Ace Surgical Supply recalls Double Blade Shoe F/Unigraft Knife 1.5 Thick X 9MM SKU 6500009 due to incorrect packaging. A single blade shoe was mistakenly included instead of a double blade.
The product inside the package is incorrect. A single blade shoe was mistakenly packaged instead of a double blade.
Ace Surgical Supply is recalling a specific surgical knife model because it was incorrectly packaged with a single blade instead of the required double blade. This could lead to improper surgical procedures if used without the correct blade configuration.
The product was mistakenly packaged with a single blade shoe instead of the double blade. Using this incorrect blade could result in improper surgical outcomes during epithelial graft procedures in the oral cavity.
Surgical professionals and dental practitioners who use this knife for oral cavity epithelial grafts. Those who received the product with a single blade instead of double blade are most at risk.
Check for the product name 'Double Blade Shoe F/Unigraft Knife 1.5 Thick X 9MM SKU 6500009' and lot number M050225. The product is used for oral cavity epithelial grafts.
Verify the product has a double blade by checking the packaging for the correct SKU 6500009 and lot number M050225.
The product was recalled because a single blade shoe was mistakenly packaged instead of a double blade.
The correct product is a Double Blade Shoe F/Unigraft Knife 1.5 Thick X 9MM SKU 6500009.
Check for the product name 'Double Blade Shoe F/Unigraft Knife 1.5 Thick X 9MM SKU 6500009' and lot number M050225.
We’ve drafted a message you can send Ace Surgical Supply to request your refund or repair — edit it as you like.
Subject: Recall Z-1464-2018 — Ace Surgical Supply Ace Surgical Supply Hello, I own a Ace Surgical Supply that is covered by recall Z-1464-2018 from Ace Surgical Supply. 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.
