Recall Register

Food, drugs, devices › Firms

Instrumentation Industries Inc

FDA recalling firm · 3 enforcement events · 3 product records · 2012–2015 · PA

Instrumentation Industries Inc has 3 FDA enforcement events on this register (3 product records) between 2012 and 2015: 3 device; the busiest year was 2012 with 1.

0% of its events are Class I; the most common class is Class II (3). 0 events are listed as ongoing; the recalling firm's address is in PA.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

InitiatedProduct (first record)TypeClassRecordsStatus
23 Sep 2015Ventilator TubingDeviceClass II1Terminated
13 Nov 2013RTC 25-C Inline Aerosol Tee Adapter. Intended to be used to adapt an aerosolized medication delivery system having an elliptical mouthpiece to a ventilator circuit.DeviceClass II1Terminated
7 Sep 2012Instrumentation Industries BE183-SU and BE 183 SU-12 Manual Jet Ventilators; BE 183-SUR and BE 183 SUR-12 Manual Jet Ventilators with Regulator and Gauge; BE 183-2 4 ft. Small Bore Tubing Assembly w/Inline Filter; and BE 183-R Regulator The BE 183-SUR and BE 183-SU Manual Jet Ventilators are designed to provide…DeviceClass II1Terminated

By type and class

Device3
Class II3

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

12
14
16
18
20
22
24
26
Enforcement events for Instrumentation Industries Inc by year initiated.

Questions and answers

How many FDA recalls has Instrumentation Industries Inc had?

3 enforcement events (3 product records) on this register, 2012–2015: 3 device.

Are any Instrumentation Industries Inc recalls ongoing?

0 events are listed as ongoing in the current openFDA export.

What class are Instrumentation Industries Inc recalls?

3 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.