Mckesson Medical-Surgical recalls Vecuronium Bromide 10mg vials due to temperature abuse risks. Patients may face safety issues if the product is exposed to improper temperatures.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling Vecuronium Bromide for Injection vials because they may have been exposed to improper temperatures during storage or shipping. This could lead to safety risks for patients using the medication.
The medication may have been exposed to temperatures outside the recommended range during storage or shipping. This temperature abuse could affect the drug's safety and effectiveness.
Patients prescribed Vecuronium Bromide for Injection by a healthcare provider. Those who have received the specific product from Teva Pharma USA (NDC 0703-2914-03) are most at risk.
Check for the product name 'Vecuronium Bromide for Injection', 10 mg vials in 10-count boxes, manufactured by Teva Pharma USA (NDC 0703-2914-03). The recall covers products distributed by McKesson Medical-Surgical.
Identify if you have the specific product with NDC 0703-2914-03 from Teva Pharma USA.
The recall indicates potential temperature abuse risks, but the product may still be safe if stored properly. Consult your healthcare provider for guidance.
Check the product's NDC number (0703-2914-03) and manufacturer (Teva Pharma USA) to see if it matches the recalled items.
The recall does not specify a remedy, so contact your healthcare provider or pharmacy for advice on next steps.
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-1079-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1079-2022 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.
