Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Bausch + Lomb Stellaris Elite 23 GA Vit Cutter Recalled by Bausch & Lomb Inc Due to The back cap separates from the body of...
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 Bausch & Lomb Inc directly.
Affected Products
Bausch + Lomb Stellaris Elite 23 GA Vit Cutter, Model BL5627, 7500 cpm, packaged in sterile pouches, 6/shipper.
Quantity: 103.33 cases
Why Was This Recalled?
The back cap separates from the body of the vitrectomy cutter.
Where Was This Sold?
This product was distributed to 26 states: AL, AZ, CA, CO, FL, GA, HI, IL, IN, KS, KY, ME, MA, MO, MT, NJ, NY, NC, OH, OK, OR, PA, TN, TX, UT, WV
About Bausch & Lomb Inc
Bausch & Lomb Inc has 17 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report