Mckesson Medical-Surgical recalls Medroxyprogesterone acetate injectable vials due to temperature abuse risks. Affected products may have been shipped with improper temperature control.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling Medroxyprogesterone acetate injectable vials (150 mg/mL, 1 mL) because of temperature abuse issues. This could lead to unsafe drug concentrations if the product was exposed to incorrect temperatures during storage or transport.
The product may have been exposed to temperatures outside the required range during storage or shipping, leading to potential drug instability. This could result in unsafe concentrations of the medication if used.
Healthcare providers and patients who received the recalled vials for medical use. Those handling the product without proper temperature control are at higher risk.
Check for vials labeled 'Medroxyprogesterone acetate injectable suspension, USP, 150 mg/mL, 1 mL' with NDC numbers 0703-6801-01 (single dose) or 0703-6801-04 (25-count box). These are prescription-only products.
Look for NDC numbers 0703-6801-01 or 0703-6801-04 on the vial packaging.
Reach out to your healthcare provider to discuss whether the product was part of your prescription and if it needs to be discarded or replaced.
The product was recalled due to temperature abuse risks, meaning it may have been exposed to incorrect temperatures during storage or shipping, potentially affecting drug safety.
Check for vials labeled 'Medroxyprogesterone acetate injectable suspension, USP, 150 mg/mL, 1 mL' with NDC numbers 0703-6801-01 (single dose) or 0703-6801-04 (25-count box).
No immediate stop is required, but you should contact your healthcare provider to determine if the product was part of your prescription and if it needs to be discarded.
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-1069-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1069-2022 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.
