Mckesson Medical-Surgical recalls Xylocaine + Epinephrine 1% multi-dose vials due to temperature abuse risks. Products may have been shipped without proper temperature control, potentially causing safety issues.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling Xylocaine + Epinephrine 1% multi-dose vials that may have been exposed to improper temperatures. This could lead to unsafe drug conditions if the vials are used without proper temperature control.
The vials may have been exposed to temperatures outside the required range during shipping or storage. This temperature abuse could compromise the drug's safety and effectiveness, potentially leading to adverse effects if used improperly.
Healthcare professionals and patients who have prescription Xylocaine + Epinephrine 1% vials with NDC 63323-482-27 or 63323-482-57 are affected. Those who received these vials from McKesson Medical-Surgical may be at risk.
Check for vials labeled with NDC 63323-482-27 (20 mL, 25-count) or NDC 63323-482-57 (50 mL, 25-count). These are prescription-only products sold by McKesson Medical-Surgical.
Look for the National Drug Code (NDC) numbers 63323-482-27 or 63323-482-57 on the vial packaging.
The recall is due to potential temperature abuse during shipping or storage, which could compromise the drug's safety and effectiveness.
Check for vials with NDC numbers 63323-482-27 (20 mL, 25-count) or 63323-482-57 (50 mL, 25-count).
The official recall notice does not specify a remedy or action steps beyond checking the product labels.
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-1052-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1052-2022 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.
