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Bio-Rad Laboratories Inc

Bio-Rad Laboratories Inc Recalls

All product recalls associated with Bio-Rad Laboratories Inc.

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Recall Summary

Total Recalls

1000

Past Year

295

Class I (Serious)

116

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 3821–3840 of 4465 recalls

Bio-Rad Laboratories Inc: Bio-Rad Variant II TURBO Hemoglobin Testing System with C...

Sample results may be assigned to the wrong barcode number and tube position numbers, leading to discrepant sample results.

FDAOct 17, 2008Nationwide• Bio-Rad Laboratories Inc

BioSense Webster, Inc. Circuito Interior Norte, # 1820 Parque Industrial Salvarcar Cd. Juarez, Chihuahua Mexico: Biosense Webster NaviStar RMT Diagnostic/Ablation Steerab...

Biosense Webster initiated the recall because of the potential concern with one of the Printed Circuit Board (PCB) components used in the NaviStar RMT Catheters, which may cause the ablation catheter icon to shift on the map viewer when RF energy is being applied. Therefore the user, attempting a linear ablation in the location displayed on the CARTO RMT screen, may ultimately apply RF energy to u

FDAOct 2, 2008CA, CT, FL +24 more• BioSense Webster, Inc. Circuito Interior Norte, # 1820 Parque Industrial Salvarcar Cd. Juarez, Chihuahua Mexico

C. R.Bard, Inc./BardElectrophysiology Division: 7F Bard SSV 13 cm Split Sheath with Valve and sideport Ca...

1...190 191192193 194...224

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Failure to insert the guidewire through the introducer needle.

FDAOct 1, 2008Nationwide• C. R.Bard, Inc./BardElectrophysiology Division

Ski-Doo Snowmobiles (BRP) – Drive Axle Failure (2008)

This recall involves Ski-Doo® Model Year 2008 and 2009 snowmobiles. Models included in the recall are listed below. Model numbers are printed on the side panels of the snowmobiles. Ski-Doo® Model Year 2008 MXZ X 800R PowerTEK MXZ X 600HO SDI MXZ Adrenaline 800R PowerTEK MXZ Adrenaline 600HO SDI MXZ TNT 500SS MXZ Trails 500SS GSX Limited Touring 600HO SDI GSX Limited 800R PowerTEK GSX Limited 600HO SDI GSX Sport 500SS MXZ Renegade X 800R PowerTEK MXZ Renegade X 600HO SDI MXZ Renegade 800R PowerTEK MXZ Renegade 600HO SDI Summit X 800R Power TEK Summit Everest 800R PowerTEK MXZ X 600RS Ski-Doo® Model Year 2009 MXZ TNT 600HO E-TEC

CPSCSep 26, 2008Nationwide• Bombardier Recreational Products Inc., of Valcourt, Canada

B. Braun Medical, Inc.: Smallbore T-Port Extension Set with Female Luer Lock Conn...

Product was assembled incorrectly and connected to the wrong part.

FDASep 17, 2008Nationwide• B. Braun Medical, Inc.

Apeks Scuba Regulators (Aqua Lung) – drowning hazard (2008)

This recall involves Apeks TX, ATX, and XTX second stage regulators that have never been serviced. Apeks and TX, ATX, or XTX is printed on the regulator.

CPSCSep 17, 2008Nationwide• Apeks Marine Equipment Ltd., of Blackburn, England

Abbott Molecular: VP 2000 Processor; an automated tissue stainer 100 volt -...

Thermal runaway conditions, in that the target temperature was exceeded and the temperature display could not track the actual temperature within the heated slide basins of the VP 2000 Slide Processor.

FDASep 15, 2008Nationwide• Abbott Molecular

Abbott Laboratories Inc.: ABBOTT Clinical Chemistry Bilirubin Calibrator, List Numb...

The field action was initiated after an investigation for the Total Bilirubin reagents (List Number 8G62 and List Number 6L45) determined that the matrix of the secondary standard used in the value assignment of the calibrator is sensitive to the Diazo method. The matrix of this secondary standard caused a positive bias. Because of these findings, a new Total Bilirubin calibrator value assignm

FDASep 12, 2008Nationwide• Abbott Laboratories Inc.

