Artholine Punch B 4 recall
Artholine Punch B 4, 6MM H 1, 6MM, used for the removal of soft tissue, cartilage tissue or other non-osseous tissue via natural or surgically created…
Why was Artholine Punch B 4 recalled?
Punch may have a burr in one section of the joint and when the punch is open, there is an increase potential for injury.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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 Number 89140.0105, Lot Number 4500197481
- Product
- Artholine Punch B 4, 6MM H 1, 6MM, used for the removal of soft tissue, cartilage tissue or other non-osseous tissue via natural or surgically created…
- Recalling firm
- Richard Wolf GmbH
- Quantity
- 12 units
- Distribution
- Worldwide distribution to Germany, Hong Kong, Ireland, Romania, and Turkey.
- Recall date
- August 29, 2018
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)