How many recalls does Biomet, Inc. have?

Recalert has 120 U.S. recalls on record for Biomet, Inc., published between September 26, 2012 and August 12, 2026.

Which agencies have handled Biomet, Inc. recalls?

Biomet, Inc. appears as the recalling firm in recalls from: FDA (120).

Biomet, Inc.: 120 recalls on record

Recalls filed with 1 agency: FDA (120).

First recall on record: September 26, 2012. Most recent: August 12, 2026.

Risk classification: Class II: 119 · Class III: 1

Most recent recalls

Date	Agency	Product	Recall number
July 17, 2013	FDA	REF 154223 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size D5 ARCOM UHMWP…Z-1712-2013	Z-1712-2013
July 17, 2013	FDA	REF 154203 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size A6 ARCOM UHMWP…Z-1698-2013	Z-1698-2013
July 17, 2013	FDA	REF 154237 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size F5 ARCOM UHMWP…Z-1722-2013	Z-1722-2013
July 17, 2013	FDA	REF 154231Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size E6 ARCOM UHMWPE…Z-1718-2013	Z-1718-2013
June 26, 2013	FDA	Superior Approach Resection Guide Assembly. Indicated for primary, fracture, or revisi…Z-1548-2013	Z-1548-2013
June 26, 2013	FDA	Biomet Trauma Phoenix Retrograde Femoral Connecting Bolt Trauma Fixation Systems. Prod…Z-1547-2013	Z-1547-2013
June 12, 2013	FDA	Active Articulation E1. Intended for use with either primary or revision hip arthropla…Z-1465-2013	Z-1465-2013
March 20, 2013	FDA	REF S313152 Straight Acetabular Inserter Handle Ringloc non-sterile Orthopedic manual…Z-0925-2013	Z-0925-2013
February 6, 2013	FDA	TUNNELOC ROUND HEAD INTERFERENCE SCREW 8MMX25MM Biomet Sports Medicine manufactures a v…Z-0753-2013	Z-0753-2013
January 16, 2013	FDA	PT113950 PT HYBRID Glenoid Post Regenerex porous titanium construct Sterile R Prosth…Z-0660-2013	Z-0660-2013
December 26, 2012	FDA	Biomet Offset Tibial Tray 2.5 mm Adaptor, REF 141490 Sterile, QTY.1 Product Usage: K…Z-0533-2013	Z-0533-2013
December 26, 2012	FDA	EBI XFIX DFS Rail System (Adult Rail Gradual Swivel Clamp). The Biomet Rail System consis…Z-0527-2013	Z-0527-2013
December 12, 2012	FDA	OSS Reamer Sleeve REF132-472661 KNEE REAMER SLEEVE 8.0 THRU 12.5 STAINLESS STEEL The O…Z-0471-2013	Z-0471-2013
December 12, 2012	FDA	OSS Reamer Sleeve REF132-472662 KNEE REAMER SLEEVE 13.0 thru 20.0 STAINLESS STEEL T…Z-0472-2013	Z-0472-2013
December 12, 2012	FDA	Bio-Modular Humeral Head 48mm x 24mm Ti 6AI4V/Ion Implanted (Orthopedic Implant) Produ…Z-0474-2013	Z-0474-2013
December 5, 2012	FDA	Echo Bi-Metric Press-Fit Stems/Echo Bi-Metric 11mm x 135mm Collarless Porous Stem (Orthop…Z-0442-2013	Z-0442-2013
November 28, 2012	FDA	Ranawat/Burnstein Acetabular Shell 54mm/Limited Holes/Porous Coated is a metallic, full-…Z-0415-2013	Z-0415-2013
October 10, 2012	FDA	Optilock 2.7 mm Screw Inserter. Intended Use: The OptiLock Upper Extremity Plating Sys…Z-2485-2012	Z-2485-2012
October 10, 2012	FDA	Optilock T15 AO Driver (3.5mm). Intended Use: The OptiLock Upper Extremity Plating Sys…Z-2486-2012	Z-2486-2012
September 26, 2012	FDA	JUGGERKNOT IN¿GUIDE PUNCH, 2.9MM. The JuggerKnot 2.9mm In-Guide Punch is intended to b…Z-2399-2012	Z-2399-2012

Questions about this company

How many recalls does Biomet, Inc. have?: Recalert has 120 U.S. recalls on record for Biomet, Inc., published between September 26, 2012 and August 12, 2026.
Which agencies have handled Biomet, Inc. recalls?: Biomet, Inc. appears as the recalling firm in recalls from: FDA (120).

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Biomet, Inc.: 120 recalls on record

Most recent recalls

Questions about this company

Do you carry products from Biomet, Inc.? Check your whole catalog free against 80,000+ recalls.

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