Bracco Injeneering S.A.
1 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (1)
- Inspections (1)
Devices registered here (1)
- Pump, Infusion Or Syringe, Extra-LuminalProduct code FIH (opens in a new tab) · Class II · Gastroenterology, Urology · 21 CFR 876.5820
Recalls & enforcement
- Class IITerminated2018-11-12Insufficient seal on the sterile barrier of the device, compromising the sterility of the device
FDA inspections (1)
- NAI2017-02-01No Action Indicated · Compliance: Devices
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. “Bracco Injeneering S.A. (FEI 3004753774) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3004753774-bracco-injeneering-s-a/
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