Nonabsorbable suture anchor system intended to reattach recall
Nonabsorbable suture anchor system intended to reattach soft tissue to bone in orthopedic surgical procedures may be used in either arthroscopic or…
Why was Nonabsorbable suture anchor system intended to reattach recalled?
Manufactured with the incorrect anchor outer body
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 786351
- Product
- Nonabsorbable suture anchor system intended to reattach soft tissue to bone in orthopedic surgical procedures may be used in either arthroscopic or…
- Recalling firm
- ConMed Corporation
- Quantity
- 56 units
- Distribution
- CA, IN, KS, MD, NY, OH, PA, TN, TX & WI
- Recall date
- December 20, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)