ARROW ENDURANCE" Extended Dwell Peripheral Catheter recall
ARROW ENDURANCE" Extended Dwell Peripheral Catheter System, Catalog Numbers: EDC-00820 & EDC-00820-B
Why was ARROW ENDURANCE" Extended Dwell Peripheral Catheter recalled?
Certain lots of peripheral catheter systems may be missing the safety latch, intended to minimize the risk of sharps injuries.
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?
Catalog Number: EDC-00820, Lot: 14X17C0039 (Expires February 2019); Catalog Number: EDC-00820-B, Lot: 13F17F0120 (Expires May 2019)
- Product
- ARROW ENDURANCE" Extended Dwell Peripheral Catheter System, Catalog Numbers: EDC-00820 & EDC-00820-B
- Recalling firm
- Arrow International Inc
- Quantity
- 305
- Distribution
- Distributed in the following U.S. states: CO, FL, IL, NC, PA, SC, and TX.
- Recall date
- April 4, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)