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Smith And Nephew, Inc. Endoscopy Division

Smith And Nephew, Inc. Endoscopy Division Recalls

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

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

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 36401–36420 of 37661 recalls

Smith And Nephew, Inc. Endoscopy Division: Endocoupler, C-Mount 30 mm Focal Length Catalog Number: ...

Endocouplers assembled with screws that cannot be effectively sterilized

FDAFeb 19, 2004AL, AZ, CA +16 more• Smith And Nephew, Inc. Endoscopy Division

Smith And Nephew, Inc. Endoscopy Division: Endocoupler C-Mount 35 mmFocal Length Catalog Number: 69...

Endocouplers assembled with screws that cannot be effectively sterilized

FDAFeb 19, 2004AL, AZ, CA +16 more• Smith And Nephew, Inc. Endoscopy Division

ATS Medical, Inc.: ATS Open Pivot Mechanical Heart Valve

Normally functioning prosthesis may have been placed on the valve holder mechanism in reverse position.

FDAFeb 18, 2004Nationwide• ATS Medical, Inc.

1...1819 182018211822 1823...1884

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Arrow International Inc: Two Lumen 14F Hemodialysis Catheter Kits/Sets with Blue F...

catheter slips out of the suture wing during use.

FDAFeb 18, 2004Nationwide• Arrow International Inc

Abbott Laboratories HPD/ADD/GPRD: TDx/TDxFLx Cortisol Reagent Pack, list 9116-65; Abbott L...

The package inserts contain incorrect control values for the urinary free cortisol extraction procedure.

FDAFeb 16, 2004IN• Abbott Laboratories HPD/ADD/GPRD

Beckman Coulter Inc: DL 2000 Data Manager, Software Version 6.2

Software defect. The type of results affected were replicate type results for a single sample transmitted within the same data stream.

FDAFeb 14, 2004Nationwide• Beckman Coulter Inc

Beckman Coulter Inc: CXP software, Part No. 623560, version 1.0

Software anomaly. Sample ID and the Run Date may become fixed within a header on the FlowPAGE printout. All samples subsequently run, with results printed using the FlowPAGE print format, will have the fixed Sample ID and Run Date, rather than the correct Sample ID and Run Date.

FDAFeb 13, 2004Nationwide• Beckman Coulter Inc

Boston Scientific Scimed: Impulse 5F 145 (degree) Multipack Angiographic Catheters,...

Some of the catheters may have yellow foreign material in their pigtail tips. The foreign material in the device could cause a stroke or significant damage to organs other than the brain.

FDAFeb 13, 2004Nationwide• Boston Scientific Scimed

Beckman Coulter Inc: Cytomics MXP Software, Version 1.0, Part No. 623688.

FDAFeb 13, 2004Nationwide• Beckman Coulter Inc

Del Medical Systems Group: DCTM Digital Ceiling Tube Mount, model DCTM; a fully coun...

There is a potentially defective worm gear in the tension adjusting mechanism of the balancer used in the Digital Ceiling Mounted Tube Support System for overhead x-ray units.

FDAFeb 13, 2004AL, AZ, CA +15 more• Del Medical Systems Group

Beckman Coulter Inc: Cytomics RXP Software, Version 1.0, Part Numbers: 175488...

FDAFeb 13, 2004Nationwide• Beckman Coulter Inc

Snowmobile Skis (Polaris) – Accessory Defect (2004)

The recalled skis are the red composite (nonmetallic) skis and were sold as an accessory item for use on Polaris snowmobiles. The part number is inscribed on the tail of the snowmobile ski. The part numbers of the skis are: Part Number Affected Part Number Stamped on Ski Replacement Black Ski (sold individually) 2872291-293 2872291-243 2872291-239 2872291-256 2872492-293 (RMK LH) 2872491-293 (RMK-RH) 1820610-243 1820610-293 5433175 5433175 5433175 5433175 5433260 5433273 5433175 5433175 2872291-070 2872291-070 2872291-070 2872291-070 2872492-070 2872491-070 2872291-070 2872291-070

CPSCFeb 12, 2004Nationwide• Polaris Industries Inc., of Medina, Minn.

Carbon Monoxide Alarms (GE Security) – Installation Issue (2004)

These ESL SafeAir 240-COE Carbon Monoxide alarms are hard-wired and require professional installation. The white, rectangular units are about 6 inches long and 2.75 inches high. "CARBON MONOXIDE ALARM" and "DO NOT PAINT" are written on the front of the units. "240-Coe, "SENTROL," (a former name of the company) and the date code are written on the back. The date code is a four-digit number ending with a "T." The four digits denote the year and week of manufacture. For example, the date code "0045T" refers to a unit that was manufactured in the 45th week of 2000. Only units with date codes 0045T (November 2000) through 0235T (August 2002) are included in the recall.

CPSCFeb 12, 2004Nationwide• GE Security, Inc., (GE Security) of Tualatin, Ore.

Stryker Howmedica Osteonics: Restoration Hip system Cylindrical Distal Extension. Cat...

The Cylindrical Distal Extensions were incorrectly coded and packaged.

FDAFeb 10, 2004Nationwide• Stryker Howmedica Osteonics

Plus Orthopedics: Biolox Ceramic Head XL

Ceramic femoral ball heads break.

FDAFeb 10, 2004CT, IN, TX• Plus Orthopedics

Luminessence T-Lite Candles (Dollar Tree) – Glass Holder Risk (2004)

Fire/Burn Risk

The recalled candles were sold in packages containing eight tea light candles and one glass holder in the shape of a flower. The 1-inch-tall candles were available in either gold or silver. A label affixed to the top of the package containing the recalled candles reads "Luminessence™ candles, 8 T-Lite Candles with Glass Holder, NET WT 3.2 oz (EACH 10G)." The label affixed to the bottom of the package reads, "DOLLAR TREE DIST., CHESAPEAKE, VA 23320, MADE IN CHINA."

CPSCFeb 10, 2004Nationwide• Dollar Tree Stores, Inc., of Chesapeake, VA

Boston Scientific Corporation: Vaxcel Port with PASV Valve, 8 Fr polyurethane catheter, ...

Reports of catheter separation/fracture after implantation resulting in distal migration of the catheter.

FDAFeb 10, 2004Nationwide• Boston Scientific Corporation

Solis Hair Dryers (Solis) – Electrical Malfunction (2004)

Laceration Risk

The recalled Solis model hair dryers include the following model numbers: 311, 340, 401, 405, 407, 407T, 411, and 415. The model name and number can be found either on the handle, the underside of the barrel or under the filter. The recalled units, which come in black and blue, do not have an immersion protection device at the end of the plug.

CPSCFeb 10, 2004Nationwide• Solis, of Switzerland

General Electric Med Systems: Seneographe 500 Mammography X-Ray Systems (all versions)

The mammography system's information for users lacked the technical specification for the minimum filtration permanently installed in the useful beam and the technical specification for the maximum line current.

FDAFeb 6, 2004Nationwide• General Electric Med Systems

General Electric Med Systems: Seneographe DMR Mammography X-Ray System (all versions)

FDAFeb 6, 2004Nationwide• General Electric Med Systems