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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

1000

Past Year

631

Class I (Serious)

Most Recent

Jan 2026

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 9821–9840 of 10391 recalls

Smith & Nephew Inc: Genesis II, Cruciate Retaining, Oxinium, Femoral componen...

Mispackaging-A size 5 femoral component, left, box had a size 5 right component in the box.

FDAApr 12, 2006IN, LA, NC• Smith & Nephew Inc

Northwest Medical Physics Equipment Inc: ISOLOC 6.5 Software Part Number NT-NW-425-520. Software ...

This correction was for several software bugs which caused image format problems; incorrect ruler display; software crashes; failure to update pixel spacing; display of unattainable treatment table positions; failure to update gantry angles; wrong shifts for two of three axes of treatment table movement.

FDAApr 7, 2006IN• Northwest Medical Physics Equipment Inc

Philips Medical Systems North America Co. Phillips: MD3 X-ray system

Potential for unexpected table movement.

FDAApr 6, 2006

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Nationwide

• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: MD4 X-ray system

Potential for unexpected table movement.

FDAApr 6, 2006Nationwide• Philips Medical Systems North America Co. Phillips

LandRoller Terra 9 Roller Skates (LandRoller) – Balance Design (2006)

LandRoller skates have two oversized wheels on each skate that are angled inward, which is designed to help the user keep balanced on cracked pavement and uneven surfaces. The recalled LandRoller brand skates are the "Terra 9" model manufactured between July 2005 and December 2005. The date of manufacture can be determined from the serial number, which is written on a white sticker attached to the upper inside of the right boot's plastic ankle cuff. Serial numbers beginning with "L050" are included in the recall. The brand name is on the skate's tongue and model is on the skate's rear heel area. Women's skates are purple and gray and sold in sizes 6 through 11. Men's skates are blue and black and sold in sizes 5 through 12.

CPSCApr 5, 2006Nationwide• LandRoller Inc., of Hermosa Beach, Calif.

Siemens Healthcare Diagnostics: RapidLab 1200 Systems, Model 1245 - Blood gases, electrol...

Invalid CO-oximeter values; Bayer HealthCare determined that under very specific conditions, the RapidLab 1245 or RapidLab 1265 systems may report invalid CO-oximeter values to an LIS, Rapidlink, or Rapidcomm data management system.

FDAApr 4, 2006Nationwide• Siemens Healthcare Diagnostics

Baxter Healthcare Renal Div: Baxter Healthcare Corporation, RenalSoft Observational St...

Software Error: There are software discrepancies that may increase the possibility of a medication error if the dialysis clinic software is used to track, record, or coordinate the administration of medications.

FDAMar 29, 2006Nationwide• Baxter Healthcare Renal Div

Southwest Technologies Inc: Elasto-Gel Wound Dressings, 3 product codes: DR8050, DR ...

The product is labeled as sterile and one of the lots failed sterility during the quarterly radiation dose audit.

FDAMar 27, 2006Nationwide• Southwest Technologies Inc

Smith & Nephew, Inc. Endoscopy Division: FAST-FIX AB Curved Needle Delivery System, Used for menis...

The implant consists of a T1 and T2 anchor which are joined together by a suture. The T2 portion of the implant may not advance into the deployment position preventing deployment of the T2 anchor.

FDAMar 24, 2006Nationwide• Smith & Nephew, Inc. Endoscopy Division

GE Healthcare: Fresh Gas Control (A-FGC1) Unit, a component of the S/5 A...

There exists the possibility that the ADU Fresh Gas Control unit (A-FGC1) can shut off during normal handling of the anesthesia machine and result in no anesthetic agent output.

FDAMar 22, 2006CA, FL, IL +5 more• GE Healthcare

Hitachi Medical Systems America Inc: MRP-7000, AIRIS Magnetic Resonance Imaging Systems

Software anomaly. A software defect in the referenced systems can cause a slice indicator (reference line) to be mis-positioned on the cross-reference image when it is magnified. This image error could result in a possible patient mis-diagnosis.

