FDA Device recall Z-0891-2013
Technocut Plus, Sterile Single Use Safety Scalpel, Distributed by: Myco Medical
- FDA Device
- Class II
- terminated
- Published 2013-03-06
On 2013-03-06 the FDA classified a Class II recall of Technocut Plus, Sterile Single Use Safety Scalpel, Distributed by: Myco Medical by Myco Medical Supplies, citing pouch labeling/printing errors and defective packaging resulting in possible compromised sterility.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0891-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-02-07 |
| Published | 2013-03-06 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Myco Medical Supplies |
| Distribution | CA, FL, IL, MI, MO, NY, OH, PA, SC, TN, WI |
Product
Technocut Plus, Sterile Single Use Safety Scalpel, Distributed by: Myco Medical.
Reason
Pouch labeling/printing errors and defective packaging resulting in possible compromised sterility.
Identifiers
| code_info | Catalogue number: 6008TR-10, 6008TR-11, 6008TR-12, 6008TR-15, 6008TR-20; Batch numbers: 1208235, 1210189, 1211305, 1208…Catalogue number: 6008TR-10, 6008TR-11, 6008TR-12, 6008TR-15, 6008TR-20; Batch numbers: 1208235, 1210189, 1211305, 1208276, 1211213, 1208224, 1210105, 1212041, 1208307, 1211192, 1212052, 1210116. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0891-2013%22
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