Mckesson Medical-Surgical recalls 100mg Doxycycline Capsules due to temperature abuse risks. This affects prescription products distributed by Sun Pharmaceuticals with NDC 63304-616-50.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling 100mg Doxycycline Capsules that may have been exposed to improper temperatures. This could affect the medication's safety and effectiveness for patients using prescription-only products.
Temperature abuse refers to the product being exposed to temperatures outside the recommended range during storage or transport. This could compromise the medication's stability and effectiveness, potentially leading to unsafe use.
Prescription holders of Doxycycline Capsules (100mg, 50-count) distributed by Sun Pharmaceuticals. Patients using these medications are most at risk if the product was exposed to improper temperatures.
Check for the product name 'Doxycycline Capsules, USP, 100 mg, 50-count bottle' with NDC 63304-616-50. The product was distributed by Sun Pharmaceuticals and is prescription-only.
Verify the product name and NDC code to confirm if it matches the recalled items.
The recall indicates potential temperature abuse, which could affect safety and effectiveness. Consult your healthcare provider for specific guidance.
Check for Doxycycline Capsules, USP, 100 mg, 50-count bottle with NDC 63304-616-50 distributed by Sun Pharmaceuticals.
The recall does not specify a remedy, so contact your healthcare provider for advice on safe handling.
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-1032-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1032-2022 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.
