Mckesson Medical-Surgical recalls MethyLPREDN: 40 mg/mL injectable suspension due to temperature abuse risks. Product may have been shipped with improper storage conditions.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling MethyLPREDNISolone Acetate Injectable Suspension (40 mg/mL) because of temperature abuse risks. This could lead to unsafe drug conditions if stored improperly.
The product was manufactured with temperature abuse risks, meaning it could be stored or handled in ways that compromise its safety. This could lead to unsafe drug conditions if not stored properly.
Prescription patients using MethyLPREDNISolone Acetate Injectable Suspension (40 mg/mL) from Mckesson Medical-Surgical. Patients who received this product in a 1 mL vial or 25-count box are most at risk.
Check for the product name 'MethyLPREDNISolone Acetate Injectable Suspension, USP, 40 mg/mL' in a 1 mL single dose vial (NDC 0703-0031-01) or 25-count box (NDC 0703-0031-04). This product is prescription-only and distributed by Mckesson Medical-Surgical.
Identify the product by checking the NDC numbers: 0703-0031-01 for the 1 mL vial or 0703-0031-04 for the 25-count box.
The product was recalled due to temperature abuse risks, which could lead to unsafe drug conditions if stored improperly.
Check for the product name 'MethyLPREDNISolone Acetate Injectable Suspension, USP, 40 mg/mL' in a 1 mL single dose vial (NDC 0703-0031-01) or 25-count box (NDC 0703-0031-04).
The recall does not specify a remedy, so contact your healthcare provider for guidance on safe handling or disposal.
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-1070-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1070-2022 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.
