InControl Insulin Syringes — Class II medical device recall Z-0266-2023
Completed recall by Allison Medical, Inc., reported 2022-11-30, distributed in TX. Insulin syringe retail packages incorrectly labeled as "Short Needle".
| Recall number | Z-0266-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Allison Medical, Inc., Littleton, CO, United States |
| Recall initiated | 2018-01-19 |
| Classified | 2022-11-18 |
| Reported by FDA | 2022-11-30 |
| Distributed | TX |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00041220791484 |
| Lot numbers | 170407 |
Product
InControl Insulin Syringes, Short Needle, 29 Gauge, 1CC
Reason for recall
Insulin syringe retail packages incorrectly labeled as "Short Needle".
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0266-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.