Single Transpac IT Monitoring Kit w/03 ml Flush Device recall
Single Transpac IT Monitoring Kit w/03 ml Flush Device, Needleless Valve, Macrodrip, Item No. 011-46106-29 Transpac Trifurcated monitoring kit with…
Why was Single Transpac IT Monitoring Kit w/03 ml Flush Device recalled?
ICU has become aware of an issue with a component where the connection on an arterial monitoring kit may crack and cause a fluid leak.
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?
Lot No. 2866991
- Product
- Single Transpac IT Monitoring Kit w/03 ml Flush Device, Needleless Valve, Macrodrip, Item No. 011-46106-29 Transpac Trifurcated monitoring kit with…
- Recalling firm
- ICU Medical, Inc.
- Quantity
- 200 units
- Distribution
- Worldwide Distribution - USA including Oregon and Internationally to Australia.
- Recall date
- August 13, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)