FDA Device recall Z-0285-2020
13 Fr. Trialysis Catheter with Alphacurve
- FDA Device
- Class II
- terminated
- Published 2019-11-13
On 2019-11-13 the FDA classified a Class II recall of 13 Fr. Trialysis Catheter with Alphacurve by Becton Dickinson And, citing A portion of the lot was incorrectly packaged with a 12.5cm catheter instead of a 15cm catheter.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0285-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-09-16 |
| Published | 2019-11-13 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Becton Dickinson And |
| Distribution | AR, FL, IL, NJ, TX, WI |
Product
13 Fr. Trialysis Catheter with Alphacurve. Catalog No. 5653150. UDI: 00801741066023 Power-Trialysis Short-Term Alphacurve Dialysis Catheter with a third internal umen for IV therapy, power injection of contrast media, and central venous pressure monitoring.
Reason
A portion of the lot was incorrectly packaged with a 12.5cm catheter instead of a 15cm catheter.
Identifiers
| code_info | REDR0440 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0285-2020%22
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