Radial Artery Catheterization Kit recall
Radial Artery Catheterization Kit; Model: AK-04122
Why was Radial Artery Catheterization Kit recalled?
The povidone iodine prep pads included in certain kits and trays do not meet the requirements for a 36-month shelf life and should be labeled with a 24-month shelf life.
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?
Lots: 13F16H0329, 13F17F0074, 13F17G0237; Expiration dates: October 2018 through March 2020
- Product
- Radial Artery Catheterization Kit; Model: AK-04122
- Recalling firm
- Arrow International Inc
- Quantity
- 570
- Distribution
- US nationwide distribution, including Puerto Rico.
- Recall date
- April 11, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)