Procedure Products, Inc.
1 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (1)
Registered facilities (1)
- PROCEDURE PRODUCTS, INC. FEI 3020778 · WA
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
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “Procedure Products, Inc. — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-3020778-procedure-products-inc/
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