Recall Z-2357-2026
Datex-Ohmeda Inc · initiated May 8, 2026
Class I – dangerous or defective products that could cause serious health problems or death
Product
Giraffe Stand-alone Infant Resuscitation System; Powered emergency ventilator (resuscitator) Product identifiers: 2082663-001, 2082663-002, M1241424 Product impacted only if service blender M1091607-R was installed during the last Preventative Maintenance
Codes / lots: UDI-DI of service blender component: 00813841020010 Affected devices were installed with the following serial numbers of affected service blender components: 002I08B 002X08B 008S10B 008Y09B 013S09B 016A09B 016R09B 018P10B 019J09B 028C08B 02X08B 033N09B 037E08B 038D10B 038N08B 042F10B 042S10B 042T10B 045808B 045M08B 047I08B 047J08B 054C10B 054I10B 054L10B 054N09B 054O09B 054U10B 055D09B 055V09B 057908B 061K09B 062C10B 068W10B 077M09B 078509B 078M09B 078S09B 084I10B 084J10B 092G08B 099F08B 1 B1405629 100E08B 100R08B 104A09B 12105790 133D08B 136708B 136W08B 141J09B 142009B 142W09B 144J08B 144N08B 149Q09B 163608B 169D08B 169G08B 169H08B 172308B 175P08B 185I08B 185Q08B 186208B 189808B 189A09B 189C08B 189F09B 193L08B 193N08B 195D09B 195E09B 195J09B 195K09B 198H08B 210K09B 210U09B 218N09B 219C09B 219K09B 220E08B 226F08B 244L09B 260X09B 266M08B 267808B 280F09B 281H09B 285J07B 295H09B 295J09B 295P08B 310I09B 338707B 338E07B 338K07B 352Y09B 355P09B 7979700385 B1003093 B1003112 B1003124 B1003140 B1003143 B1003147 B1003153 B1003343 B1003452 B1003550 B1003867 B1003944 B1004844 B1004861 B1004924 B1005029 B1005036 B1005044 B1005422 B1005534 B1005560 B1005571 B1005839 B1006102 B1006113 B1006304…
Reason for recall
Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the intended concentration set by the user, potentially resulting in hypoxia or hyperoxia in the patient.
FDA-determined cause: Process control
Action taken
Firm began notifying customers on 5/8/2026 via letters titled "URGENT MEDICAL DEVICE CORRECTION." Customers were instructed to identify affected devices by following instructions provided in the letter. Devices with affected blenders should be removed from patient use, and the customer should contact a GE HealthCare Service Representative.
Details
- Recall number
- Z-2357-2026
- Initiated
- May 8, 2026
- Posted by FDA
- June 18, 2026
- Product code
- BTM – Ventilator, Emergency, Manual (Resuscitator)
- Quantity
- 550 (367 US; 183 OUS)
- Distribution
- Pending
- Recalling firm
- Datex-Ohmeda Inc, Waukesha, WI
Other products in the same recall event
| Recall | Product | Initiated |
|---|---|---|
| Z-2358-2026 Class I | Giraffe Warmer with Integrated Resuscitation System (iRes), Panda Warmer with Integrated…Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver… | 05/08/2026Open, Classified |
| Z-2359-2026 Class I | Panda Freestanding Warmer, Infant Radiant Warmer Product Identifiers: 2063568-001…Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver… | 05/08/2026Open, Classified |