ARROWg+ard Blue PLUS Pressure Injectable Two-Lumen CVC recall: Foreign Material
ARROWg+ard Blue PLUS Pressure Injectable Two-Lumen CVC Kit. The Multiple-Lumen Catheter permits venous access to the central circulation by way of the…
Why was ARROWg+ard Blue PLUS Pressure Injectable Two-Lumen CVC recalled?
Foreign material found within the kits. The foreign material, white or black particles and/or thread, is visible and can beidentified by the user.
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?
product number CDC-42802-P1A, lot number 23F14A0063
- Product
- ARROWg+ard Blue PLUS Pressure Injectable Two-Lumen CVC Kit. The Multiple-Lumen Catheter permits venous access to the central circulation by way of the…
- Recalling firm
- Arrow International Inc
- Quantity
- 1195
- Distribution
- Nationwide
- Recall date
- February 18, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)