Mckesson Medical-Surgical recalls 600mg sodium bicarbonate tablets due to temperature abuse risks. The recall affects 1000-count bottles from Major Pharma with NDC 0536-1047-10. No specific remedy is provided in the official notice.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling 600mg sodium bicarbonate tablets (1000-count bottles) made by Major Pharma. The recall is due to potential temperature abuse issues that could affect product safety. This recall does not include a specific remedy or timeline.
The product was manufactured under cGMP (current Good Manufacturing Practices) deviations related to temperature abuse. This means the tablets could be affected by improper storage or handling conditions, potentially compromising their safety and effectiveness.
Prescription patients who received the recalled tablets from Mckesson Medical-Surgical. Healthcare providers using these tablets for medical purposes may be at risk if temperature conditions are not properly managed.
Check for the 600mg sodium bicarbonate tablets in 1000-count bottles with NDC code 0536-1047-10. The product was distributed by Mckesson Medical-Surgical and may have been shipped to customers between the dates mentioned in the recall notice.
Identify if you have the 600mg sodium bicarbonate tablets in 1000-count bottles with NDC 0536-1047-10 from Mckesson Medical-Surgical.
The recall is due to cGMP deviations related to temperature abuse, which could affect product safety and effectiveness.
The official notice does not provide a specific remedy or action steps for affected customers.
The recall notice states that Mckesson Medical-Surgical cannot identify the particular lot number for each consignee, so lot numbers are not specified.
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-1058-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1058-2022 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.
