Mckesson Medical-Surgical recalls Pantoprazole Sodium 40mg vials due to temperature abuse risks. This affects prescription-only products from Sandoz Pharma with NDC 0781-3232-95.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical has recalled Pantoprazole Sodium for Injection vials because of temperature abuse risks. This could lead to unsafe drug conditions if stored improperly. Patients with prescriptions for this medication should check if they have the recalled product.
The recall is due to cGMP deviations related to temperature abuse. This means the medication could be exposed to temperatures that compromise its safety and effectiveness if not stored properly.
Prescription patients receiving Pantoprazole Sodium 40mg vials from Sandoz Pharma (NDC 0781-3232-95) are affected. Healthcare providers and pharmacies handling these products may also be impacted.
Check for vials labeled 'Pantoprazole Sodium for Injection, 40 mg/vial, 10 single-dose vials, Rx only' from Sandoz Pharma with NDC 0781-3232-95. The recall covers products distributed by McKesson Medical-Surgical.
Verify the product label includes 'Pantoprazole Sodium for Injection, 40 mg/vial, 10 single-dose vials, Rx only' and NDC 0781-3232-95.
The recall is due to cGMP deviations related to temperature abuse, which could compromise the medication's safety and effectiveness.
Check for vials labeled 'Pantoprazole Sodium for Injection, 40 mg/vial, 10 single-dose vials, Rx only' with NDC 0781-3232-95 from Sandoz Pharma.
The official notice does not specify a remedy for this recall, so contact your healthcare provider or pharmacy 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-1104-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1104-2022 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.
