Pressure Injectable Multi- Lumen Central Venous recall
Pressure Injectable Multi- Lumen Central Venous Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology Product Usage: The Arrow¿ CVC is…
Why was Pressure Injectable Multi- Lumen Central Venous recalled?
Some of the products listed in the recall may be missing a sticker that contains the lot number, expiration date, and Unique Device Identification (UDI) information.
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?
ASK-45552-RWJ4 13F16J0286 13F16L0014 13F17A0217 13F17D0222 13F17E0849 13F17F0784 13F17G0413
- Product
- Pressure Injectable Multi- Lumen Central Venous Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology Product Usage: The Arrow¿ CVC is…
- Recalling firm
- Arrow International Inc
- Quantity
- 23,904 in total
- Distribution
- US in the states of OH, FL, SC, TX, KY, NJ, MI
- Recall date
- March 21, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)