Mckesson Medical-Surgical recalls MethyLPREDNISolone Acetate Injectable Suspension 400mg/5mL vials due to temperature abuse risks. This prescription-only product may be unsafe if exposed to improper temperatures.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical has recalled MethyLPREDNISolone Acetate Injectable Suspension vials because of temperature abuse risks. This means the medication could be unsafe if stored or handled at incorrect temperatures, potentially causing harm to patients.
The medication may be affected by temperature abuse, meaning it could become unsafe if stored or handled at incorrect temperatures. This risk is specific to the injectable form and requires proper temperature control to maintain safety.
Prescription patients using MethyLPREDNISolone Acetate Injectable Suspension 400mg/5mL vials from Teva Pharma. Healthcare providers who dispensed these vials are most at risk of handling compromised products.
Look for vials labeled 'MethyLPREDNISolone Acetate Injectable Suspension USP, 400 mg/5mL (80 mg/mL), 5 mL multi-dose' from Teva Pharma. These are prescription-only products with NDC 0703-0063-01.
Verify the product label for the specific NDC 0703-0063-01 vial to confirm it is part of the recall.
The recall is due to cGMP deviations related to temperature abuse, which could make the medication unsafe if stored or handled at incorrect temperatures.
Check the product label for NDC 0703-0063-01. If you have the recalled vials, contact your healthcare provider for guidance on safe handling or disposal.
The official recall notice does not specify a deadline for action, but you should check the product label and contact your healthcare provider immediately.
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-1074-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1074-2022 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.
