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
December 26, 2012FDAPersona, The Personalized Knee System, Tibial Sizing Plate, Cemented, Nonsterile, Size …Z-0551-2013
December 26, 2012FDAPersona The Personalized Knee System, Natural Tibia, Cemented, 5 Degree Stemmed Tivaniu…Z-0541-2013
December 26, 2012FDAPersona The Personalized Knee System, Natural Tibia, Cemented, 5 Degree Stemmed Tivaniu…Z-0539-2013
December 26, 2012FDAPersona The Personalized Knee System, Natural Tibia, Cemented, 5 Degree Stemmed Tivaniu…Z-0540-2013
December 26, 2012FDAPersona, The Personalized Knee System, Tibial Drill Guide, Cemented, 15.7 mm Diameter, …Z-0546-2013
December 26, 2012FDAPersona, The Personalized Knee System, Tibial Sizing Plate, Cemented, Nonsterile, Size …Z-0550-2013
December 26, 2012FDAPersona, The Personalized Knee System, Tibial Sizing Plate, Cemented, Nonsterile, Size …Z-0554-2013
December 26, 2012FDAPersona The Personalized Knee System, Natural Tibia, Cemented, 5 Degree Stemmed Tivaniu…Z-0542-2013
December 26, 2012FDACoonrad/Morrey New Ulnar Revision Kit for Use with Non-Interchangeable Regular Humerals S…Z-0538-2013
December 26, 2012FDAPersona, The Personalized Knee System, Tibial Broach, Cemented, Size E-F, Nonsterile, …Z-0548-2013
December 26, 2012FDAPersona, The Personalized Knee System, Tibial Sizing Plate, Cemented, Nonsterile, Size …Z-0555-2013
December 26, 2012FDACOONMAD/MORREY TOTAL ELBOW ELBOW COMPONENT REPLACEMENT SET BUSHINGS & PINS FOR USE W/SI…Z-0537-2013
December 26, 2012FDAPersona The Personalized Knee System, Natural Tibia, Cemented, 5 Degree Stemmed Tivaniu…Z-0543-2013
December 5, 2012FDANexGen CompleteKnee Solution Stemmed Nonaugmentable Tibial component The NexGen¿¿ syst…Z-0437-2013
November 28, 2012FDA. 00789502801 VerSys Femoral Head Provisional 28mm -3.5 00789502802 VerSys Femoral Head …Z-0391-2013
November 28, 2012FDA00780304001 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780304002 MIS 12/14 Slo…Z-0400-2013
November 28, 2012FDAThe Trilogy Acetabular System Shell with Cluster Holes Porous 56 mm O.D. Sterile …Z-0416-2013
November 28, 2012FDA. 00789503601 VerSys Femoral Head Provisional 36mm -3.5 00789503602 VerSys Femoral Head …Z-0393-2013
November 28, 2012FDA00780303201 MIS 12/14 Slotted Femoral Head Provisional -3.5X32 00780303202 MIS 12/14 Slo…Z-0398-2013
November 28, 2012FDA00780302201 MIS 12/14 Slotted Femoral Head Provisional -2X22 00780302202 MIS 12/14 Slott…Z-0395-2013
November 28, 2012FDA00780302601 MIS 12/14 Slotted Femoral Head Provisional -3.5X26 00780302602 MIS 12/14 Slo…Z-0396-2013
November 28, 2012FDA00789503201 VerSys Femoral Head Provisional 32mm -3.5 00789503202 VerSys Femoral Head Pr…Z-0392-2013
November 28, 2012FDAProduct 100789502202 VerSys Femoral Head Provisional 22mm +0 00789502203 VerSys Femoral …Z-0389-2013
November 28, 2012FDA00789504001 VerSys Femoral Head Provisional 40mm -3.5 00789504002 VerSys Femoral Head Pr…Z-0394-2013
November 28, 2012FDA00789502601 VerSys Femoral Head Provisional 26mm -3.5 00789502602 VerSys Femoral Head Pr…Z-0390-2013

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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