VentStar Watertrap recall
VentStar Watertrap (P) 180, MP00361
Why was VentStar Watertrap recalled?
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
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?
UDI-DI: 04048675422013; All lots.
- Product
- VentStar Watertrap (P) 180, MP00361
- Recalling firm
- Draeger Medical, Inc.
- Quantity
- 50 units
- Distribution
- Domestic: US Nationwide Distribution.
- Recall date
- May 24, 2023
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (device)