Pneupac paraPAC plus 310 ventilator kit with PEEP and recall
Pneupac paraPAC plus 310 ventilator kit with PEEP and CPAP, REF P310NXX
Why was Pneupac paraPAC plus 310 ventilator kit with PEEP and recalled?
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.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
All serial numbers
- Product
- Pneupac paraPAC plus 310 ventilator kit with PEEP and CPAP, REF P310NXX
- Recalling firm
- Smiths Medical ASD Inc.
- Quantity
- 10,240 units
- Distribution
- Worldwide
- Recall date
- September 18, 2024
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)