Newport Medical Instruments Inc Newport HT50 All Purpose Ventilator Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Newport HT50 All Purpose Ventilator
Brand
Newport Medical Instruments Inc
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
All serial numbers. Products are identified by serial numbers on back of ventilators. Manufacturer states serial numbers of ventilators involved in field correction may be obtained through shipping records.
Newport Medical Instruments Inc is recalling Newport HT50 All Purpose Ventilator due to Lack of alarm prior to shutdown.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Lack of alarm prior to shutdown.
Recommended Action
Per FDA guidance
Notice of Field Correction was sent to consignees dated 10/29/2004. A second notice was sent 12/20/04 announcing that materials for conducting an upgrade were being sent which included a manual insert and brochure regarding the battery. Also request was made to return products as they are available. Notice was sent 12/20/04 that field correction kits were available for order. Recall is ongoing.
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 noticePage updated: Jan 10, 2026