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
April 26, 2017FDAD-RAD, 1.8MM X 16MM, LOCKING PEG, QTY: (1), STERILE R, RES 74671816 OrthopedicZ-1855-2017
April 26, 2017FDASmith & Nephew ACUFEX TRUNAV Retrograde Drill 8.5MM Product Number: 72204043 The ACUFE…Z-1844-2017
April 26, 2017FDASmith & Nephew ACUFEX TRUNAV Retrograde Drill 12MM Product Number: 72204050 The ACUFEX …Z-1851-2017
April 26, 2017FDASmith & Nephew ACUFEX TRUNAV Retrograde Drill 6.5MM Product Number: 72204039 The ACUFEX…Z-1840-2017
April 26, 2017FDASmith & Nephew ACUFEX TRUNAV Retrograde Drill 8MM Product Number: 72204042 The ACUFEX …Z-1843-2017
April 26, 2017FDASmith & Nephew ACUFEX TRUNAV Retrograde Drill 7.5MM Product Number: 72204041 The ACUFEX…Z-1842-2017
April 26, 2017FDASmith & Nephew ACUFEX TRUNAV Retrograde Drill 7MM Product Number: 72204040 The ACUFEX T…Z-1841-2017
April 26, 2017FDASmith & Nephew ACUFEX TRUNAV Retrograde Drill 10MM Product Number: 72204046 The ACUFEX …Z-1847-2017
April 26, 2017FDASmith & Nephew ACUFEX TRUNAV Retrograde Drill 11MM Product Number: 72204048 The ACUFEX …Z-1849-2017
March 1, 2017FDASmith & Nephew Dyonics Saw Blade, Standard, Product Number 3701Z-1239-2017
March 1, 2017FDASmith & Nephew Dyonics Saw Blade, Short, Product Number 3703Z-1241-2017
March 1, 2017FDASmith & Nephew Dyonics Saw Blade, Narrow, Product Number 3705Z-1243-2017
March 1, 2017FDASmith & Nephew Dyonics Saw Blade, Short, Narrow, Product Number 3704Z-1242-2017
March 1, 2017FDASmith & Nephew Dyonics Saw Blade, Long, Special, Product Number 3706Z-1244-2017
March 1, 2017FDASmith & Nephew Dyonics Saw Blade, Standard, Thick, Product Number 3702Z-1240-2017
January 25, 2017FDASmith & Nephew, RENASYS GO Negative Pressure Wound Therapy External Power Supply Unit, Rx…Z-1042-2017
January 18, 2017FDAREFLECTION(R) DEAD BLOW MALLET, REF 71362106, QTY: (1), NON-STERILE, Smith & Nephew, Inc,…Z-1008-2017
January 11, 2017FDAModular Necks: The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems are indicated for …Z-0946-2017
January 11, 2017FDAModular REDAPT(TM) Hip Systems The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems …Z-0944-2017
November 9, 2016FDATANDEM (TM) COCR SHELL UHMWPE LINER BIPOLAR, REF NUMBERS: 71322040, 71322041, 713220…Z-0350-2017
November 9, 2016FDATANDEM (TM) INTL COCR SHELL UHMWPE LINER BIPOLAR, REF NUMBERS: 71324038, 71324039, 7…Z-0351-2017
September 28, 2016FDARENASYS Sterile Transparent Film and all the RENASYS Dressing kits that contains the RENA…Z-2848-2016
August 3, 2016FDASPHERICAL HEAD REFLECTION(R) 6.5 MM CANCELLOUS SCREW, REF 71332525, QTY: (1), STERILE R, …Z-2297-2016
July 6, 2016FDALEGION(TM) HK FEMORAL ASSEMBLY, SIZE 5 LEFT, A/P 62 MM, M/L 70 MM, REF 71421375 The LE…Z-2094-2016
July 6, 2016FDALEGION(TM) HK FEMORAL ASSEMBLY, SIZE 3 LEFT, A/P 54.5 MM, M/L 62 MM, REF 71421373 The …Z-2090-2016

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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