FDA Device recall Z-1464-2018
Double Blade Shoe F/Unigraft Knife 1.5 Thick X 9MM SKU 6500009 Used to achieve epithelial graft in the oral cavity
- FDA Device
- Class II
- terminated
- Published 2018-05-02
On 2018-05-02 the FDA classified a Class II recall of Double Blade Shoe F/Unigraft Knife 1.5 Thick X 9MM SKU 6500009 Used to achieve epithelial graft in the oral cavity by Ace Surgical Supply, citing the product inside the package is incorrect. A single blade shoe was mistakenly packaged instead of a double blade.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1464-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-03-28 |
| Published | 2018-05-02 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ace Surgical Supply |
| Distribution | CA, MI, OK |
Product
Double Blade Shoe F/Unigraft Knife 1.5 Thick X 9MM SKU 6500009 Used to achieve epithelial graft in the oral cavity.
Reason
The product inside the package is incorrect. A single blade shoe was mistakenly packaged instead of a double blade.
Identifiers
| code_info | Lot # M050225 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Other recalls by Ace Surgical Supply
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FDA Drug · Class II · 2017-11-15 · Ace Surgical Supply - INFINITY Internal Hex Healing Abutment, 4.5mm Platform, 4.7mm CW-3mm CH Straight
FDA Device · Class II · 2017-04-26 · Ace Surgical Supply
All Ace Surgical Supply recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1464-2018%22
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