Compress Device Short Anchor Plug recall
Compress Device Short Anchor Plug, 26 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item…
Why was Compress Device Short Anchor Plug recalled?
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
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?
Lot Numbers/UDI: 535450 (01)00880304461611(17)270727(10)535450; 577600 (01)00880304461611(17)270630(10)577600; 577610 (01)00880304461611(17)270702(10)577610; 577760 (01)00880304461611(17)270629(10)577760; 671540 (01)00880304461611(17)271124(10)671540; 671890 (01)00880304461611(17)271114(10)671890; 671890R (01)00880304461611(17)271114(10)671890R; 857060 (01)00880304461611(17)280324(10)857060; 930770 (01)00880304461611(17)270725(10)930770
- Product
- Compress Device Short Anchor Plug, 26 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item…
- Recalling firm
- Biomet, Inc.
- Quantity
- N/A
- Distribution
- Worldwide distribution - US Nationwide and the countries of ARGENTINA, AUSTRALIA, CANADA, CHILE, JAPAN, NETHERLANDS, NEW ZEALAND.
- Recall date
- November 29, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)