Mckesson Medical-Surgical recalls MethyLPREDNISolone Acetate Injectable Suspension for temperature abuse risks. This prescription-only product may be unsafe if exposed to improper temperatures.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical has recalled a specific prescription injection product due to temperature abuse risks. This means the medication could be unsafe if stored or handled at incorrect temperatures.
The product was manufactured under cGMP (current Good Manufacturing Practice) deviations related to temperature abuse. This means the medication could become unsafe if exposed to temperatures outside the recommended range, potentially leading to ineffective or harmful treatment.
Prescription patients who received this specific injection 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, 200 mg/5 mL (40 mg/mL), 5 mL Multiple Dose Vial' with NDC 16714-089-01. This prescription-only product was distributed by McKesson Medical-Surgical.
Identify the product by its name, NDC code 16714-089-01, and prescription status.
The product was manufactured under cGMP deviations related to temperature abuse, which could make it unsafe if exposed to improper temperatures.
Look for the product name 'MethyLPREDNISolone Acetate Injectable Suspension, USP, 200 mg/5 mL (40 mg/mL), 5 mL Multiple Dose Vial' with NDC 16714-089-01.
The recall 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-1062-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1062-2022 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.
