Mckesson Medical-Surgical recalls 25mg Meclizine tablets due to temperature abuse risks. Affected products were distributed without clear lot numbers for prescription use.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling 25mg Mecl: 50-count tablets that may have been exposed to improper temperatures. This could affect the medication's safety and effectiveness.
Temperature abuse means the medication may have been stored or handled at unsafe temperatures, potentially affecting its safety and effectiveness. This could lead to improper medication response or harm.
Prescription patients who received Meclizine tablets from Mckesson Medical-Surgical. Those with specific prescription orders are most at risk.
Check for Meclizine Hydrochloride Tablets, 25mg, 50-count cartons with NDC 50268-523-15. Products were distributed to customers with specific dates but lot numbers were not identified by Mckesson.
Look for the NDC code 50268-523-15 on the packaging to confirm if your tablets are affected.
The recall is due to temperature abuse risks that may affect the medication's safety and effectiveness.
The official notice does not specify a stop-use instruction, so you should check product details before taking.
Mckesson Medical-Surgical cannot identify the particular lot number for each consignee, so check the NDC code on packaging.
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-1037-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1037-2022 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.
