INSTRUMENTATION INDUSTRIES, INCORPORATED
3 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (3)
- Inspections (2)
Devices registered here (1)
- Ventilator, Continuous, Facility UseProduct code CBK (opens in a new tab) · Class II · Anesthesiology · 21 CFR 868.5895
Recalls & enforcement
- Class IITerminated2015-09-23As a distributor of tubing manufactured by Smooth Bore Plastics, we are initiating a product recall for specific lots of KC 036, KC 060 and KC 072 reusable ventilator tubes due to a possible manufacturing defect: A few tubes may have the potential for delamination to occur betwe…
- Class IITerminated2013-11-13Some packages of the RTC 25-C may have been shipped to customers with incomplete Installation and Usage Directions due to a printing error.
- Class IITerminated2012-09-07Firm initiated an update to Directions for Use necessitating replacement of previously distributed Directions for Use.
FDA inspections (2)
- NAI2021-12-13No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
- VAI2016-03-15Voluntary 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. “INSTRUMENTATION INDUSTRIES, INCORPORATED (FEI 2518436) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/2518436-instrumentation-industries-incorporated/
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