Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Evicel Accessory Device - 45 cm Flexible Tip (SET OF 3) Recalled by Ethicon, Inc. Due to Products labeled for distribution outside the United States...
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 Ethicon, Inc. directly.
Affected Products
Evicel Accessory Device - 45 cm Flexible Tip (SET OF 3), Product Code EVT45. Accessory Tips for use only with EVICEL Fibrin Sealant (Human) Application Device.
Quantity: 738 devices (246 boxes of 3)
Why Was This Recalled?
Products labeled for distribution outside the United States may have been distributed to customers in the United States.
Where Was This Sold?
This product was distributed to 26 states: AL, AK, AZ, AR, CA, CO, FL, GA, IL, IA, MD, MI, MN, MO, NV, NJ, NY, NC, ND, OH, PA, TN, TX, WA, WV, WI
About Ethicon, Inc.
Ethicon, Inc. has 69 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report