Instrumentation Industries Inc BE 183 Series Manual Jet Ventilators. Manual Jet Ventilator Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
BE 183 Series Manual Jet Ventilators. Manual Jet Ventilator
Brand
Instrumentation Industries Inc
Lot Codes / Batch Numbers
Part number BE 183-SU, Lot number P0907203
Products Sold
Part number BE 183-SU, Lot number P0907203
Instrumentation Industries Inc is recalling BE 183 Series Manual Jet Ventilators. Manual Jet Ventilator due to possible external debris in the on/off plunger.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
possible external debris in the on/off plunger.
Recommended Action
Per FDA guidance
The recalling firm notified all customers via telephone to inform them of the problem and the need to return the product when received. The recalling firm issued recall letters dated 9/17/03 to their direct accounts informing them of the problem. The also informed the account that a stop shipment had been ordered but if they receive the product they need to return it immediately.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, FL, GA, IN, NY, OH, OR, TX, UT
Page updated: Jan 10, 2026