Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
American Catheter / Cholangiogram Catheter 9100 Series. Recalled by American Catheter Corp Due to Catheters were not sealed before sterilization. and was...
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 American Catheter Corp directly.
Affected Products
American Catheter / Cholangiogram Catheter 9100 Series.
Quantity: 890 devices.
Why Was This Recalled?
Catheters were not sealed before sterilization. and was not detected through subsequent acceptance activities, product release and distribution.
Where Was This Sold?
This product was distributed to 21 states: AL, AK, CA, CO, FL, GA, HI, IL, KS, LA, MI, MO, MT, NJ, OH, OK, SC, TN, TX, WA, WI
About American Catheter Corp
American Catheter Corp 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