Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
RespVent Closed Suction System T-Piece Tracheostomy Adult Recalled by RESPIRATORY THERAPEUTICS GROUP LLC Due to It has been determined that some units of...
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 RESPIRATORY THERAPEUTICS GROUP LLC directly.
Affected Products
RespVent Closed Suction System T-Piece Tracheostomy Adult, Diameter: 4.6mm (14F), Length: 30.5cm (12in.), MDI Adapter, Cont. 10 Closed Suction Catheter, Sterile R, RxOnly, Reorder Number: RTG-02300, UDI: 00850108006035 - Product Usage: To be used to aspirate liquids or semi solids from a patient s upper airway.
Quantity: 723 cases (7230 units)
Why Was This Recalled?
It has been determined that some units of catheters were not tightly connected to the thumb port. This may result in the catheter disconnecting from the thumb port which could reduce the suction performance and make it difficult to remove from the patient's trachea.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About RESPIRATORY THERAPEUTICS GROUP LLC
RESPIRATORY THERAPEUTICS GROUP LLC has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report