FDA Device recall Z-0749-2013
Giraffe and Panda Bag and Mask Resuscitation System The T-piece Resuscitation System [ventilator, emergency powered resuscitator]/Panda Bag…
- FDA Device
- Class I
- terminated
- Published 2013-02-20
On 2013-02-20 the FDA classified a Class I recall of Giraffe and Panda Bag and Mask Resuscitation System The T-piece Resuscitation System [ventilator, emergency powered resuscitator]/Panda Bag… by Ge Healthcare, citing oxygen and air wall inlet fittings on the back panel of the resuscitation systems were reversed during assembly.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0749-2013 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2012-10-15 |
| Published | 2013-02-20 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Ge Healthcare |
| Distribution | AL, AZ, CA, CO, FL, GA, IA, ID, IL, KY, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NM, NV, NY, OH, OR, PA, TX, VT, WA, WI, WV |
Product
Giraffe and Panda Bag and Mask Resuscitation System The T-piece Resuscitation System [ventilator, emergency powered resuscitator]/Panda Bag and Mask Resuscitation System provides the basic equipment required for pulmonary resuscitation of infants.
Reason
Oxygen and air wall inlet fittings on the back panel of the resuscitation systems were reversed during assembly.
Identifiers
| code_info | Model M1139612 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0749-2013%22
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