Mckesson Medical-Surgical recalls MethyLPREDNISolone Acetate Injectable Suspension (200mg/5mL) 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 (200mg/5mL) because of temperature abuse risks. This prescription-only medication could become unsafe if stored or handled at incorrect temperatures.
The medication may be affected by improper temperature storage or handling, which could lead to reduced effectiveness or safety issues. Temperature abuse refers to exposure to temperatures that compromise the product's stability.
Prescription patients who received this specific injectable medication from a pharmacy. Those with the product in their possession are most at risk.
Look for the product name 'MethyLPREDNISolone Acetate Injectable Suspension, USP, 200mg/5mL (40 mg/mL), 5 mL multi-dose vial' with NDC 0703-0043-01. This prescription-only medication was distributed by McKesson Medical-Surgical.
Verify the product name and NDC code (0703-0043-01) to confirm if you have the recalled medication.
The recall indicates potential temperature abuse risks, but the product may still be safe if handled properly. Consult your healthcare provider for specific guidance.
Check for the product name 'MethyLPREDNISolone Acetate Injectable Suspension, USP, 200mg/5mL (40 mg/mL), 5 mL multi-dose vial' with NDC 0703-0043-01.
The recall does not specify a remedy, so contact your pharmacy or healthcare provider for advice 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-1071-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1071-2022 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.
