Arrow Endurance" Extended Dwell Peripheral Catheter recall: Sterility Concern
Arrow Endurance" Extended Dwell Peripheral Catheter System, REF: ASK-00820-FLH
Why was Arrow Endurance" Extended Dwell Peripheral Catheter recalled?
Potential sterility issue for specific lots of the Arrow Endurance" Extended Dwell Peripheral Catheter System, Product Code ASK-00820-FLH.
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?
REF: ASK-00820-FLH Manufacturing Lots: 13F19E0247, 13F19F0006, and 13F19G0433 Exp. Date: Aug. 2020 - Sep. 2020
- Product
- Arrow Endurance" Extended Dwell Peripheral Catheter System, REF: ASK-00820-FLH
- Recalling firm
- Arrow International Inc
- Quantity
- 575
- Distribution
- US: FL
- Recall date
- January 29, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)