Arrow Pressure Injectable Arrowg+ard Blue Plus¿ recall
Arrow Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC, REF CDC-45854-P1A; catheter, intravascular, therapeutic, long-term greater than 30…
Why was Arrow Pressure Injectable Arrowg+ard Blue Plus¿ recalled?
This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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?
Batch/Lot number 13F22L0806
- Product
- Arrow Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC, REF CDC-45854-P1A; catheter, intravascular, therapeutic, long-term greater than 30…
- Recalling firm
- ARROW INTERNATIONAL Inc.
- Quantity
- 380 units
- Distribution
- US
- Recall date
- October 11, 2023
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)