Mckesson Medical-Surgical recalls Pilocarpine HCL Ophthalmic Solution 2% 15mL (Rx only) due to temperature abuse risks. Affected products have NDC 7006919101 from Somerset Therapeutics.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling Pilocarpine HCL Ophthalmic Solution 2% 15mL (Rx only) because of temperature abuse risks. This could lead to unsafe medication 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 compromised if stored or handled at temperatures outside the recommended range, potentially affecting its safety and effectiveness.
Prescription patients who received this specific medication from a pharmacy. Patients using the product without proper temperature control are at risk.
Check for the NDC code 7006919101 on the product label. The product is a prescription medication (Rx only) with a 15mL size and 2% concentration of Pilocarpine HCL.
Look for the NDC code 7006919101 on the product label to confirm if it is affected.
The recall indicates potential temperature abuse risks, so it is not safe to use without verifying the product's condition.
Check for the NDC code 7006919101 on the product label. This product is a prescription medication (Rx only) with a 15mL size and 2% concentration of Pilocarpine HCL.
The recall does not specify a remedy, so contact your pharmacy or healthcare provider 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-1109-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1109-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.