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Smith And Nephew, Inc. Wound Management Division

Smith And Nephew, Inc. Wound Management Division Recalls

All product recalls associated with Smith And Nephew, Inc. Wound Management Division.

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Recall Summary

Total Recalls

232

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 181–200 of 232 recalls

Smith And Nephew, Inc. Wound Management Division: GlobTek, Inc. Power Supply for Medical Use Part No: TR9CE...

External battery chargers used with the Version 29 VISTA Negative Pressure Wound Therapy pumps are failing to properly charge the pump's battery.

FDAAug 7, 2008Nationwide• Smith And Nephew, Inc. Wound Management Division

Smith & Nephew Inc: Caption Disposable Platelet Concentrator Kit, Ref 711782...

Product contained a syringe whose package seal integrity can be adversely affected when the product is exposed to low atmospheric pressure. This may occur during shipping.

FDAAug 5, 2008Nationwide• Smith & Nephew Inc

Bard Peripheral Vascular Inc: Bard Recovery Cone Removal System, Catalog Numbers: RC-1...

This action is being taken because the product has a potential for the handle to detach. The handle detachment may result in the device unable to retrieve the filter or foreign body.

1...8 91011 12

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FDAMay 9, 2008Nationwide• Bard Peripheral Vascular Inc

Smith & Nephew Inc: TRIGEN Hind Foot Fusion Nail, 10mm X 25mm Left, REF 71701...

One of the distal locking screw holes on a hindfoot fusion nail was drilled with an incorrect trajectory.

FDAApr 22, 2008Nationwide• Smith & Nephew Inc

Smith And Nephew, Inc. Wound Management Division: FLAT DRAIN -10MM, CHARIKER-JETER DRESSING KITS (LARGE AND...

Incorrect labeling. Kit labels may incorrectly state that a flat drain is contained as a kit component while some kits may contain a round drain.

FDAMar 31, 2008Nationwide• Smith And Nephew, Inc. Wound Management Division

Nanosphere, Inc.: Warfarin Metabolism Nucleic Acid Test Cartridge; Part Num...

Aberrant Results: A warfarin 2C9*2 mutant capture signal was found to be high enough to result in an aberrant result (i.e., wild-type called heterozygous).

FDAFeb 25, 2008Nationwide• Nanosphere, Inc.

Smith And Nephew, Inc. Wound Management Division: Smith & Nephew, Inc., Exu-Dry Wound Burn Dressing, Produc...

Sterility (package integrity) compromised: Distribution of product that did not meet specifications; open seals.

FDANov 21, 2007Nationwide• Smith And Nephew, Inc. Wound Management Division

Smith & Nephew, Inc. Endoscopy Division: Smith & Nephew, CALAXO Bioabsorbable lnterference Screw, ...

Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation.

FDAAug 21, 2007Nationwide• Smith & Nephew, Inc. Endoscopy Division

Smith & Nephew Inc: Smith + Nephew, Birmingham Hip Resurfacing, Acetabular Cu...

The carton label may not reflect the correct size of the acetabular cup.

FDAJul 12, 2007Nationwide• Smith & Nephew Inc

Smith & Nephew, Inc Endoscopy Division: Smith & Nephew, 420XL Xenon Light Source, 180 Watt; for e...

Several units were manufactured using a power supply that contains a 1 amp fuse where a 5 amp fuse is required. When the unit's power supply draws more that 1A, the fuse will fail causing the light to cease operating. The problem can occur anytime: from the initial turning on (powering up), to anytime during use.

FDAApr 9, 2007IN• Smith & Nephew, Inc Endoscopy Division

Smith & Nephew Inc: Smith + Nephew, Birmingham Hip Resurfacing, Acetabular Cu...

The carton label reads BHR Acetabular Cup 60mm contained a 58mm cup.

FDAMar 13, 2007Nationwide• Smith & Nephew Inc

Smith & Nephew, Inc. Endoscopy Division: Smith & Nephew Suture Passer 12 inch Part Number: 7209166

Product is labeled as reusable but there is a potential that the cannulated handle of the product cannot be cleaned adequately following use.

FDAMar 1, 2007Nationwide• Smith & Nephew, Inc. Endoscopy Division

Smith & Nephew, Inc. Endoscopy Division: Smith & Nephew Suture Passer 2 inch Part Number : 7209167

Product is labeled as reusable but there is a potential that the cannulated handle of the product cannot be cleaned adequately following use.

FDAMar 1, 2007Nationwide• Smith & Nephew, Inc. Endoscopy Division

Smith & Nephew, Inc. Endoscopy Division: RF Denervation Probe, 10 cm, temperature sensing electrod...

Product is non-sterile but labeled incorrectly as sterile.

FDAJan 19, 2007Nationwide• Smith & Nephew, Inc. Endoscopy Division

Smith & Nephew, Inc. Endoscopy Division: RF Denervation Probe, 5cm, temperature sensing electrodes...

Product is non-sterile but labeled incorrectly as sterile.

FDAJan 19, 2007Nationwide• Smith & Nephew, Inc. Endoscopy Division

Smith & Nephew, Inc Endoscopy Division: SOPRO Camera Control Units, PAL, SV420P, REF (Catalog) #7...

Surgical camera control units were not designed and manufactured to pass the IEC 60101 testing for electrical fast transients (EFT)

FDAJan 19, 2007Nationwide• Smith & Nephew, Inc Endoscopy Division

Smith & Nephew, Inc Endoscopy Division: SOPRO Camera Control Units, NTSC, SV420P; REF (Catalog) #...

Surgical camera control units were not designed and manufactured to pass the IEC 60101 testing for electrical fast transients (EFT)

FDAJan 19, 2007Nationwide• Smith & Nephew, Inc Endoscopy Division

Smith & Nephew, Inc. Endoscopy Division: RF Denervation Probe, 15 cm, temperature sensing electrod...

Product is non-sterile but labeled incorrectly as sterile.

FDAJan 19, 2007Nationwide• Smith & Nephew, Inc. Endoscopy Division

Bard Peripheral Vascular Inc: G2 Filter System - Jugular/Subclavian Delivery Kit, for u...

This action is being taken because BPV has recently received three complaints for the device that involve reports of introducer sheath tip damage. The damage may result in loss of tip integrity.

FDADec 20, 2006Nationwide• Bard Peripheral Vascular Inc

Bard Peripheral Vascular Inc: Recovery G2 Filter System - Jugular/Subclavian Delivery K...

This action is being taken because BPV has recently received three complaints for the device that involve reports of introducer sheath tip damage. The damage may result in loss of tip integrity.

FDADec 20, 2006Nationwide• Bard Peripheral Vascular Inc