ALLISON MEDICAL, INC.
2 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (2)
- Inspections (3)
Devices registered here (1)
- Needle, Hypodermic, Single LumenProduct code FMI (opens in a new tab) · Class II · General Hospital · 21 CFR 880.5570
Recalls & enforcement
- Class IICompleted2020-09-03Syringe without needle may have a green substance on the plunger. Substance found to be nontoxic but its effect on drug potency or interaction is unknown.
- Class IICompleted2018-01-19Insulin syringe retail packages incorrectly labeled as "Short Needle".
FDA inspections (3)
- NAI2023-04-28No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
- VAI2022-07-29Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
- VAI2016-10-12Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “ALLISON MEDICAL, INC. (FEI 1000138447) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1000138447-allison-medical-inc/
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