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FDA (Device enforcement)Recalled 2023-10-09class ii

Biomet, Inc.: Compress Device Short Anchor Plug, 16 MM- Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement Item Number: 178558

Hazard

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

Details from the source

Reason for recall: 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 Distribution: Worldwide distribution - US Nationwide and the countries of ARGENTINA, AUSTRALIA, CANADA, CHILE, JAPAN, NETHERLANDS, NEW ZEALAND. Quantity: N/A Lot/code info: Lot Numbers/UDI: 331750 (01)00880304461673(17)270726(10)331750; 331760 (01)00880304461673(17)270725(10)331760; 331770 (01)00880304461673(17)270901(10)331770; 577380 (01)00880304461673(17)270725(10)577380; 608690 (01)00880304461673(17)271030(10)608690; 671340 (01)00880304461673(17)271026(10)671340; 671350 (01)00880304461673(17)271127(10)671350; 671460 (01)00880304461673(17)271030(10)671460; 671840 (01)00880304461673(17)271117(10)671840; 735690 (01)00880304461673(17)271030(10)735690; 735720 (01)00880304461673(17)271109(10)735720; 735720R (01)00880304461673(17)271109(10)735720R; 930750 (01)00880304461673(17)270726(10)930750

UPC codes

00880304461673

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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