InControl Insulin Syringes, Short Needle, 29 Gauge, 1CC recallZ-0266-2023 · Allison Medical, Inc. · initiated Jan 19, 2018
Completed
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Allison Medical, Inc. or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Insulin syringe retail packages incorrectly labeled as "Short Needle".
FDA root cause category: Error in labeling
What the company is doing
On 01/19/2018, The recalling firm notified their customer of the recall.
Recall details
- Recall number
- Z-0266-2023
- Status
- Completed
- Initiated by the company
- Jan 19, 2018
- Posted by the FDA
- Nov 18, 2022
- Recalling firm
- Allison Medical, Inc.
- Quantity
- 1,500 Boxes (150,000 syringes)
- Product code
- FMF
- FDA submissions
- K191531
- Distribution
- Texas
Product description
InControl Insulin Syringes, Short Needle, 29 Gauge, 1CC
Code information (models, lots, serial numbers)
UDI/Lot/Expiration: 00041220791484/ 170407/ 2022-03-31
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- HEB In-Control Insulin Syringe 79148H. E. Butt Grocery Company · Needle, Hypodermic, Single Lumen1 recall0 reports
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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