Mckesson Medical-Surgical recalls MethyLPREDNISolone Acetate Injectable Suspension (400 mg/10 mL) due to temperature abuse risks. This prescription-only product may be unsafe if exposed to improper temperatures.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling MethyLPREDNISolone Acetate Injectable Suspension (400 mg/10 mL) because of temperature abuse risks. This prescription-only medication could be unsafe if stored or handled at incorrect temperatures.
The product was manufactured under cGMP deviations related to temperature abuse. This means the medication could be unstable or ineffective if exposed to temperatures outside the recommended range, potentially leading to safety issues.
Prescription patients who received this specific injectable medication from a pharmacy. Healthcare providers using this product in medical settings may be at risk if temperature controls are inadequate.
Check for the product name 'MethyLPREDNISolone Acetate Injectable Suspension, USP, 400 mg/10 mL (40 mg/mL), 10 mL Multiple Dose Vial' with NDC 16714-090-01. This prescription-only medication was distributed by McKesson Medical-Surgical.
Verify the product name and NDC code (16714-090-01) to confirm if you have the recalled medication.
The recall indicates potential temperature abuse risks, but the official notice does not specify if the medication is safe to use without proper temperature control.
The recall notice does not mention any replacement options or remedies for affected products.
The product was recalled due to cGMP deviations related to temperature abuse, meaning it may be unsafe if exposed to improper temperatures.
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-1063-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1063-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