FDAMar 17, 2006Nationwide• Hitachi Medical Systems America Inc

Plasma Flat Panel TVs (Philips) – Potential Defect (2006)

The recall involves only certain 42- and 50-inch, 2005 model Philips branded Plasma Flat Panel Televisions with Ambilight technology, which is an ambient lighting feature that projects a soft light onto the wall behind the TV to enhance the display. They were manufactured with the following model, date codes, and serial numbers: Model Display Type Production Began Production Ended Beginning Serial Range Ending Serial Range 42PF9630A/37 Plasma April 2005 July 2005 AG1A0518xxxxxx AG1A0528xxxxxx 50PF9630A/37 Plasma May 2005 August 2005 AG1A0519xxxxxx AG1A0533xxxxxx 50PF9630A/37 Plasma June 2005 August 2005 YA1A0523xxxxxx YA1A0534xxxxxx 50PF9830A/37 Plasma June 2005 August 2005 AG1A0526xxxxxx AG1A0533xxxxxx The model and serial numbers can be found on the back of the TV on the label that looks like the example in the picture: The serial number can also be obtained by pushing the following keystrokes on the remote control: 123654, after which a customer service menu ("CSM") will be displayed on the screen. In the menu, line 03 displays the type number and line 04 displays the production code (identical to the serial number of the set). Press the MENU button on the remote to exit the CSM.

CPSCMar 16, 2006Nationwide• Philips Consumer Electronics North America, of Atlanta, Ga.

Bayer Healthcare, LLC (Diagnostics Division): ADVIA 2120 systems -Automated Complete Blood Cell and Dif...

The ADVIA 2120 has reported ; highly intermittent low results on all primary results: White Blood Cells (WBC), Red Blood Cells (RBC), Hemoglobin (HGB) and Platelets (PLT) and an abnormal baso cytogram.

FDAMar 16, 2006Nationwide• Bayer Healthcare, LLC (Diagnostics Division)

GE Healthcare: GE Healthcare Innova 3100 and Innova 3100 with Bolus Chas...

Incorrect screws were used for mounting the detector which may lead to a possible part falling onto a patient.

FDAMar 6, 2006Nationwide• GE Healthcare

GE Healthcare: GE Healthcare Innova 4100 and Innova 4100 with Bolus Chas...

Incorrect screws were used for mounting the detector which may lead to a possible part falling onto a patient.

FDAMar 6, 2006Nationwide• GE Healthcare

GE Healthcare: GE Medical Systems Innova 2000 and Innova 2000S, and Inno...

Incorrect screws were used for mounting the detector which may lead to a possible part falling onto a patient.

FDAMar 6, 2006Nationwide• GE Healthcare

Little Tikes Animal Flashlights – Lead Paint (2006)

The Glowin' Dino Flashlight and the Glowin' Doggy Flashlight are about 9 inches long and make an electronic sound when switched on. The green dinosaur roars, and the white and brown dog barks. Only flashlights with the following date codes are included in the recall: LC5H161, LC5H291, LC5I031, LC5I091, LC5I131, LC5J061, LC5J231, and LC5J311. The date codes are found on the bottom of the flashlights. Units that do not contain these codes or other animal flashlight characters made by The Little Tikes Co. are not included in this recall. Also, units that have an "R" at the end of the date code are not included in the recall.

CPSCMar 1, 2006Nationwide• The Little Tikes Co., of Hudson, Ohio

Baxter Healthcare Renal Div: System 1000 family of Hemodialysis Instruments, including...

The older style 'Through Hardware' Dialysate Monitoring Manifolds and 'Noryl' Ultra Filtration Removal Regulators may become cracked due to mechanical and thermal stress. If either of these parts become cracked during patient treatment, there is the potential for an ultrafiltration error to occur, which can result in excessive removal of fluid from the patient.

FDAFeb 24, 2006Nationwide• Baxter Healthcare Renal Div

Hitachi Medical Systems America Inc: Hitachi CXR-4 CT Computed Tomography X-ray System (includ...

The device has a software anomaly which affects the system's ability to create Multiplanar Reconstructions (MPR). Some images from the resulting series do not display correctly, or display at all, when MPR was run on them.

FDAFeb 21, 2006Nationwide• Hitachi Medical Systems America Inc

Hitachi Medical Systems America Inc: Hitachi Emission Computed Tomography System Hitachi CX-4 ...

The device has a software anomaly which causes blank images to be created during Multiplanar Reconstruction processing or results in an inherent filming error in which a reference scale is improperly sized.

FDAFeb 21, 2006CA, CT, FL +8 more• Hitachi Medical Systems America Inc