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St Jude Medical CRMD

St Jude Medical CRMD Recalls

All product recalls associated with St Jude Medical CRMD.

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Recall Summary

Total Recalls

1000

Past Year

898

Class I (Serious)

125

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 16301–16320 of 17592 recalls

St Jude Medical CRMD: CPS Aim, Models 410140, 410141, 410142, 410144, 410145, 4...

Sterility-Some of the sterile pouches in which these products are packaged may not have been properly sealed during their packaging process.

FDAJun 1, 2006AZ, CA, IN +3 more• St Jude Medical CRMD

St Jude Medical CRMD: CPS Direct SL, Models 410110, 410111, 410112, 410113, 410...

Sterility-Some of the sterile pouches in which these products are packaged may not have been properly sealed during their packaging process.

FDAJun 1, 2006AZ, CA, IN +3 more• St Jude Medical CRMD

GE Medical Systems LLC: GE Healthcare-Americas Signa 3.0T EXCITE Whole Body Magne...

To provide the 3.0T MRI systems users with the 8-channel brain coil the proper coil weighting software. The proper coil weighting factors for the eight-channel brain coil were not included in the software.

FDA

1...814 815816817 818...880

Page 816 of 880Next

Jun 1, 2006

Nationwide

• GE Medical Systems LLC

St Jude Medical CRMD: CPS Valve Bypass Tool (VBT), Model 410192

Sterility-Some of the sterile pouches in which these products are packaged may not have been properly sealed during their packaging process.

FDAJun 1, 2006AZ, CA, IN +3 more• St Jude Medical CRMD

St Jude Medical CRMD: CPS Slitter, Model 410191

Sterility-Some of the sterile pouches in which these products are packaged may not have been properly sealed during their packaging process.

FDAJun 1, 2006AZ, CA, IN +3 more• St Jude Medical CRMD

St Jude Medical CRMD: CPS Implant Kit, Model 410190

Sterility-Some of the sterile pouches in which these products are packaged may not have been properly sealed during their packaging process.

FDAJun 1, 2006AZ, CA, IN +3 more• St Jude Medical CRMD

General Electric Med Systems LLC: GE Healthcare Proteus XR/a General Purpose Radiographic ...

Labeling; failure to properly label per 21 CFR 1010.2 and 1010.3 -The Operator Console of the Proteus XR/a General Purpose Radiographic Systems were not properly labeled.

FDAMay 31, 2006Nationwide• General Electric Med Systems LLC

General Electric Med Systems LLC: GE Healthcare Definium 8000 Digital Radiographic Systems ...

An incident was reported that an operator's finger was pinched between the fixed roller and the gliding tabletop of a Proteus XR/a Table while moving the tabletop with the thumb placed over its edge and fingers underneath

FDAMay 31, 2006Nationwide• General Electric Med Systems LLC

General Electric Med Systems LLC: GE Proteus XR/a Radiographic System. GE Medical Systems-...

FDAMay 31, 2006Nationwide• General Electric Med Systems LLC

GE OEC Medical Systems, Inc: GE 4 inch Anterior Cervical Post, GE Part Number 1006385 ...

Weld defect- the weld between the post body and the screw was not properly formed and can fail, even when minimal force is used.

FDAMay 31, 2006Nationwide• GE OEC Medical Systems, Inc

General Electric Med Systems LLC: GE Healthcare Revolution XR/d; GE Healthcare, 3000 North ...

FDAMay 31, 2006Nationwide• General Electric Med Systems LLC

General Electric Med Systems LLC: GE Proteus XR/a Radiographic System. GE Medical Systems-...

Class IIModerate

FDAMay 31, 2006Nationwide• General Electric Med Systems LLC

General Electric Med Systems LLC: GE Healthcare Revolution XR/d; GE Healthcare, 3000 North ...

Class IIModerate

FDAMay 31, 2006Nationwide• General Electric Med Systems LLC

General Electric Med Systems LLC: GE Healthcare Definium 8000 Digital Radiographic Systems ...

Class IIModerate

FDAMay 31, 2006Nationwide• General Electric Med Systems LLC

Electric Smokehouse Smoker (Masterbuilt) – Fire Risk (2006)

Fire/Burn Risk

The smokers cook food slowly at lower temperatures and use wood chips to produce smoke inside the unit for flavor. Wood chips are placed inside the smoker and heated using an electric burner element to produce smoldering coals. The electric smokehouse model ESQ30B has a black powder coated outer shell with the Masterbuilt Electric Smokehouse logo on the front door. The electric smokehouse model ESQ30S has a stainless steel outer shell with the Masterbuilt Electric Smokehouse logo on the front door. The model number is located on a metal plate on the back of the unit.

CPSCMay 31, 2006Nationwide• Masterbuilt Manufacturing Inc., of Columbus Ga.

Suros Surgical Systems Inc.: ATEC Breast Biopsy and Excision System Needle Guide, 9 GA...

Lack of assurance of sterility, as package may have a seal defect (improperly sealed primary packaging).

FDAMay 25, 2006Nationwide• Suros Surgical Systems Inc.

Terang Nusa Sdn Bhd 1, Jalan 8, Pengkalan Chepa 2, Ind Zone Kota Bharu Malaysia: Sterile Triumph LT Latex Powder-Free Surgeons Gloves; 50 ...

The sterile glove pouches may have an open seal at the bottom of the pouch.

FDAMay 23, 2006Nationwide• Terang Nusa Sdn Bhd 1, Jalan 8, Pengkalan Chepa 2, Ind Zone Kota Bharu Malaysia

Arctic Cat Prowler XT Vehicle (Arctic Cat) – Utility Vehicle Issue (2006)

The Prowler XT was produced in three colors: Green, Cat Green and Red. The vehicles have the words "Arctic Cat" printed on each side of the cargo box and the name "Prowler XT" centered on the front of the hood. The affected units are all 2006 Prowler XT vehicles with VIN range of 4UF06MPVO6T300001 through 4UF06MPV16T302369. The VIN is located on the rear upper-frame tube of the vehicle near the rear of the cargo box, and on the registration materials the consumer received at the time of purchase. Consumers need only refer to the last six digits of the VIN to determine if the vehicle is included in this recall. The following model numbers are included in this recall. The model number is contained in the registration materials received with the vehicle at the time of purchase. Model Model Number Prowler XT Green U2006P2S4BUSG Prowler XT Cat Green U2006P2S4BUSZ Prowler XT Red U2006P2S4BUSR

CPSCMay 23, 2006Nationwide• Arctic Cat Inc., of Thief River Falls, Minn.

Beckman Coulter Inc: Cytomics FC 500 Flow Cytometry System Part Numbers 626553...

Beckman Coulter has determined that under certain conditions a system error generated during a Pause and Rotate routine may result in a sample misidentification with a risk of reporting erroneous results.

FDAMay 22, 2006Nationwide• Beckman Coulter Inc

Hunting Tree Stands (Primal Vantage) – Collapse Risk (2006)

The recall involves two models of tree stands: the Ameristep Patriot Hang-On Tree Stand has model number 7300, and the Outfitter Hang-On Tree Stand has model number 7310. These products are fixed-position, strap-on tree stands. The UPC number of the model 7300 is 769524703001. The UPC number of model 7310 is 769524703100. The model number and UPC are not written on the tree stands, but can be found on the packaging.

CPSCMay 18, 2006Nationwide• Primal Vantage Company Inc., of Randolph, N.J.