Class II — Allison Medical, Inc.
| Recalling firm | ALLISON MEDICAL, INC. |
|---|---|
| Registered facility | ALLISON MEDICAL, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Completed |
| Reason | Insulin syringe retail packages incorrectly labeled as "Short Needle". |
| Product | InControl Insulin Syringes, Short Needle, 29 Gauge, 1CC |
| Quantity | 1,500 Boxes (150,000 syringes) |
| Distribution | Texas |
| Initiated | 2018-01-19 |
| Classified | 2022-11-18 |
| Recall number | Z-0266-2023 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Allison Medical, Inc. (Z-0266-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/91083/
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