Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Miocol-E (acetylcholine chloride intraocular solution) 20 mg/2mL (10 mg/mL) Recalled by Mckesson Medical-Surgical Inc. Corporate Office Due to cGMP deviations: Temperature abuse
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 Mckesson Medical-Surgical Inc. Corporate Office directly.
Affected Products
Miocol-E (acetylcholine chloride intraocular solution) 20 mg/2mL (10 mg/mL), Rx only, Manufacturer: Bausch & Lomb, NDC 24208-539-20
Quantity: 45 kits
Why Was This Recalled?
cGMP deviations: Temperature abuse
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Mckesson Medical-Surgical Inc. Corporate Office
Mckesson Medical-Surgical Inc. Corporate Office has 276 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report