Teleflex MEDICAL WECK Visistat 35. Used for the recall
Teleflex MEDICAL WECK Visistat 35. Used for the external skin closure of lacerations.
Why was Teleflex MEDICAL WECK Visistat 35. Used for the recalled?
Some boxes are labeled as Visistat Wide devices, when in fact the contain Visistat Regular devices. The 6 individually packaged units within the boxes are correctly labeled.
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?
Lot Number 73H1600207
- Product
- Teleflex MEDICAL WECK Visistat 35. Used for the external skin closure of lacerations.
- Recalling firm
- Teleflex Medical
- Quantity
- 12 units
- Distribution
- KS
- Recall date
- April 4, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)