Mckesson recalls 400mg ibuprofen tablets due to temperature abuse during storage. Products may be unsafe if exposed to high temperatures.
cGMP deviations: Temperature abuse
Mckesson is recalling 400mg ibuprofen tablets that may have been exposed to high temperatures. This could cause the medication to become unsafe for use.
The tablets may have been exposed to high temperatures during storage, which could cause the medication to become unsafe. This is a temperature abuse issue that affects the product's stability.
Prescription holders who received the specific product from Mckesson Medical-Surgical. People with chronic pain conditions using these tablets are most at risk.
Check for the product name 'Ibuprofen Tablets USP, 400 mg, 100-count unit dose box' with NDC 0904-5853-61. Products were distributed by Mckesson Medical-Surgical and may have been shipped to customers between the dates mentioned in the recall notice.
Look for the NDC code 0904-5853-61 on the product packaging.
The recall is due to temperature abuse during storage, which may make the medication unsafe.
Check for the NDC code 0904-5853-61 on the product packaging. The product was distributed by Mckesson Medical-Surgical.
The recall notice does not specify a remedy or action for the product.
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-1055-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1055-2022 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.
