Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Healon GV PRO 0.85 mL Recalled by Johnson & Johnson Surgical Vision Inc Due to Ophthalmic viscosurgical device may be difficult to remove...
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 Johnson & Johnson Surgical Vision Inc directly.
Affected Products
Healon GV PRO 0.85 mL, Model (U.S.): 10-2400-14, Model (O.U.S.): 10-2705-14, 10-2715-14, 10-2725-14, and 10-2755-14
Quantity: N/A
Why Was This Recalled?
Ophthalmic viscosurgical device may be difficult to remove from the eye, leading to increased postoperative intraocular pressure requiring additional intervention. Also, reports of clogging of phacoemulsion equipment tubing, which may lead to delay in the procedure or ocular injury.
Where Was This Sold?
This product was distributed to 46 states: AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, IA, 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, VT, VA, WA, WV, WI, DC
About Johnson & Johnson Surgical Vision Inc
Johnson & Johnson Surgical Vision Inc 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