VentStar Anesthesia WT recall
VentStar Anesthesia WT (P)180, MP00374
Why was VentStar Anesthesia WT 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: 04048675421948; All lots.
- Product
- VentStar Anesthesia WT (P)180, MP00374
- Recalling firm
- Draeger Medical, Inc.
- Quantity
- 130 units
- Distribution
- Domestic: US Nationwide Distribution.
- Recall date
- May 24, 2023
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (device)