Mckesson Medical-Surgical recalls Geodon 20 mg/mL 1mL vials due to temperature abuse risks. Affected products may have been shipped without proper temperature control.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical recalls Geodon injection vials that may have been improperly stored. This could lead to unsafe drug conditions if the vials were exposed to incorrect temperatures.
The vials may have been exposed to temperatures outside the required range during shipping or storage. This temperature abuse could cause the medication to become unstable or ineffective, potentially leading to unsafe drug conditions.
Prescription patients using Geodon injections from pharmacies that received the recalled vials. Healthcare providers handling these vials may be at risk if they were stored incorrectly.
Check for Geodon 20 mg/mL 1mL single-dose vials with NDC 0049-3920-83. The recall affects vials distributed by Mckesson Medical-Surgical that may have been shipped without proper temperature control.
Identify the product by checking the NDC code 0049-3920-83 and the vial size (1 mL single-dose).
The recall is due to potential temperature abuse during shipping or storage, which could affect the medication's safety and effectiveness.
The official notice does not specify a remedy for this recall. Check with your pharmacy for guidance.
Look for Geodon 20 mg/mL 1mL single-dose vials with NDC 0049-3920-83. The recall affects vials distributed by Mckesson Medical-Surgical that may have been shipped without proper temperature control.
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-1112-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1112-2022 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.
