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Roche Diagnostics Corp.

Roche Diagnostics Corp. Recalls

All product recalls associated with Roche Diagnostics Corp..

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Recall Summary

Total Recalls

1000

Past Year

1000

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 20681–20700 of 21319 recalls

Roche Diagnostics Corp.: Tecan clinical workstation; Tecan Genesis 150/8 front end...

Tecan software has the potential to match the patient with a different patient's test results.

FDAMay 5, 2004Nationwide• Roche Diagnostics Corp.

Boston Scientific Corp: ''NAMIC Custom Angiographic Kit'' sold under the followi...

Molded handles used in Angiographic Manifolds may be occluded.

FDAMay 5, 2004IL, IN, KY +3 more• Boston Scientific Corp

Medtronic Physio Control Corp: DC Power Adapter for use with the LIFEPAK 12 defibrillato...

The DC Power Adapter may fail to charge LIFEPAK NiCd 2.4 AH batteries used with the LIFEPAK 12 defibrillator/monitor.

FDAMay 5, 2004Nationwide• Medtronic Physio Control Corp

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Varian Medical Systems: VariSource High Dose Rate Afterloader, Models 200, 200t, ...

Manufacturer of brachytherapy instrument issued a Customer Technical Bulletin to clarify instructions for use of the radiation treatment medical device by healthcare practitioners.

FDAMay 4, 2004Nationwide• Varian Medical Systems

Cypress Medical Products, Ltd.: Manual Mechanical Wheelchair, 24'' seat, , maximum patien...

The seat of the wheelchair may come loose from the frame with the screws and the collars still attached when the seat is pulled upward to fold the wheelchair.

FDAMay 3, 2004Nationwide• Cypress Medical Products, Ltd.

Diagnostic Products Corp: Immulite 1000 CEA Catalog No. LKCE1

Instabililty

FDAMay 3, 2004Nationwide• Diagnostic Products Corp

Cypress Medical Products, Ltd.: Manual Mechanical Wheelchair, 18'' seat, , maximum patien...

The seat of the wheelchair may come loose from the frame with the screws and the collars still attached when the seat is pulled upward to fold the wheelchair.

FDAMay 3, 2004Nationwide• Cypress Medical Products, Ltd.

American Medical Systems: AMS Ambicor Penile Prosthesis, Penoscrotal Approach, Leng...

The product is mislabeled as to length.

FDAApr 29, 2004CA, IN, TX +1 more• American Medical Systems

Medtronic Gastroenterology Urology: Medtronic Gastro pH in a Box System, Model 43A008, Catalo...

Inadequate wire insulation inside the plugs of the power cords of the devices may cause the power cords to short.

FDAApr 28, 2004Nationwide• Medtronic Gastroenterology Urology

Gas Water Heater Controls (White-Rodgers) – Temperature Risk (2004)

Fire/Burn Risk

The temperature control is a small metal box located above the access panel door of the gas water heater. A white label with red lettering located on the right side of the control contains one of the following model numbers: 37C55U 658, 37C57U 602, 37C72U 520, 37C72U 546, 37C72U 547, or 37C72U 548, and 37C72U 676. There should be a four- digit metal stamped date code located below the label on the right side of the control. Recalled controls will have date codes 0240 to 0329 (40th week of 2002 to 29th week of 2003). Potentially affected gas water heaters include: AO Smith, Apollo, Crosley, Energysense, Freedom, Intertherm, Kenmore, Maytag, Mission, Myers, Penfield, President, Reliance, Sentry, or State. Beginning serial numbers on these gas water heaters can be checked at www.regcen.com/tempcontrolrecall

CPSCApr 28, 2004Nationwide• White-Rodgers, a division of Emerson Electric Co., of St. Louis, Mo.

Staar Surgical Co Inc: MicroSTAAR Injector, MSI-PF Packed ten per box.

Cracking of the distal end of the injector occurs during locking of the cartridge into the nose cone of the injector.

FDAApr 21, 2004Nationwide• Staar Surgical Co Inc

Wilson-Cook Medical Inc: Biliary Stent Introducer Set

The guiding catheter provided with the SIS-10 biliary stent introduction system may be a 5 French instead of the required 6 French guiding catheter.

FDAApr 21, 2004MO, NY, PA• Wilson-Cook Medical Inc

Wilson-Cook Medical Inc: AcuSnare Polypectomy Device, Cook Wilson-Cook Medical GI ...

The snares inside the box labeled SASM-1 may actually be ASM-1 devices. The individual pouches may be correctly labeled ASM.

FDAApr 21, 2004MA, NY, OK• Wilson-Cook Medical Inc

Accessory Electric Heaters (American Standard) – Performance Issue (2004)

Fire/Burn Risk

The 240-volt accessory heaters are used to provide supplemental heat in the heat pump or electric heating system. The accessory heater - model number BAYHTR1415BRKAC manufactured between April 14, 2003 and February 6, 2004 - is located inside the air handler cabinet usually found in the basement, attic, equipment closet or crawlspace of a consumer's home. The horizontally or vertically installed air handler is a painted metal cabinet with the Trane or American Standard name plate on its front. Air handler model numbers are found on the outside of the air handler door. Consumers with one of the recalled units are being directly contacted by the independent dealer that installed it. If you had a Trane or American Standard heat pump or electric heating system installed between April 2003 and February 2004, and have not yet been contacted by your installer, write down your air handler model number and call your installer to see whether your air handler could contain a recalled heater. You may also visit the firm's website to see whether your air handler could contain one of the recalled heaters and, if so, call your installer. To avoid electric shock, do not open the air handler door. Only a professional installer should open the air handler door to determine if you have a recalled accessory heater.

CPSCApr 20, 2004Nationwide• American Standard Companies, of Piscataway, N.J.

Braun, B Medical Inc: 18G Catheter is a component in various kits.

Catheter separated from the hub.

FDAApr 16, 2004CA, CO, FL +26 more• Braun, B Medical Inc

Philips Medical Systems Sales & Service Region No. America: Xcelera System, image processing, radiological.

Potential for the image data to be erased from the long term archive.

FDAApr 15, 2004Nationwide• Philips Medical Systems Sales & Service Region No. America

NxStage Medical, Inc.: NxStage Cartridge Express. A disposable extracorporeal bl...

Pinhole leaks on the replacement (RF) side FMP bag in certain lots of its disposable cartridge balance chambers resulting in loss of dialysate or ultrafiltrate

FDAApr 14, 2004CA, IL, IN +6 more• NxStage Medical, Inc.

Radio-Control Toy Trucks (Nikko America) – Performance Issue (2004)

Fire/Burn Risk

The recalled toy trucks were manufactured from April 2003 through January 2004. The trucks are 1/10 scale models (approximately 18 inches in length) of the Chevy Avalanche (model 100021A), the Jeep Wrangler Rubicon (model 100022A and 100022B), the Hummer Wagon (model 100023A and 100023B) and the Ford F150 (model 100024A and 100024B). Model numbers can be found on the body of the truck, along with the vehicle make and model names.

CPSCApr 13, 2004Nationwide• Nikko America Inc., of Plano, Texas

ABX Diagnostics Inc: Pentra 80 and Pentra 80XL Hematology Analyzers

Software defect, instrument may erroneously give a result of '0' or '---'.

FDAApr 8, 2004Nationwide• ABX Diagnostics Inc

Medtronic Physio Control Corp: LIFEPAK 12 defibrillator/monitor.

Potential for display to go blank due to an electrical component that may fail due to mechanical shock of vibration of the defibrillator.

FDAApr 5, 2004Nationwide• Medtronic Physio Control Corp