Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
VITRIGUARD Recalled by CooperSurgical, Inc. Due to Products in this lot may have compromised barrier...
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
VITRIGUARD, CARRIER, CLEAR; Model. No. 43782001 The VitriGuard device is a cryopreservation storage device composed of a stick and cap.
Quantity: 2,340 (US only)
Why Was This Recalled?
Products in this lot may have compromised barrier seals, introducing a risk to sterility.
Where Was This Sold?
This product was distributed to 10 states: AZ, CA, FL, IL, MI, MO, NY, OR, TX, WV
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