FDA Device recall Z-1347-2021
Enteral Infusion Pump
- FDA Device
- Class II
- completed
- Published 2021-04-14
On 2021-04-14 the FDA classified a Class II recall of Enteral Infusion Pump by Cardinal Health 200, citing the potential for air appearing in the enteral feed pumping set tubing during set-up.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1347-2021 |
| Classification | Class II |
| Status | completed |
| Initiated | 2021-01-19 |
| Published | 2021-04-14 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Cardinal Health 200 |
| Distribution | US |
Product
Enteral Infusion Pump
Reason
The potential for air appearing in the enteral feed pumping set tubing during set-up.
Identifiers
| code_info | Catalog Number: 612054, 613650, 614650, 672055, 673656, 673662, 674655, 674668, 674669, 716154, 762055, 763656, 763662,…Catalog Number: 612054, 613650, 614650, 672055, 673656, 673662, 674655, 674668, 674669, 716154, 762055, 763656, 763662, 765100, 765559, 772055, 773656, 773662, 775100, 775659, 776150 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1347-2021%22
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