isn't covered, but confirm anyway: code formats vary and lists can be incomplete. Your unit not being listed does not guarantee it is safe, and being listed does not mean you have been harmed.

Show the FDA's listed lot / code information

a) DISS/CEE 7/7 230V 50/60 HZ, Model Number M1230849; UDI/DI *TBP* , Serial Numbers: GEB08691, GEB08778, GEB08726, GEB08791, GEB08782, GEB08780, GEB08651, GEB08694, GEB08776, GEA05881, GEA05877, GEA05883, GEA05882, GEA05880, GEA04101, GEA05302, GEA04586, GEA04621, GEA05372, GEA05304, GEA04587, GEA04556, GEA05369, GEA04588, GEA04620, GEA04098, GEA05303, GEA05301, GEA04618, GEA04619, GEA04099, GEA04589, GEA04100, GEB08768, GEA04550, GEA06057, GEA06119, GEA06116, GEA07318, GEA06709, GEA07513, GEA07155, GEA07162, GEA07434, GEA07428, GEA07433, GEA07511, GEA07431, GEA07568, GEA07528, GEA07152, GEA03205, GEA03202, GEA03204, GEA03203, GEA06055, GEA06117, GEA04802, GEA06118, GEA06056, GEA04553, GEA04800, GEA04803, GEA04801, GEA07822, GEA07842, GEA07840, GEA07839, GEA07851, GEA07804, GEA07901, GE021663, GE021666, GEA03006, GEA03008, GEA03007, GEA03005;    b) DISS/NEMA 5-15 115V 60 HZ, Model Number M1230847; UDI/DI *TBP* , Serial Numbers:  GEA07877, GEA07866, GEA08370, GEA08369, GEA07893, GEA07892, GEB08822, GEB08809, GEB08827, GEB08820, GEB08813, GEA06781, GEA06778, GEB08835, GEB08817, GEA07895, GEA07859, GEA07896, GEA07861, GEB08821;   c) NIST/BS 1363 230V 50/60 HZ, Model Number M1230849; UDI/DI *TBP* , Serial Numbers:  GEA06054, GEB08069, GEB07991, GEB07965, GEB08171, GEB08276, GEB07412, GEB07440, GEB03790, GEB08164, GEB07396, GEB08242, GEB08172, GEB08243, GEB08245, GEB08239, GE021229, GE021230, GEA04266, GEA04269, GEA04265, GEA04264, GEA04263, GEB09817, GEB09804, GEB09808, GEB09855, GEB09863, GEB09719, GEB09853, GEB09823, GEB09856, GEB09822, GEB08785, GEB08792, GEB08781;   d) NIST/BS 546 230V 50/60 HZ, Model Number M1230849; UDI/DI *TBP* , Serial Numbers:  GEB09437, GEB09803, GEB09824, GEB09819, GEB09402, GEB09391, GEA07666, GEA07643, GEA07663, GEA07857, GEA07914, GEB09401, GEB09932, GEA07904, GEA07902, GEA07610, GEA07856, GEA07652, GEA07711, GEA07720, GEA07665, GEA07609, GEA07634, GEA07599, GEA07577, GEA07611, GEA07633, GEA07655, GEA07845, GEA07617, GEA07607, GEB09319, GEB09827, GEB09829, GEB09821, GEB09825, GEB09828, GEB09801, GEB09806, GEB09398, GEB09452, GEB09952, GEB09947, GEA07625, GEA07710, GEA07830, GEA07792, GEA07382, GEA07829, GEA07445, GEA07658, GEA07442, GEA07653, GEA07713, GEA03057, GEA03058, GEA03059, GEA03247, GEA03246, GEA03029, GEA03032, GEA03030, GEA03060, GEA03031, GEB09453, GEB09811, GEA07834, GEB08137, GEA03520, GEA03522, GEA03518, GEB09440, GEB09436, GEB09861, GEB09837, GEB09849, GEB08155, GEB08162, GEB09314, GEA03870, GEA03871, GEA03872, GEA03873, GEA07903, GEA07571, GEA07809, GEB09499, GEB09447, GEB09491, GEB09418, GEB09500, GEB09431, GEB09371, GEB09376, GEB09339, GEB09393, GEB09334, GEB09779, GEB09854, GEB09782, GEB09831, GEB09830, GEB09948, GEB09917, GEB09847, GEB09945, GEA07656, GEA07787, GEA03558, GEA03544, GEA03535, GEA03532, GEA03557, GEA07618, GEA07826, GEA07426, GEA07444, GEA07812, GEA03527, GEA03529, GEA03521, GEA03528, GEB09422, GEB09427, GEB09430, GEA03559, GEA03533, GEA03534, GEA03501, GEA03500, GEA03502, GEA03503, GEA03530, GEA07608, GEA07591, GE020660, GE020657, GEA07576, GEA07578, GEA07569, GEB08738, GEB08737, GEB08702, GEB09317, GEB09318, GEB09394, GEB09451, GEB09407;     e) NIST/CEE 7/7 230V 50/60 HZ, Model Number M1230849; UDI/DI *TBP* , Serial