Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MILEX OMNIFLEX DIAPHRAGM SIZE 80 Model: MXWF80 Recalled by CooperSurgical, Inc. Due to A diaphragm size 80 labeled box was incorrectly...
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 CooperSurgical, Inc. directly.
Affected Products
MILEX OMNIFLEX DIAPHRAGM SIZE 80 Model: MXWF80
Quantity: 200 units
Why Was This Recalled?
A diaphragm size 80 labeled box was incorrectly packaged with a size 85.
Where Was This Sold?
This product was distributed to 15 states: AK, CA, FL, IL, ME, MT, NE, NJ, NM, NY, OK, OR, VA, WI, DC
About CooperSurgical, Inc.
CooperSurgical, Inc. has 83 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report