Pressure Injectable Arrowg+ard Blue Plus Multi-Lumen recall
Pressure Injectable Arrowg+ard Blue Plus Multi-Lumen Central Venous Catheterization Kit. Permits venous access to central circulation by way of…
Why was Pressure Injectable Arrowg+ard Blue Plus Multi-Lumen recalled?
Arrow International is recalling due to possible voids in the catheter hub, which could lead to an interlumen crossover.
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 Codes ASK-45703-PRWJ1, ASK-45703-PUAB1, and ASK-45703-PUPM Lot # 13F16L0105, 23F16K0180 and 13F16L0199
- Product
- Pressure Injectable Arrowg+ard Blue Plus Multi-Lumen Central Venous Catheterization Kit. Permits venous access to central circulation by way of…
- Recalling firm
- Arrow International Inc
- Quantity
- 310 units
- Distribution
- US Distribution to NJ, IL, and PA
- Recall date
- May 3, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)