Mckesson Medical-Surgical recalls DermaCol 100 Collagen Powder (Model 00300E) due to potential temperature exposure during shipping from June 2021-August 2021. This may reduce product effectiveness but is unlikely to cause health issues.
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21. This device with this specific storage temperature deviation is not likely to cause adverse health consequences.
Mckesson Medical-Surgical is recalling DermaCol 100 Collagen Powder (Model 00300E) because it may have been exposed to higher temperatures during shipping from June to August 2021. This could reduce the product's effectiveness but is not expected to cause health problems.
The product may have been exposed to higher temperatures during shipping from June 2021 to August 2021. This temperature deviation could reduce the product's effectiveness but is unlikely to cause health problems.
Users of DermaCol 100 Collagen Powder (Model 00300E) purchased between June 1, 2021 and September 30, 2021. People using this product for medical purposes may be affected if it was exposed to higher temperatures during shipping.
Check for the model number 00300E on the DermaCol 100 Collagen Powder packaging. The product was sold between June 1, 2021 and September 30, 2021.
Look for the model number 00300E on the DermaCol 100 Collagen Powder packaging.
No, the recall states this device with temperature deviations is unlikely to cause adverse health consequences.
The recall covers products received between June 1, 2021 and September 30, 2021.
The recall does not specify a remedy, so no action is required beyond checking if you have the affected 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 Z-1789-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall Z-1789-2022 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.
