FDA Device recall Z-0846-2022
BALLARD* Multi-Access Port Catheter, Double Swivel Y Elbow, Adult, 14 French
- FDA Device
- Class II
- terminated
- Published 2022-04-06
On 2022-04-06 the FDA classified a Class II recall of BALLARD* Multi-Access Port Catheter, Double Swivel Y Elbow, Adult, 14 French by Avanos Medical, citing product was distributed with incorrect expiration date.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0846-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-11-22 |
| Published | 2022-04-06 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Avanos Medical |
| Distribution | US |
Product
BALLARD* Multi-Access Port Catheter, Double Swivel Y Elbow, Adult, 14 French; Sterile; Single Use
Reason
Product was distributed with incorrect expiration date.
Identifiers
| code_info | Finished Product Code: 102005202; Alternate Code: 24014-5; Lot No.: 20065842, 30135996, 30135999, 30137463, 30140309, 30138711, and 30141360. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0846-2022%22
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