Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Puritan Bennett Cuff Pressure Manager Recalled by Covidien Due to Inadequate internal fixation of the power inlet port...
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 Covidien directly.
Affected Products
Puritan Bennett Cuff Pressure Manager, REF: 180-03
Quantity: 408
Why Was This Recalled?
Inadequate internal fixation of the power inlet port to the cuff pressure manager device causes the external power inlet to became dislodged within the device housing after several uses, which prevents the device from being charged, and could lead to treatment delay.
Where Was This Sold?
This product was distributed to 16 states: AL, AZ, CA, CO, FL, IL, KS, KY, MA, MI, NJ, NY, NC, TN, TX, UT
About Covidien
Covidien has 21 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report