FDA Device recall Z-2050-2019
Monoject Blunt Cannula, 19 G x 1-1/2" (1.067 mm x 3.8 cm) Item code: 8881202355
- FDA Device
- Class II
- completed
- Published 2019-07-31
On 2019-07-31 the FDA classified a Class II recall of Monoject Blunt Cannula, 19 G x 1-1/2" (1.067 mm x 3.8 cm) Item code: 8881202355 by Cardinal Health 200, citing manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2050-2019 |
| Classification | Class II |
| Status | completed |
| Initiated | 2019-04-30 |
| Published | 2019-07-31 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Cardinal Health 200 |
| Distribution | US |
Product
Monoject Blunt Cannula, 19 G x 1-1/2" (1.067 mm x 3.8 cm) Item code: 8881202355
Reason
Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
Identifiers
| code_info | Lot Number: 905617, 905618, 905619, 905620, 907004, 907005 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2050-2019%22
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