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.
“Ace Surgical Double Blade Shoe Knife Recall: Incorrect Package Contents.” GovInfoNow, updated August 21, 2026. https://govinfonow.com/recall/71594-ace-surgical-double-blade-shoe-knife-recall-incorrect-package-contents. Based on FDA recall #Z-1464-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1464-2018%22&limit=1).
The FDA announced on 2018-03-28 that Ace Surgical Supply Co., Inc. voluntarily recalled Double Blade Shoe F/Unigraft Knife units due to incorrect product packaging, according to the FDA.
The product inside the package is incorrect, as a single blade shoe was mistakenly packaged instead of a double blade, according to the FDA.
Context
GovInfoNow's records show Ace Surgical Supply Co., Inc. has two other recalls on record since 2017-10-24. Other recent recalls of similar products include Kii Low Profile Bladed Dual Pack Recall (2025-12-11), Encore Medical EMPOWR Acetabular System Recall (2026-01-05), and Encore Medical EMPOWR 3D KNEE Ins 11L 14MM VE: Packaging Mix-Up Recall (2026-02-16).
How to tell if you have this one
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.
Brand
Ace Surgical Supply
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Details
Verify the product has a double blade by checking the packaging for the correct SKU 6500009 and lot number M050225.
Where it went and when
Where it was distributed
Distributed in 3 states, and outside the U.S.
Listed by the agency
Not listed
FDA distribution: “US Distribution to the states of : MI, CA, OK, and Internationally to China, Canada,” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Michigan, Oklahoma.
Recall timeline
FDA terminated this recall 5 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-1464-2018 (March 28, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1464-2018 to see it in context.
Plain-language summary written by qwen3:4b on August 21, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.