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
August 28, 2013FDA65597201101 Femur CR POR FEM HATCP SIZE AML Rx, Sterile; 65597201102 Femur CR POR FE…Z-2003-2013
August 28, 2013FDA00597103110 Provisional CR ART SURF PROV 34/STR YEL 10, Rx, Sterile; 00597103112 Prov…Z-2043-2013
August 28, 2013FDA90595204117 Articular Surface XLPE CR ART SURF AE56/STGRN 17, Rx, Sterile; 90595204120…Z-2029-2013
August 28, 2013FDA65597201333 Femur CR POR FEM SURF HDN HATCP CML, Rx, Sterile; 65597201334 Femur CR POR…Z-2013-2013
August 28, 2013FDA00597604110 Articular Surface AC ART SURF 56/STRIPED GRN 10, Rx, Sterile; 00597604112 …Z-2033-2013
August 28, 2013FDA00597603110 Articular Surface AC ART SURF 34/STRIPED YEL 10, Rx, Sterile; 00597603112 …Z-2027-2013
August 28, 2013FDA00597202009 Articular Surface CR ART SURF 12/PURPLE 09, Rx, Sterile; 00597202010 Artic…Z-2020-2013
August 28, 2013FDA00597204109 Articular Surface CR ART SURF 56/STRIPE GRN 9, Rx, Sterile; 00597204110 Ar…Z-2032-2013
August 28, 2013FDA00597001101 Femur CR PRECOAT FEM COMP SIZE AML, Rx, S…Z-1998-2013
August 28, 2013FDA00595601201 Femur CR-FLEX OPT FEM B-L Rx Sterile; 00595601202 Femur CR-FLEX OPT FEM …Z-2005-2013
August 28, 2013FDA00597206126 Patella ALL POLY PAT COMP MICRO 26DIA, Rx, Sterile; 00597206129 Patella AL…Z-2015-2013
August 28, 2013FDA00597001131 Femur CR PRC SURF HDN FEM CO-NID AML, Rx,…Z-1999-2013
August 28, 2013FDA00597601201 Femur CRA PRECOAT FEM COMP SIZE B/L Rx, Sterile; 00597601202 Femur CRA PRE…Z-2004-2013
August 28, 2013FDA90597003109 Articular Surface CR ART SURF 34/STR YEL 09MM, Rx, Sterile; 90597003110 Ar…Z-2025-2013
August 28, 2013FDA00597201333 Femur CR POR SURF HDN FEM CO-NID CML, Rx, Sterile; 00597201334 Femur CR PO…Z-2012-2013
August 28, 2013FDA90595202017 Articular Surface XLPE CR ART SURF AE12/PUR 17, Rx, Sterile; 90595202020 A…Z-2017-2013
August 28, 2013FDA00597104110 Provisional CR ART SURF PROV 56/STR GRN 10, Rx, Sterile; 00597104112 Prov…Z-2044-2013
August 28, 2013FDA00597001303 Femur CR PRC FEM COMP SIZE CML Rx, Sterile; 00597001304 Femur CR PRC FEM…Z-2009-2013
August 28, 2013FDA90597004109 Articular Surface CR ART SURF AE56/STR GRN 09MM, Rx, Sterile; 90597004110 …Z-2031-2013
August 28, 2013FDA00597001333 Femur CR PRC SURF HDN FEM CO-NID CML Rx, Sterile; 00597001334 Femur CR PR…Z-2010-2013
August 28, 2013FDA00597502010 Provisional AC ART SURF PROV 12/PUR 10, Rx, Sterile; 00597502012 Provisio…Z-2039-2013
August 28, 2013FDA90597002009 Articular Surface CR ART SURF 12/PURPLE 09MM, Rx, Sterile; 90597002010 Art…Z-2019-2013
August 28, 2013FDAMoore Hip Prosthesis Long Fenestrated Stem, several head Diameter, 203 mm Stem length. …Z-1981-2013
August 28, 2013FDA00597602010 Articular Surface AC ART SURF 12/PUR 10, Rx, Sterile; 00597602012 Articula…Z-2021-2013
August 28, 2013FDA65597201131 Femur CR POR FEM SURF HDN HATCP AML Rx, Sterile; 65597201132 Femur CR POR…Z-2001-2013

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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