Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Nordson Micromedics FibriJet Endoscopic Catheter Introducer Recalled by Micromedics, Inc. Due to The sterile packaging may contain small channels in...
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 Micromedics, Inc. directly.
Affected Products
Nordson Micromedics FibriJet Endoscopic Catheter Introducer, Catalog Number SA-3445. Sterilized using Ethylene Oxide
Quantity: 273 units
Why Was This Recalled?
The sterile packaging may contain small channels in the seal of the pouch, If the channels are present, the package integrity may be compromised which may affect sterility assurance.
Where Was This Sold?
This product was distributed to 9 states: AL, CA, FL, MS, NJ, NY, NC, TN, TX
About Micromedics, Inc.
Micromedics, Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report