The CG+ Arrow PIC Catheters permit venous access to the recall: Labeling Error
The CG+ Arrow PIC Catheters permit venous access to the central circulation through a peripheral vein.
Why was The CG+ Arrow PIC Catheters permit venous access to the recalled?
Arrow International, Inc. notified its customers who received the affected Antimicrobial/Antithrombogenic PICC Kits, that the kits were being recalled due to a labeling error. The lidstock on some of the kits reads CDC-45541-HPK1A, while the banner card on the side of the kit reads CDC-45052-HPK1A. Other kits may list CDC-45052-HPK1A on the lidstock and CDC-45541-HPK1A on the banner card. The affected lot numbers are 23F16C0851, 23F16A0727, and 23F16C0844.
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?
Device Listing Number: D149129 Lot Numbers: 23F16C0851, 23F16A0727 and 23F16C0844
- Product
- The CG+ Arrow PIC Catheters permit venous access to the central circulation through a peripheral vein.
- Recalling firm
- Arrow International Inc
- Quantity
- 1,351 catheters
- Distribution
- US Distribution
- Recall date
- April 12, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)