Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
VORTRAN Automatic Resuscitator Recalled by Vortran Medical Technology 1, Inc Due to Vortran received a customer complaint that the spin-nut-DSS...
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 Vortran Medical Technology 1, Inc directly.
Affected Products
VORTRAN Automatic Resuscitator, VARPlus; Model PTE-5002; Qty: 10 each Anesthesiology: This device is to be used by properly trained personnel to deliver emergency, short term, constant flow, pressure cycled ventilatory support.
Quantity: 35 cases (10 each)
Why Was This Recalled?
Vortran received a customer complaint that the spin-nut-DSS connector was assembled in the reverse direction on the oxygen tubing; making the connector unable to be screwed on due to the wrong thread direction.
Where Was This Sold?
This product was distributed to 3 states: CA, FL, MS
About Vortran Medical Technology 1, Inc
Vortran Medical Technology 1, Inc has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report