Zimmer, Inc.: 397 recalls on record

Recalls filed with 1 agency: FDA (397).

First recall on record: July 4, 2012. Most recent: July 1, 2026.

Risk classification: Class I: 1 · Class II: 396

Most recent recalls

DateAgencyProduct
September 4, 2013FDAVERSA-FX II FEMORAL FIXATION SYSTEM COMPRESSION TUBE/PLATE, standard and short low profil…Z-2093-2013
September 4, 2013FDAFree Lock Femoral Hip Fixation System Compression Tube/Plate, different length (59, 75, 9…Z-2091-2013
September 4, 2013FDAVERSA-FX II FEMORAL FIXATION SYSTEM COMPRESSION TUBE/PLATE, standard and short - low prof…Z-2094-2013
August 28, 2013FDA90595203117 Articular Surface XLPE CR ART SURF AE34/STYEL 17, Rx, Sterile; 90595203120…Z-2023-2013
August 28, 2013FDA00595203110 Articular Surface XLPE CR ART SURF 3,4/SYEL 10, Rx, Sterile; 00595203112 A…Z-2022-2013
August 28, 2013FDA00597503110 Provisional AC ARTSURF PROV 34/STRIPE YEL10, Rx, Sterile; 00597503112 Pro…Z-2040-2013
August 28, 2013FDA00597004109 Articular Surface CR ART SURF 56/STRIPE GREEN 9, Rx, Sterile; 00597004110 …Z-2030-2013
August 28, 2013FDA00597101101 Provisional CR PROV FRM COMP SIZE AML, Rx, Sterile; 00597101102 Provision…Z-2034-2013
August 28, 2013FDA00597106126 Provisional ALL POLY PAT PROV MICRO SZ 26, Rx, Sterile; 00597106129 Provi…Z-2037-2013
August 28, 2013FDA00595201201 Femur CR-FLEX POR FEM B-L Rx, Sterile; 00595201202 Femur CR-FLEX POR FEM …Z-2007-2013
August 28, 2013FDA00595202010 Articular Surface XLPE CR ART SURF 1,2/PUR 10, Rx, Sterile; 00595202012 Ar…Z-2016-2013
August 28, 2013FDA00597504110 Provisional AC ART SURF PROV 56/STR GRN 10, Rx, Sterile; 00597504112 Prov…Z-2041-2013
August 28, 2013FDA00597201303 Femur CR POR FM COMP SIZE CML Rx, Sterile; 00597201304 Femur CR POR FM CO…Z-2011-2013
August 28, 2013FDA00597106126 Provisional MIC POROUS PAT PROV 26MMX10MM, Rx, Sterile; 00597106129 Provi…Z-2038-2013
August 28, 2013FDA00597102010 Provisional CR ART SURF PROV 12/PURPLE 10, Rx, Sterile; 00597102012 Provi…Z-2042-2013
August 28, 2013FDA00597003109 Articular Surface CR ART SURF 34/STRIPE YEL 9, Rx, Sterile; 00597003110 Ar…Z-2024-2013
August 28, 2013FDA00597203109 Articular Surface CR ART SURF 34/STRIPE YEL 09, Rx, Sterile; 00597203110 A…Z-2026-2013
August 28, 2013FDA00587806126 Patella MICRO POROUS PAT 26MM X 10MM, Rx, Sterile; 00587806129 Patella MIC…Z-2014-2013
August 28, 2013FDA00595501201 Provisional CR-FLEX FEM PROV SZ B-L, Rx, Sterile; 00595501202 Provisional…Z-2035-2013
August 28, 2013FDA00597002009 Articular Surface CR ART SURF 12/PURPLE 9, Rx, Sterile; 00597002010 Articu…Z-2018-2013
August 28, 2013FDA65595201201 Femur CR-FLEX POR HATCP FEM B-L Rx, Sterile; 655…Z-2008-2013
August 28, 2013FDA00598706201 Provisional CRA FEM PROV/CUT GDE SZ BML, Rx, Sterile; 00598706202 Provisi…Z-2036-2013
August 28, 2013FDA00595001201 Femur CR-FLEX PCT FEM B-L Rx, Sterile; 00595001202 Femur …Z-2006-2013
August 28, 2013FDA00597201101 Femur CR POROUS FEM COMP SIZE AML Rx, Sterile; 00597201102 Femur CR POROUS…Z-2000-2013
August 28, 2013FDA00597201131 Femur CR POR SURF HDN FEM CO-NID AML Rx, Sterile; 00597201132 Femur CR POR…Z-2002-2013

Questions about this company

How many recalls does Zimmer, Inc. have?
Recalert has 397 U.S. recalls on record for Zimmer, Inc., published between July 4, 2012 and July 1, 2026.
Which agencies have handled Zimmer, Inc. recalls?
Zimmer, Inc. appears as the recalling firm in recalls from: FDA (397).

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