Mckesson Medical-Surgical recalls Lidocaine 5% patches due to temperature abuse during storage. This may cause product failure. Check your prescription box for NDC 0591-3525-30.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical recalls Lidocaine 5% patches (30-count) because they may have been exposed to improper temperatures during storage. This could lead to product failure, but the recall does not specify immediate safety risks.
The patches may have been exposed to temperatures outside the recommended range during storage. This could cause the medication to become ineffective or degrade, but the recall does not indicate a risk of injury or serious harm.
Prescription holders with the specific NDC 0591-3525-30 box. Patients using the patches for pain relief are most at risk if the product was stored incorrectly.
Check your prescription box for the NDC code 0591-3525-30. The product is a 30-count Lidocaine 5% patch, available by prescription only.
Look for the NDC code 0591-3525-30 on the box to confirm if your product is affected.
The recall does not indicate that the product is dangerous when used correctly. The issue is related to storage conditions.
The official notice does not specify a remedy for this recall. You should check the product details to see if it matches the NDC code 0591-3525-30.
The recall does not state that the product is unsafe for use. However, if the product was stored incorrectly, it may not work as intended.
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-1068-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1068-2022 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.