Mckesson recalls Xylocaine MPF (lidocaine HCl and epinephrine injection) 1% 300mg/30mL single-dose vials due to temperature abuse risks. Prescription-only products with NDC 63323-0487-31 may be affected.
cGMP deviations: Temperature abuse
Mckesson is recalling Xylocaine MPF injection vials because of temperature abuse risks. This could lead to unsafe drug conditions if the product is exposed to improper temperatures during storage or transport.
The recall is for temperature abuse risks, meaning the product could be improperly stored or transported, potentially leading to unsafe drug conditions. This is a cGMP (current Good Manufacturing Practice) deviation that affects product safety.
Prescription patients using Xylocaine MPF 1% 300mg/30mL vials from Mckesson Medical-Surgical. Healthcare providers handling these products may be at risk if temperature conditions are not properly managed.
Check for Xylocaine MPF (lidocaine HCl and epinephrine injection, USP) 1% 300mg/30mL single-dose vials in 5-count boxes with NDC 63323-0487-31. These are prescription-only products distributed by Mckesson Medical-Surgical.
Verify the product's NDC number (63323-0487-31) and that it's a 5-count box of Xylocaine MPF 1% 300mg/30mL vials.
The product was recalled due to cGMP deviations related to temperature abuse risks, which could lead to unsafe drug conditions.
Check for Xylocaine MPF 1% 300mg/30mL single-dose vials in 5-count boxes with NDC 63323-0487-31, which are prescription-only products distributed by Mckesson Medical-Surgical.
The recall record does not specify a remedy, so contact Mckesson Medical-Surgical for guidance 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-1050-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1050-2022 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.
