FDA Device recall Z-0196-2020
DEMO No Needle Corrugated Carton 30 U/D, Part Number 2260-02
- FDA Device
- Class II
- terminated
- Published 2019-11-06
On 2019-11-06 the FDA classified a Class II recall of DEMO No Needle Corrugated Carton 30 U/D, Part Number 2260-02 by Valeritas, citing there is a potential for "No Needle Demo Units" to contain a needle.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0196-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-07-03 |
| Published | 2019-11-06 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Valeritas |
| Distribution | US |
Product
DEMO No Needle Corrugated Carton 30 U/D, Part Number 2260-02
Reason
There is a potential for "No Needle Demo Units" to contain a needle.
Identifiers
| code_info | UDI: (01)10385609020022(17)XXXXXX(10)XXXXXXXX Lot Numbers: DM318007 DM318008 DM318009 DM318010 DM318026 |
|---|
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-0196-2020%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.