Mckesson Medical-Surgical recalls MethyLPREDNISolone Acetate Injectable Suspension (40 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 medication because it may have been exposed to unsafe temperatures during distribution. This could affect the medication's safety and effectiveness.
The medication may have been exposed to unsafe temperatures during distribution, which could lead to improper stability or effectiveness. Temperature abuse risks are not clearly defined in the recall notice.
Prescription patients who received this specific injectable steroid medication. Healthcare providers who dispensed the product may also be affected.
Check for the product name 'MethyLPREDNISolone Acetate Injectable Suspension USP, 40 mg/mL' in single-dose vials (NDC 6714-088-01) or 25-count boxes (NDC 16714-088-25). The product is prescription-only and distributed by McKesson Medical-Surgical.
Identify the product by checking the NDC codes: 6714-088-01 for single-dose vials or 16714-088-25 for 25-count boxes.
The recall is due to potential temperature abuse during distribution, which may affect the medication's safety and effectiveness.
Check for the product name 'MethyLPREDNISolone Acetate Injectable Suspension USP, 40 mg/mL' in single-dose vials (NDC 6714-088-01) or 25-count boxes (NDC 16714-088-25).
The recall notice does not specify a remedy or action for affected products.
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-1061-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1061-2022 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.
