Mckesson Medical-Surgical recalls Aparaclonidine Ophthalmic Solution 0.5% 5mL bottles (NDC 61314-665-05) due to temperature abuse risks. The recall follows cGMP deviations in manufacturing.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling Aparaclonidine Ophthalmic Solution 0.5% 5mL bottles (NDC 61314-665-05) because of temperature abuse risks during manufacturing. This could lead to unsafe drug conditions if the product is exposed to improper temperatures.
The product was manufactured with cGMP deviations related to temperature abuse. This means the medication could be unstable or ineffective if exposed to temperatures outside the recommended range, potentially leading to unsafe conditions.
Prescription holders of Aparaclonidine Ophthalmic Solution 0.5% 5mL bottles (NDC 61314-665-05) from Mckesson Medical-Surgical. Patients using this medication are most at risk if the product was exposed to improper temperatures.
Check for the product name 'Aparaclonidine Ophthalmic Solution 0.5% 5mL bottle' with NDC 61314-665-05. The recall covers prescription products distributed by Mckesson Medical-Surgical.
Identify the product by checking the NDC code 61314-665-05 and the prescription label.
The recall indicates potential temperature abuse risks, but the official notice does not specify if the product is safe to use.
Check the NDC code 61314-665-05 on the product label to confirm it is part of this recall.
The official notice does not specify a remedy, so contact Mckesson Medical-Surgical for guidance.
We’ve drafted a message you can send Mckesson Medical-Surgical to request your refund or repair — edit it as you like.
Subject: Recall D-1026-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1026-2022 from Mckesson Medical-Surgical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