Numbers:  GEB08741, GEB08755, GEB08690, GEB08704, GEB08697, GEB08744, GEB08747, GEB08722, GEB08648, GEB08709, GEB08669, GEB08896, GEB08905, GEB08729, GEB08902, GEB08903, GEB08899, GEB08897, GEB08898, GEB08893, GEB08901, GEB08908, GEB08907, GEB08793, GEB08798, GEB08789, GEB08895, GEB08742, GEB08894, GEB08788, GEB08644, GEB08761, GEB08685, GEB08787, GEB08770, GEB08667, GEB08665, GEB08757, GEB08765, GEB08777, GEB08687, GEB08666, GEB08784, GEB08745, GEB08753, GEB08713, GEB08752, GEB08711, GEB08695, GEB08717, GEB08700, GEB08714, GEB08774, GEB08775, GEB08710, GEB08763, GEB08649, GEB08689, GEB08758, GEB08764, GEB08716, GEB08751, GEB08725, GEB08767, GEB08944, GEB08911, GEB08912, GEB09026, GEB08985, GEB09003, GEB09025, GEB08937, GEB08913, GEB09005, GEB09011, GEB09017, GEB09004, GEB09027, GEB09006, GEB08915, GEA04108, GEA03972, GEA04945, GEA04356, GEA04109, GEA03971, GEA04343, GEA04120, GEA04122, GEA04001, GEA04321, GEA04954, GEA04106, GEA03999, GEA04319, GEA04000, GEA04955, GEA04046, GEA05002, GEA03973, GEA04965, GEA04953, GEA04346, GEA04049, GEA04967, GEA04119, GEA03998, GEA04048, GEA04964, GEA04966, GEA05001, GEA04322, GEA04357, GEA04237, GEA04235, GEA04047, GEA04107, GEA04944, GEA05003, GEA03970, GEA04238, GEA04946, GEA04121, GEA04355, GEA05004, GEA04344, GEA04358, GEA04345, GEA04952, GEA03342, GEA03345, GEA03556, GEA03514, GEA03538, GEA03166, GEA03188, GEA03159, GEA03554, GEA03542, GEA03541, GEA03170, GEA03268, GEA03168, GEA03186, GEA07644, GEA07359, GEA07642, GEA07360, GEA07734, GEA07744, GEA07715, GEA07636, GEA07381, GE021410, GE021526, GE021574, GEA03344, GEA03321, GEA03540, GEA03079, GEA03549, GEA03080, GEA03160, GEA03158, GEA03173, GEA03069, GEA03266, GEA03269, GEA03516, GEA03508, GEA03531, GEA03513, GEA03543, GEA03545, 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GEA07494, GEA08212, GEA08134, GEA08065, GEA08052, GEA08129, GEA08014, GEA08053, GEA07939, GEA06968, GEA07931, GEA06754, GEA07026, GEA08207, GEA08051, GEA08018, GEA08016, GEA07929, GEA08299, GEA07936, GEA08211, GEA07971, GEA08147, GEA08013, GEA08027, GEA08024, GEA08097, GEA08096, GEA08248, GEA08253, GEA08094, GEA07908, GEA08089, GEA08251, GEA08109, GEA08250, GEA08090, GEA08122, GEA03051

Recall status

Ongoing — the recall is still being carried out.

Where it was distributed

Worldwide

Recall record

Recalling firm: Datex-Ohmeda, Inc.
Product type: Devices
Recall number: Z-0776-2024
Voluntary / mandated: Voluntary: Firm initiated
Initial notification: Letter
Origin: Madison, WI
Recall initiated: 2023-12-29

What to do

Check the lot/code above against your product. To confirm this record and read the FDA's full notice, see the FDA recall page. Before changing anything you take or use, ask your pharmacist or prescriber — this page does not tell you to start or stop any drug or device.

Also available: structured data (JSON-LD) · recall record (JSON)

What this is — and is not

A recall is a recorded FDA enforcement action — the FDA logged that a firm is removing or correcting a product. It does not establish that any specific unit harmed anyone, and causation is not established by a recall. The class above is the FDA's risk judgment for the product category, not a finding about your unit. This page informs and compares; it is not medical advice and never tells you to start or stop a drug or device.

To report a problem you experienced, use FDA MedWatch. Verify this record at FDA recalls · Recall Z-0776-2024 · Source: openFDA enforcement.