Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Instrumentation Industries BE183-SU and BE 183 SU-12 Manual Jet Ventilators Recalled by Instrumentation Industries Inc Due to Firm initiated an update to Directions for Use...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Instrumentation Industries Inc directly.
Affected Products
Instrumentation 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 transtracheal ventilation in specific emergency situations of upper airway obstructions.
Quantity: 2998
Why Was This Recalled?
Firm initiated an update to Directions for Use necessitating replacement of previously distributed Directions for Use.
Where Was This Sold?
This product was distributed to 43 states: AL, AK, AZ, CA, CO, CT, FL, GA, ID, IL, IN, IA, KS, KY, LA, MD, MA, MI, MN, MS, MO, MT, NV, NH, NJ, NY, NC, ND, OH, OK, OR, PA, SC, SD, TN, TX, UT, VT, VA, WA, WV, WI, DC
About Instrumentation Industries Inc
Instrumentation Industries Inc has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report