PROCEDURE PRODUCTS, INC.
1 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (1)
- Inspections (1)
Devices registered here (1)
- Container, I.V.Product code KPE (opens in a new tab) · Class II · General Hospital · 21 CFR 880.5025
Recalls & enforcement
- Class IITerminated2015-10-27The firm had received a complaint alleging that a medical professional had difficulty inserting a guide wire into a needle
FDA inspections (1)
- NAI2018-06-07No Action Indicated · Compliance: Devices; Postmarket Assurance: 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. “PROCEDURE PRODUCTS, INC. (FEI 3020778) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3020778-procedure-products-inc/
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