FDA Device recall Z-2973-2024
Pneupac paraPAC plus 300 ventilator kit, REF P300NXX
- FDA Device
- Class I
- ongoing
- Published 2024-09-18
On 2024-09-18 the FDA classified a Class I recall of Pneupac paraPAC plus 300 ventilator kit, REF P300NXX by Smiths Medical Asd, citing there is a potential for inadvertent tidal volume knob movement from the original setting when set at high (1000-1500 mL) and low (70-150 mL) settings.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2973-2024 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2024-05-31 |
| Published | 2024-09-18 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Smiths Medical Asd |
| Distribution | n/a |
Product
Pneupac paraPAC plus 300 ventilator kit, REF P300NXX
Reason
There is a potential for inadvertent tidal volume knob movement from the original setting when set at high (1000-1500 mL) and low (70-150 mL) settings.
Identifiers
| code_info | All Serial Numbers. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2973-2024%22
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