Mckesson Medical-Surgical recalls MethyLPREDNISolone Acetate Injectable Suspension (80 mg/mL) due to temperature abuse risks. Products were distributed with unclear lot numbers and may have been shipped at unsafe temperatures.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical recalls a specific injectable steroid product because it may have been exposed to unsafe temperatures during distribution. This could affect the product's safety and effectiveness if used improperly.
The product may have been exposed to unsafe temperatures during distribution, which can cause the medication to degrade. This degradation could lead to ineffective treatment or potential safety risks if the product is used without proper temperature control.
Prescription patients who received this specific injectable steroid product from a pharmacy. Healthcare providers using the product in clinical settings may also be affected.
Check for the product name 'MethyLPREDNISolone Acetate Injectable Suspension USP, 80 mg/mL' in a 1 mL single dose vial (NDC 0703-0051-01) or 25-count box (NDC 0703-0051-04). The product is prescription-only and distributed by Teva Pharma USA.
Verify the product name, strength, and NDC numbers to confirm if it matches the recalled items.
The recall is due to potential temperature abuse during distribution, which may cause the medication to degrade.
Look for the product name 'MethyLPREDNISolone Acetate Injectable Suspension USP, 80 mg/mL' in a 1 mL single dose vial (NDC 0703-0051-01) or 25-count box (NDC 0703-0051-04).
The official notice does not specify a remedy, so contact your pharmacy or healthcare provider 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-1073-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1073-2022 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.
