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 13, 2014FDATapered-Screw Vent Implant, HA, 4.7mmD x 8mmL x 4.5mm, Part No. TSVWH8 Dental implant co…Z-2144-2014
August 6, 2014FDAZimmer Periarticular Locking Plate System Distal Radial Volar Plate Lateral Column (1st g…Z-2131-2014
July 23, 2014FDAZimmer Dental Tapered Screw-Vent Implant, Catalog TSVT6B13, Lot 62284006Z-2050-2014
July 16, 2014FDAZimmer M/L Taper Reduced Neck Standard & Extended Offset, HIP JOINT PROSTHESIS, Sizes:4,…Z-2034-2014
July 16, 2014FDAZimmer M/L Taper Hip Stem Standard & Extended Offset, HIP JOINT PROSTHESIS, Sizes: 5.0, …Z-2033-2014
July 16, 2014FDAZimmer M/L Taper Hip Prosthesis with Kinectiv Technology, HIP JOINT PROSTHESIS¿, Sizes:4…Z-2035-2014
July 9, 2014FDANexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoa…Z-1939-2014
July 9, 2014FDANexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoa…Z-1932-2014
July 9, 2014FDANexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoa…Z-1935-2014
July 9, 2014FDANexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoa…Z-1937-2014
July 9, 2014FDANexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoa…Z-1936-2014
July 9, 2014FDANexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoa…Z-1933-2014
July 9, 2014FDANexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoa…Z-1934-2014
July 9, 2014FDANexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoa…Z-1938-2014
July 9, 2014FDANexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoa…Z-1931-2014
July 2, 2014FDAVerSys¿ Hip System, Beaded Fullcoat Stems, Zimmer, Inc., Warsaw, IN 46581Z-1842-2014
May 21, 2014FDACartilage Knee Brace***LATEX FREE" Product Usage: Used in the treatment and suppor…Z-1604-2014
May 21, 2014FDAHinged Knee Support***LATEX FREE" Product Usage: Provide added lateral stability and …Z-1605-2014
May 21, 2014FDATennis Elbow Support, Neoprene***LATEX FREE" Product Usage: Provides compression and…Z-1606-2014
May 21, 2014FDADROP LOK" Knee Brace***LATEX FREE" Product Usage: Used in the treatment, support, an…Z-1603-2014
April 30, 2014FDATRABECULAR METAL MODULAR ACETABULAR SYSTEM, Shell with Cluster Holes, Porous 60mm. Cat…Z-1496-2014
March 26, 2014FDAApollo" Revision/Constrained Knee System: SZ0-16MM AK CCK TIB INSER SZ1-11MM AK CCK TIB…Z-1261-2014
March 26, 2014FDAMOST Options" System (MOST) HINGED TIB INS SZ 1 16MM HINGED TIB INS SZ 4 6MM M HINGED …Z-1250-2014
March 26, 2014FDAApollo Knee Tibial Baseplate/Knee Tibial Insert: CONG TIB INS SZ0/19MM APO CONG TIB INS…Z-1259-2014
March 26, 2014FDANatural-Knee¿ Congruent Tibial Insert with Screw: SF-CON TIB INS LT SZ1/2 1 SF-CON TIB …Z-1254-2014

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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