Smith & Nephew, Inc.: 118 recalls on record

Recalls filed with 1 agency: FDA (118).

First recall on record: September 26, 2012. Most recent: June 24, 2026.

Risk classification: Class II: 118

Most recent recalls

DateAgencyProduct
March 5, 2014FDARenasys EZ, a Canister Component of of Renasys EZ Negative Pressure Wound Therapy SystemZ-1067-2014
March 5, 2014FDAReflection Interfit Shell, 52 MM OD, 3 HOLE, REF 71336052, QTY 1, STERILE R, Smith & Neph…Z-1066-2014
January 1, 2014FDAREFLECTION(R), MICROSTABLE(R), ACETABULAR LINER, 20o OVERHANG, 28 MM ID, 54-56 OD, QTY: (…Z-0581-2014
December 11, 2013FDAGENESIS(R) II, PS HIGH FLEXION ARTICULAR INSERT, SIZE 5-6, 9 MM QTY: (1), REF 71421515,…Z-0447-2014
December 11, 2013FDAGENESIS(R) II, PS HIGH FLEXION ARTICULAR INSERT, SIZE 5-6, 11 MM QTY: (1), REF 71421516, …Z-0448-2014
December 11, 2013FDAGENESIS(R) II, POSTERIOR STABILIZED ARTICULAR INSERT, SIZE 1-2, 13 MM QTY: (1), REF 71420…Z-0444-2014
December 11, 2013FDAGENESIS(R) II, PS HIGH FLEXION ARTICULAR INSERT, SIZE 3-4, 9 MM QTY: (1), REF 71421508,…Z-0446-2014
December 11, 2013FDAGENESIS(R) II, PS HIGH FLEXION ARTICULAR INSERT, SIZE 3-4, 13 MM QTY: (1), REF 71420820,…Z-0445-2014
December 11, 2013FDAGENESIS(R) II, MOBILE BEARING ARTICULAR INSERT RIGHT, SIZE 5, 9 MM QTY: (1), REF 71621509…Z-0449-2014
November 13, 2013FDAGENESIS(R) II, NON-POROUS TIBIAL BASE, SIZE 6, RIGHT, QTY: (1), REF 71420188. Product …Z-0131-2014
November 13, 2013FDAGENESIS(R) II, NON-POROUS TIBIAL BASE, SIZE 5, LEFT, QTY: (1), REF 71420168. Product U…Z-0130-2014
August 28, 2013FDAGENESIS(R) II CRUCIATE RETAINING ARTICULAR INSERT, TRIAL, SIZE 3-4, A/P 48 MM, M/L 68 MM,…Z-1996-2013
August 14, 2013FDAR3 (TM) XLPE ACETABULAR LINER UHMWPE, 20o OVERHANG, 36 MM ID, 62 MM OD, QTY: (1), STERILE…Z-1928-2013
August 14, 2013FDAR3 (TM) XLPE ACETABULAR LINER UHMWPE, 20o OVERHANG, 36 MM ID, 60 MM OD, QTY: (1), STERILE…Z-1929-2013
April 24, 2013FDATRIGEN (TM) L-P SCREW, 4.5 MM X 37.5 MM, TI-6AL-4V, QTY: (1), STERILE R, REF 71645437, Sm…Z-1132-2013
March 20, 2013FDAINTERNAL HEX RECON SCREW, TI-6AL-4V, REF 7162375, TRIGEN (R) INTERNAL HEX CAPTURED RECON …Z-0944-2013
March 20, 2013FDAINTERNAL HEX RECON SCREW, TI-6AL-4V, REF 7162380, TRIGEN (R) INTERNAL HEX CAPTURED RECON …Z-0943-2013
September 26, 2012FDA12/14 TAPER HIGH OFFSET NECK USE WITH SMITH & NEPHEW STEMS AND 12/14 FEMORAL COMPONENTS O…Z-2427-2012

Questions about this company

How many recalls does Smith & Nephew, Inc. have?
Recalert has 118 U.S. recalls on record for Smith & Nephew, Inc., published between September 26, 2012 and June 24, 2026.
Which agencies have handled Smith & Nephew, Inc. recalls?
Smith & Nephew, Inc. appears as the recalling firm in recalls from: FDA (118).

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