Gas Boilers (PB Heat) – carbon monoxide risk (2008)

Fire/Burn Risk

This recall involves the DE and PSC II Gas Fired Cast Iron Boilers with the Endura Plastics Model ES2035 pressure switch used for home heating and domestic hot water heating. The boilers were available in either natural or LP gas. The boiler rating label is located on the top jacket panel on Series PSCII models and the left side jacket panel on the Series DE models. The label includes the model and serial number. The following model names and serial numbers are included in the recall: Model Name Serial Number DE-03, DE-04, DE-05 and DE-06 5040768 to 5052860 PSCII-03, PSCII-04, PSCII-05, and PSCII-06 5040777 to 5052166 Other suffix designation may follow the base model number, such as SV-WPC.

CPSCSep 11, 2008Nationwide• PB Heat LLC, of Bally, Pa.

Barcoview 35 President Kennedy Park Kortrijk Belgium: Barco Surgical Display, Model MDSC-2124 The 24-inch MDSC...

The front protective cover may loosen and completely fall off.

FDASep 9, 2008Nationwide• Barcoview 35 President Kennedy Park Kortrijk Belgium

Abbott Laboratories, Inc: ACCELERATOR APS Centrifuge Module (Hettich Robotic centri...

ACCELERATOR APS Centrifuge Module being recalled due to potential for micro-cracks to form over time in the metal centrifuge rotor buckets that may cause the centrifuge buckets to disconnect from the rotor in the centrifuge during centrifugation.

FDASep 9, 2008Nationwide• Abbott Laboratories, Inc

Abbott Laboratories: Architect LH MasterCheck (List 6C25-05). An in-vitro dia...

The values listed in the Architect LH MasterCheck, Lot 82520 data sheet are incorrect. When MasterChecks do not perform as intended, the integrity of the system cannot be verified and patient results would not be generated. Other commercially available materials are available to customers in order to meet CLIA requirements.

FDASep 5, 2008Nationwide• Abbott Laboratories

Abbott Laboratories: CELL-DYN Sapphire Hematology Analyzer, List numbers 08H00...

Fire/Burn Risk

Exposed wire resulted in minor electrical shock and burn to the service technician

FDAAug 25, 2008Nationwide• Abbott Laboratories

Bio-Rad Laboratories: Rubella IgG EIA test kit, containing 1 Rubella IgG Microp...

Elevated optical density (OD) values with the kit Negative Control.

FDAAug 20, 2008Nationwide• Bio-Rad Laboratories

Bio-Rad Laboratories: Bio-Rad's Monolisa (TM) Anti-HBs EIA test kit, Labeled as...

The package insert provided with this kit contains a typographical error, giving incorrect directions to prepare a Working Conjugate Solution. If these directions are followed, it would result in a 1:6 dilution and invalidate the assay.

FDAAug 11, 2008Nationwide• Bio-Rad Laboratories

Wooden Cribs (Mother Hubbard's) - Fall Risk (2008)

The recall includes the following wooden full-size cribs: "Enchantment" (model #210), "Hush a Bye" (model #215), "Once upon a time" (model #320) and "Rock a bye" (model #1900-350). Only date codes from 0306 through 0308 are included in this recall. "Mother Hubbard's Cupboards", the model number and date code are printed on a label located on the bottom inside of the right side.

CPSCAug 5, 2008Nationwide• Mother Hubbard's Cupboards, of Toronto, Canada

Baxter Bioscience: FloSeal Endoscopic Applicator , Product Code 1500181. Th...

The recall is being conducted as a precautionary measure due to potential discoloration of the FloSeal material noted in six (6) non-medical complaints during delivery by the Endoscopic Applicator.

FDAJul 31, 2008Nationwide• Baxter Bioscience

Bio-Rad Laboratories: Kallestad (TM) Mouse Stomach/Kidney, catalog number 30443...

The Homogeneous Positive control was released with a titer of 1:256 rather than the titer value of 1:128 reported on the QC Report Label included with each test kit.

FDAJul 29, 2008Nationwide• Bio-Rad Laboratories

Bio-Rad Laboratories: Kallestad (TM) HEp-2 Cell Line Substrate. Product labele...

The Homogeneous Positive control was released with a titer of 1:256 rather than the titer value of 1:128 reported on the QC Report Label included with each test kit.

FDAJul 29, 2008Nationwide• Bio-Rad Laboratories

Bio-Rad Laboratories: Kallestad (TM) Mouse Kidney. Product labeled "BIO-RAD Ka...

The Homogeneous Positive control was released with a titer of 1:256 rather than the titer value of 1:128 reported on the QC Report Label included with each test kit.

FDAJul 29, 2008Nationwide• Bio-Rad Laboratories