Mckesson Medical-Surgical recalls MethyLPREDNISolone Acetate Injectable Suspension (400 mg/10 mL) due to temperature abuse risks. This prescription-only product may be unsafe if exposed to improper temperatures.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical recalls a specific prescription injectable steroid product because it was manufactured under conditions that could lead to temperature abuse. This risk means the product might be unsafe if stored or handled incorrectly.
The product was made under cGMP (current Good Manufacturing Practice) deviations related to temperature abuse. This means the product could become unsafe if it's exposed to temperatures that aren't properly controlled, potentially leading to ineffective or harmful treatment.
Prescription patients who received this specific injectable steroid product from a pharmacy. Healthcare providers using this product in medical settings are at risk if they don't verify proper storage conditions.
Check for the product name 'MethyLPREDNISolone Acetate Injectable Suspension USP, 400 mg/10 mL (40 mg/mL), 10 mL multi-dose vial' on prescription labels. The product was distributed by Teva Pharma USA with NDC 0703-0045-01. McKesson Medical-Surgical cannot identify the specific lot numbers for each customer.
Look for the product name and NDC code 0703-0045-01 on the prescription label.
The recall states there were cGMP deviations related to temperature abuse, so the product may be unsafe if exposed to improper temperatures. The official notice does not specify if it's safe to use.
Check for the product name 'MethyLPREDNISolone Acetate Injectable Suspension USP, 400 mg/10 mL (40 mg/mL), 10 mL multi-dose vial' and NDC 0703-0045-01 on the prescription label.
The recall does not specify a remedy, so the official notice does not say what to do with the product.
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-1072-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1072-2022 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.
