Weck Facial Closure Systems have application in recall
Weck Facial Closure Systems have application in laparoscopic procedures for approximation of tissues and percutaneous suturing for closing incision…
Why was Weck Facial Closure Systems have application in recalled?
The devices wings may become partially detached from the EFx Shield during use.
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: EFX002, Lot numbers: 3264480000, 3269990000, 3270100000.
- Product
- Weck Facial Closure Systems have application in laparoscopic procedures for approximation of tissues and percutaneous suturing for closing incision…
- Recalling firm
- Teleflex Medical
- Quantity
- 2265 units
- Distribution
- Domestic; US Nationwide; International: Belgium, Canada.
- Recall date
- December 21, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)