Technocut Plus — Class II medical device recall Z-0891-2013
Terminated recall by Myco Medical Supplies Inc, reported 2013-03-06, distributed in CA, FL, IL, MI, MO, NY, OH, PA…. Pouch labeling/printing errors and defective packaging resulting in possible compromised sterility.
| Recall number | Z-0891-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Myco Medical Supplies Inc, Cary, NC, United States |
| Recall initiated | 2013-02-07 |
| Classified | 2013-02-27 |
| Reported by FDA | 2013-03-06 |
| Terminated | 2013-07-09 |
| Distributed | CA, FL, IL, MI, MO, NY, OH, PA, SC, TN, WI |
| Countries outside the US | CA |
| Quantity | 110,768 scalpels |
| Reason classes | labeling, sterility |
| Lot numbers | 1208224, 1208235, 1208276, 1208307, 1210105, 1210116, 1210189, 1211192, 1211213, 1211305, 1212041, 1212052 |
| Model numbers | 6008TR-10, 6008TR-11, 6008TR-12, 6008TR-15, 6008TR-20 |
Product
Technocut Plus, Sterile Single Use Safety Scalpel, Distributed by: Myco Medical.
Reason for recall
Pouch labeling/printing errors and defective packaging resulting in possible compromised sterility.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0891-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.