CLASS II Device recall · Reported 30 Nov 2022 · FDA Enforcement Report
InControl Insulin Syringes, Short Needle, 1CC recalled
Allison Medical is recalling InControl Insulin Syringes, Short Needle, 1CC, distributed in Texas. The recall was initiated on 19 Jan 2018 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-0266-2023
- FDA event ID
- 91083
- Recalling firm
- Allison Medical, Littleton, CO
- Classification
- Class II
- Status
- Completed
- Recall initiated
- 19 Jan 2018
- FDA classified
- 18 Nov 2022
- Reported
- 30 Nov 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Labeling Errors
- Device type
- Syringes & Needles
Timeline
| 19 Jan 2018 | Recall initiated by company | |
| 18 Nov 2022 | Classified by FDA | +1764 days |
| 30 Nov 2022 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Insulin syringe retail packages incorrectly labeled as "Short Needle".
Product as listed by the FDA
InControl Insulin Syringes, Short Needle, 29 Gauge, 1CC
Where it was distributed
Texas
Questions about this recall
Why was it recalled?
Insulin syringe retail packages incorrectly labeled as "Short Needle".
Which lots are affected?
UDI/Lot/Expiration: 00041220791484/ 170407/ 2022-03-31
Where was it sold?
Texas
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Allison Medical
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | CarePoint Syringe Without Needle recalled by Allison Medical | Allison Medical | Potency & Assay | 5 states |
Other Syringes & Needles recalls
All 1,060| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS I | BD Needle Kit for Powered Driver recalled by Bard Access Systems | Bard Access Systems | Other | 32 states |
| Device | CLASS II | Boston Scientific Enhance Transcarotid/Peripheral Access Kit recalled | Galt Medical | Other | Nationwide |
| Device | CLASS II | Geneva Brachytherapy Applicator recalled by Elekta | Elekta | Other | Nationwide |
| Device | CLASS II | Brachytherapy Applicator Advanced Gynecological Applicator recalled | Elekta | Other | Nationwide |
| Device | CLASS II | Medline 111 Gravity Set W/3 Needle Free Y-Sites recalled | BD Switzerland Sarl | Other | IL |