Mckesson Medical-Surgical recalls 50mg Metoprolol tablets due to temperature abuse risks. Consumers should check product details and contact pharmacy for guidance.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical recalls 50mg Metoprolol 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 temperatures that could compromise its safety. This could lead to ineffective or harmful medication.
Prescription holders of Metoprolol 50mg tablets from Sun Pharmaceuticals (NDC 57664-0477-52) are affected. Those with the product may be at risk if it was stored improperly.
Check for the product name 'Metoprolol tablets 50 mg, 100-count', manufacturer 'Sun Pharmaceuticals', and NDC code 57664-0477-52. The recall covers prescription products distributed by Mckesson Medical-Surgical.
Identify the product by checking the label for 'Metoprolol tablets 50 mg, 100-count', manufacturer 'Sun Pharmaceuticals', and NDC 57664-0477-52.
The recall is due to temperature abuse risks that could compromise the medication's safety and effectiveness.
Check the label for 'Metoprolol tablets 50 mg, 100-count', manufacturer 'Sun Pharmaceuticals', and NDC 57664-0477-52.
The recall does not specify a remedy, so contact your pharmacy 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-1110-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1110-2022 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.
