ID Circuit Watertrap recall
ID Circuit Watertrap (P) 180, Catalog Number MP01341 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of…
Why was ID Circuit Watertrap recalled?
Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit
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?
All Lots
- Product
- ID Circuit Watertrap (P) 180, Catalog Number MP01341 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of…
- Recalling firm
- Draeger Medical, Inc.
- Quantity
- 25 units
- Distribution
- US Distribution to states of: AL, CA, CO, CT, FL, KY, MI, NJ, OH, PA, SC & TX.
- Recall date
- January 30, 2019
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (device)