Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Parker Left Double Lumen Endobronchial Tube with Parker Flex-Tip (Parker Recalled by Parker Medical Due to The product was not functioning as intended. The...
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 Parker Medical directly.
Affected Products
Parker Left Double Lumen Endobronchial Tube with Parker Flex-Tip (Parker Endo-Bronch with Flex Tip). Model Numbers: H-PFTDL-28-1, H-PFTDL-32-1, H-PFTDL-35-1, H-PFTDL-37-1, H-PFTDL-39-1, H-PFTDL-41-1. The product is an endotracheal tube with a double lumen for single lung isolation allowing for ventilation of one lung during a surgical procedure. Endotracheal tubes are used for intubating patients and used in conjunction with a ventilator to provide oxygen and anesthetic agents to the patient during surgeries
Quantity: 1,060 units
Why Was This Recalled?
The product was not functioning as intended. The ventilation to the patient was not disrupted, but the single lung isolation and ventilation did not function as intended.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Parker Medical
Parker Medical 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