FDA Device recall Z-2047-2019
Monoject" 201 Vet Pak Hypodermic Needle, 16 ga x 1-1/2 Item code: 8881201654
- FDA Device
- Class II
- completed
- Published 2019-07-31
On 2019-07-31 the FDA classified a Class II recall of Monoject" 201 Vet Pak Hypodermic Needle, 16 ga x 1-1/2 Item code: 8881201654 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-2047-2019 |
| 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" 201 Vet Pak Hypodermic Needle, 16 ga x 1-1/2 Item code: 8881201654
Reason
Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
Identifiers
| code_info | Lot Number: 902108 |
|---|
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-2047-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.