FDA Device recall Z-0266-2023
InControl Insulin Syringes, Short Needle, 29 Gauge, 1CC
- FDA Device
- Class II
- completed
- Published 2022-11-30
On 2022-11-30 the FDA classified a Class II recall of InControl Insulin Syringes, Short Needle, 29 Gauge, 1CC by Allison Medical, citing insulin syringe retail packages incorrectly labeled as "Short Needle".
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0266-2023 |
| Classification | Class II |
| Status | completed |
| Initiated | 2018-01-19 |
| Published | 2022-11-30 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Allison Medical |
| Distribution | TX |
Product
InControl Insulin Syringes, Short Needle, 29 Gauge, 1CC
Reason
Insulin syringe retail packages incorrectly labeled as "Short Needle".
Identifiers
| code_info | UDI/Lot/Expiration: 00041220791484/ 170407/ 2022-03-31 |
|---|
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-0266-2023%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.