FDA Medical Device Recalls (openFDA)
Allison Medical, Inc.: InControl Insulin Syringes, Short Needle, 29 Gauge, 1CC
- Recall number
- Z-0266-2023
- Recalling firm
- Allison Medical, Inc.
- Product
- InControl Insulin Syringes, Short Needle, 29 Gauge, 1CC
- Status
- Completed
- Initiated
- 2018-01-19
- Posted
- 2022-11-18
- Terminated
- not on file
- Reason
- Insulin syringe retail packages incorrectly labeled as "Short Needle".
- Root cause
- Error in labeling
- Action
- On 01/19/2018, The recalling firm notified their customer of the recall.
- Quantity
- 1,500 Boxes (150,000 syringes)
- Distribution
- Texas
- Lot, serial or model codes
- UDI/Lot/Expiration: 00041220791484/ 170407/ 2022-03-31
- 510(k) numbers
- ["K191531"]
- PMA numbers
- not on file
- Product code
- FMF
- Firm FEI
- 1000138447
- Firm city
- Littleton
- Firm state
- CO
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28