Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Lifesaver Single Patient Use Manual Resuscitator Product Usage: The Hudson Recalled by Teleflex Medical Due to The intake port may be blocked which can...
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 Teleflex Medical directly.
Affected Products
Lifesaver Single Patient Use Manual Resuscitator Product Usage: The Hudson RCI Lifesaver Single Patient Use manual resuscitator with pressure monitoring port is a disposable medical device intended for use on patients requiring temporary augmentation of ventilation with or without supplemental oxygen delivery during episodes of acute ventilatory failure or insufficiency.
Quantity: 9,333 units
Why Was This Recalled?
The intake port may be blocked which can cause the bag to fail to fill.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Teleflex Medical
Teleflex Medical has 204 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report