Technocut Plus recall: Sterility Concern
Technocut Plus, Sterile Single Use Safety Scalpel, Distributed by: Myco Medical.
Why was Technocut Plus recalled?
Pouch labeling/printing errors and defective packaging resulting in possible compromised sterility.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
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.
- Product
- Technocut Plus, Sterile Single Use Safety Scalpel, Distributed by: Myco Medical.
- Recalling firm
- Myco Medical Supplies Inc
- Quantity
- 110,768 scalpels in individual pouches
- Distribution
- Worldwide Distribution - USA including CA, FL, IL, MI, MO, NY, OH, PA, SC, TN, WI and Internationally to Canada
- Recall date
- March 6, 2013
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)