Pneupac paraPac plus 300 ventilator kit recall
Pneupac paraPac plus 300 ventilator kit, REF P300NGB
Why was Pneupac paraPac plus 300 ventilator kit recalled?
Two devices were labeled with the same serial number
What should I do if I have this product?
Review the official FDA enforcement record for current 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?
SN RF70121
- Product
- Pneupac paraPac plus 300 ventilator kit, REF P300NGB
- Recalling firm
- Smiths Medical ASD Inc.
- Quantity
- 2 units
- Distribution
- UK
- Recall date
- November 3, 2021
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)