Mckesson Medical-Surgical recalls Gastrografin (Diatrizoate Meglumine and Diatrizoate Sodium Solution USP) due to temperature abuse risks. This prescription-only product may be unsafe if exposed to incorrect temperatures.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling Gastrografin (Diatrizoate Meglumine and Diatrizoate Sodium Solution USP) because of temperature abuse issues. This risk could lead to unsafe conditions if the product is exposed to incorrect temperatures.
The product was manufactured with cGMP deviations related to temperature abuse. This means the product could be unsafe if it is exposed to temperatures that are not properly controlled, potentially leading to incorrect dosing or safety issues.
Prescription patients who received Gastrografin from Mckesson Medical-Surgical. Healthcare providers using this product are most at risk due to potential temperature abuse.
Check for Gastrografin (Diatrizoate Meglumine and Diatrizoate Sodium Solution USP) in 24 single-dose 30 mL bottles. This product is prescription-only and manufactured by Bracco Diagnostics Inc. with NDC 0270-0445-35.
Look for the product name and packaging details to confirm if it matches the recalled items.
The recall indicates potential temperature abuse risks, so the product may not be safe if exposed to incorrect temperatures.
Check for Gastrografin (Diatrizoate Meglumine and Diatrizoate Sodium Solution USP) in 24 single-dose 30 mL bottles with NDC 0270-0445-35.
The recall does not specify a remedy, so contact your 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-1086-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1086-2022 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.
