Arterial Catheterization Kit recall: Sterility Concern
Arterial Catheterization Kit, Arterial Line Kit with Sharps Safety Features wire, guide, catheter The Arrow Arterial Catheterization device permits…
Why was Arterial Catheterization Kit recalled?
Arrow International is recalling the affected product because the packaging may not be completely sealed, which may compromise sterility.
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?
Material number: ASK-04018-CC, ASK-04510-HUM, ASK-04550-UHC, Device Listing D025180
- Product
- Arterial Catheterization Kit, Arterial Line Kit with Sharps Safety Features wire, guide, catheter The Arrow Arterial Catheterization device permits…
- Recalling firm
- Arrow International Inc
- Quantity
- 27, 485 distributed in the U.S, 4,371 distributed Internationally
- Distribution
- Worldwide Distribution - US (nationwide) and Canada
- Recall date
- June 21, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)