Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Biosure Ratchet Driver Recalled by Smith & Nephew, Inc., Endoscopy Div. Due to Driver does not meet specification, oversized. Driver 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 Smith & Nephew, Inc., Endoscopy Div. directly.
Affected Products
Biosure Ratchet Driver, Product No: 72201888 For delivery and placement of orthopedic screws. Arthroscopic surgical instrument
Quantity: 9
Why Was This Recalled?
Driver does not meet specification, oversized. Driver may not be able to be fully inserted into the screw, or screw may become stuck on the driver.
Where Was This Sold?
This product was distributed to 17 states: AL, AK, CA, CO, FL, IL, IN, MI, NE, NJ, NY, OH, OK, PA, SC, TN, TX
About Smith & Nephew, Inc., Endoscopy Div.
Smith & Nephew, Inc., Endoscopy Div. has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report