Distal Phasitron recall
Distal Phasitron, Part: S20020, for use with Percussionaire VDR-4 control driver (or control unit)
Why was Distal Phasitron recalled?
Breathing circuit reservoir bag may be assembled at the wrong attachment point, which will result in less than optimal therapy.
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?
UDI-DI: 00849436000693, Lots/Expiration: WO03739/September 13, 2024, and WO04218/November 14, 2024.
- Product
- Distal Phasitron, Part: S20020, for use with Percussionaire VDR-4 control driver (or control unit)
- Recalling firm
- Percussionaire Corporation
- Quantity
- 195
- Distribution
- US: RI, CA, TX
- Recall date
- January 24, 2024
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)