Surgicutt fully automated incision making device for recall
Surgicutt fully automated incision making device for bleeding time determination. ITC 8 Olsen Avenue, Edison, NJ 08820. 732.548.5700. www.itcmed.com.…
Why was Surgicutt fully automated incision making device for recalled?
ITC has determined that the blade in their Surgicutt with Blotting Paper (Product Code: SUB50I; Lot: AK301M) devices may be loose.
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?
Product Code: SUB50I; Lot No. AK301M. Lot Expiration Date 8/31/2017
- Product
- Surgicutt fully automated incision making device for bleeding time determination. ITC 8 Olsen Avenue, Edison, NJ 08820. 732.548.5700. www.itcmed.com.…
- Recalling firm
- ITC-Nexus Dx
- Quantity
- 6 boxes (Each box contains 50 Surgicutt Devices plus 55 sheets of Blotting Paper).
- Distribution
- Nationwide Distribution including Arizona andTexas. .
- Recall date
- November 13, 2013
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)