WECK Visistat 35R Disposable Skin Stapler recall
WECK Visistat 35R Disposable Skin Stapler, Ref 528135, Rx Only, Sterile EO, Visistat is indicated for the external skin closure of lacerations on the…
Why was WECK Visistat 35R Disposable Skin Stapler recalled?
Some boxes are labeled as containing Visistat Wide devices, when they in fact they contained Visistat Regular device.
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?
73H1600207
- Product
- WECK Visistat 35R Disposable Skin Stapler, Ref 528135, Rx Only, Sterile EO, Visistat is indicated for the external skin closure of lacerations on the…
- Recalling firm
- Teleflex Medical
- Quantity
- 3594 eaches
- Distribution
- Worldwide Distribution - US including CA, FL, GA, IL, IN, KS, KY, ME, MD, MA, MI, NJ, NY, NC, OH, OR, RI, TX, UT, VA, and Internationally to Australia, Belgium and France
- Recall date
- May 24, 2017
- Classification
- Class II
- Status
- Completed
- Agency
- FDA (device)