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Smith & Nephew Inc

Smith & Nephew Inc Recalls

All product recalls associated with Smith & Nephew Inc.

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Recall Summary

Total Recalls

573

Past Year

Class I (Serious)

Most Recent

Nov 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 341–360 of 573 recalls

Smith & Nephew Inc: Exogen Express Bone Healing System, SAFHS, Part Numbers 7...

Problems with transducer may result in a reduced ultrasound output.

FDAJun 5, 2009Nationwide• Smith & Nephew Inc

Smith & Nephew, Inc. Endoscopy Division: DYONICS 25 Fluid Management System Disposable Inflow/Outf...

The sterility of the device cannot be assured

FDAMay 27, 2009PR• Smith & Nephew, Inc. Endoscopy Division

Smith & Nephew, Inc. Endoscopy Division: Smith & Nephew Endoscopic Disposable Blades: FULL RADIUS ...

Product sterility is compromised due to breach in the sterile packaging.

FDAMay 7, 2009Nationwide• Smith & Nephew, Inc. Endoscopy Division

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Smith & Nephew Inc: JOURNEY " UNI TIBIAL BASEPLATE, LEFT MEDICAL/TIGHT LATERA...

The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct.

FDAJan 23, 2009Nationwide• Smith & Nephew Inc

Smith & Nephew Inc: JOURNEY " UNI TIBIAL INSERT LEFT MEDIAL/RIGHT LATERAL, A/...

FDAJan 23, 2009Nationwide• Smith & Nephew Inc

Smith & Nephew Inc: JOURNEY " UNI TIBIAL INSERT RIGHT MEDIAL/LEFT LATERAL, A/...

FDAJan 23, 2009Nationwide• Smith & Nephew Inc

Smith & Nephew Inc: JOURNEY " UNI TIBIAL BASEPLATE, RIGHT MEDIAL/LEFT LATERAL...

FDAJan 23, 2009Nationwide• Smith & Nephew Inc

Smith & Nephew Inc: Oxinium Femoral Head, 36 MM OD-3, 12/14 Taper, REF 713436...

Radius at the end of the taper of the femoral implant is smaller than specification. This error could result in the tapers not locking fully or properly on femoral stems or in causing impingement and/or increased wear debris. The deficiency may not be noticed by the user. Impingement and/or wear debris may lead to revision.

FDAJan 23, 2009Nationwide• Smith & Nephew Inc

Smith & Nephew Inc: Smith & Nephew Orthopaedics PIP (proximal Interphalangeal...

Hinge failure: The product is cracking or breaking during use.

FDAJan 23, 2009Nationwide• Smith & Nephew Inc

Smith & Nephew Inc: LEGION Pressfit Stem, Straight, 10 MM X 160 MM, REF 71424...

Products were mispackaged.

FDAJan 22, 2009Nationwide• Smith & Nephew Inc

Smith & Nephew Inc: IMHS CP, 3.2mm, Tip Threaded Guide Pin, REF71687000, for ...

Incorrect depth gauge mark etched onto guide wire pin. Guide pin is too long.

FDAJan 22, 2009Nationwide• Smith & Nephew Inc

Rheem Oil-Fired Furnaces (Rheem) – Fire Hazard (2009)

Fire/Burn Risk

This recall involves oil-fired furnaces sold under the Rheem, Ruud and United Refrigeration brands. Only the models beginning with the model numbers listed in the chart below and with date codes ending in 0106 through 5206, 0107 through 5207, or 0108 through 4808 are included in this recall. The model number and date code (designated by the four digits following an "M" in the middle of the serial number) are printed on the unit's rating plate, which is on the left wall of the furnace's interior just above the burner. The rating plate can be found by opening the unit's burner access door, which has slotted openings. Model # Brand & Description ROBF Rheem Classic/Ruud Achiever High Efficiency Upflow Oil Furnace ROPF Rheem Classic/Ruud Achiever High Efficiency Downflow/Horizontal Oil Furnace TZOUP United Refrigeration "Thermal Zone" Upflow Oil Furnace TZODH United Refrigeration "Thermal Zone" Downflow/ Horizontal Oil Furnace

CPSCJan 22, 2009Nationwide• Air Conditioning Division of Rheem Manufacturing Co., of Fort Smith, Ark.

Smith & Nephew Inc: Tandem Unipolar, 46 MM CO-CR, REF 126646, Sterile, Smith ...

46 mm Femoral head was mismarked and packaged as being 45 mm

FDAJan 12, 2009CA, FL, MI• Smith & Nephew Inc

Smiths Medical PM, Inc. N7: Smiths Medical BCI(R) Advisor(R) Vital Signs Monitor, mod...

Recent improvements were made to the Advisor case plastic resulting in the inserts being deeply embedded into the plastic. This affects the ability of the monitor to be adequately secured on the wall mount bracket or roll stand bracket, resulting in the monitor falling off. There have been no adverse events or injuries reported.

FDADec 22, 2008FL, GA, NJ +2 more• Smiths Medical PM, Inc. N7

Smiths Medical MD, Inc.: Smiths Medical Medfusion Model 3500 Syringe Infusion Pump...

Delay in therapy. Keypad issues with Medfusion Syringe Infusion Pump, model numbers 3500-306 and 3500-415 ("Pump") have occurred during implementation or shortly after first being placed into use. These issues can be intermittent, and may render the Pump inoperable or the Pump may not respond to certain keypad button presses.

FDADec 18, 2008Nationwide• Smiths Medical MD, Inc.

Smiths Medical MD, Inc.: CADD Medication Cassette Reservoir 100 ml with Clamp and ...

Smiths Medical noticed an increased trend in leakage associated with 100 ml CADD Medication Cassette Reservoirs Reorder Number 21-7002-24 Lot Numbers 213X18 and 214X18. If a leak occurs in a CADD medication Cassette Reservoir, it may allow spillage of medication, contamination of the fluid path, and/or air to enter the Reservoir. Smiths Medical has not received any report of patient injuries due

FDADec 9, 2008PA• Smiths Medical MD, Inc.

Smith & Nephew Inc: PROMOS Reverse, Glenosphere Loosening Adapter, REF 24 000...

The product was breaking during use.

FDANov 21, 2008Nationwide• Smith & Nephew Inc

Smith & Nephew Inc: PROMOS Releasing Clamp (3 parts), REF 420 189, S&N 750066...

The product was breaking during use.

FDANov 21, 2008Nationwide• Smith & Nephew Inc

Smith & Nephew Inc: Reflection, Microstable Acetabular Liner, REF 71740250, 3...

Liners measuring 28 mm ID and were mismarked as 32 mm.

FDANov 21, 2008Nationwide• Smith & Nephew Inc

Smiths Medical MD, Inc.: Deltec Cozmo Insulin Pump, Model 1800. Deltec Cozmo Ins...

Smiths Medical has become aware of a display irregularity with the Deltec Cozmo Insulin Pump, Model 1800 and Model 21-1700 containing Model 1800 software. There have been adverse events reported that the amount of Extended Bolus delivered was not accurately displayed by the Pump. The amount of extended Bolus displayed on the Pump Home Screen 2 and in the Bolus Summary Report is less than what w

FDANov 20, 2008AL, AK, AZ +48 more• Smiths Medical MD, Inc.