Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Direct Drive Clip Applier CA090 Recalled by Applied Medical Resources Corp Due to Increased customer complaints indicating inconsistent clip application; may...
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 Applied Medical Resources Corp directly.
Affected Products
Direct Drive Clip Applier CA090, indicated for ligation of tubular structures or vessels in laparoscopic and general surgical procedures. Distributed individually and in kits.
Quantity: 559,274
Why Was This Recalled?
Increased customer complaints indicating inconsistent clip application; may lead to unoccluded vessels.
Where Was This Sold?
This product was distributed to 43 states: AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, ID, IL, IN, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NH, NJ, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WY, DC
About Applied Medical Resources Corp
Applied Medical Resources Corp has 30 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report