Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Smith&Nephew SmartStitch PerfectPasser Connector Recalled by ArthroCare Corporation Due to The voluntary recall is being initiated due to...
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 ArthroCare Corporation directly.
Affected Products
Smith&Nephew SmartStitch PerfectPasser Connector, REF # OM-8010, Rx Only, CE 0123, UDI: 00817470006971
Quantity: 15,559 units
Why Was This Recalled?
The voluntary recall is being initiated due to a manufacturing error resulting in incorrect upper jaw dimensions, and the upper jaw could potentially disengage or detach during use.
Where Was This Sold?
This product was distributed to 42 states: AL, AZ, AR, CA, CO, CT, FL, GA, HI, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NV, NH, NJ, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WV, WI
About ArthroCare Corporation
ArthroCare Corporation has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report