Mckesson Medical-Surgical recalls E-Z-Gas II effervescent granules due to temperature abuse risks. Products may have been shipped with improper temperature control, potentially causing safety issues.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical recalls E-Z-Gas II effervescent granules that may have been exposed to improper temperatures during shipping. This could lead to safety risks if the product is used without proper temperature control.
The recall is due to cGMP deviations related to temperature abuse. This means the product may have been stored or shipped at temperatures that could compromise its safety and effectiveness.
Prescription patients who received E-Z-Gas II effervescent granules from Mckesson Medical-Surgical. Those who received the product after the distribution dates listed in the recall notice are most at risk.
Check for the product name 'E-Z-Gas II', net weight 4g, 50 packets per box, and NDC numbers 0270-9020-01 (discontinued) or 10361-793-01 (current). The product was distributed by Mckesson Medical-Surgical.
Identify the product by checking the NDC numbers 0270-9020-01 or 10361-793-01, and the net weight of 4g with 50 packets per box.
The product was recalled due to cGMP deviations related to temperature abuse, which may have compromised its safety and effectiveness.
Check for the product name 'E-Z-Gas II', net weight 4g, 50 packets per box, and NDC numbers 0270-9020-01 (discontinued) or 10361-793-01 (current).
The recall notice does not specify a remedy or action for the product. You should contact Mckesson Medical-Surgical for further instructions.
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-1085-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1085-2022 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.
