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Bio-Rad Laboratories

Bio-Rad Laboratories Recalls

All product recalls associated with Bio-Rad Laboratories.

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Recall Summary

Total Recalls

1000

Past Year

100

Class I (Serious)

Most Recent

Dec 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 2281–2300 of 2670 recalls

Bio-Rad Laboratories: BIOPLEX 2200 EBV IgG KIT, CALIBRATORS, AND CONTROLS: 100 ...

False negative results due to reagent packs exhibiting low signal.

FDANov 13, 2007Nationwide• Bio-Rad Laboratories

Bio-Rad Laboratories: BIOPLEX 2200 EBV IgM KIT, CALIBRATORS, AND CONTROLS: 100 ...

False negative results due to reagent packs exhibiting low signal.

FDANov 13, 2007Nationwide• Bio-Rad Laboratories

Bio-Rad Laboratories: BIOPLEX 2200 MULTI-ANALYTE DETECTION SYSTEM: a) 100 test ...

False negative results due to reagent packs exhibiting low signal.

FDANov 13, 2007Nationwide• Bio-Rad Laboratories

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Bio-Rad Laboratories: BIOPLEX 2200 SYPHILIS IgG Kit: 100 tests - Catalog No. 66...

False negative results due to reagent packs exhibiting low signal.

FDANov 13, 2007Nationwide• Bio-Rad Laboratories

Honda Lawn Mowers – Fire Hazard (2007)

Fire/Burn Risk

The recall involves HRX walk-behind lawn mowers with model numbers HRX217KHXA and HRX217KHMA. Only serial numbers from 1400001 through 1453714 are included in the recall. The model and serial number are printed on a label located on the upper rear of the deck. The lawn mower is dark gray with a red engine cover.

CPSCNov 8, 2007Nationwide• American Honda Motor Corp., of Torrance, Calif.

Elite Operations Toys – Lead Paint Violation (2007)

The recall involves four military-style Elite Operations toys, including Super Rigs (#1004), Command Patrol Center (#1020), Barracuda Helicopter (#1023), and 3-Pack 8-inch Figures (#1024). The product number is located on the toy's packaging.

CPSCOct 31, 2007Nationwide• Toy World Group Ltd/Chun Tat Toys Factory Limited, of Guangdong, China

Abbott Laboratories, Inc: Abbott, ACCELERATOR Device Manager (ADM); List Number: 08...

Sample/Patient Mis-identification: Two issues identified related to the ACCELERATOR Decision Manager (ADM), to include: 1) Sample Identification (SID) and/or Patient Identification (PID) numbers that contain more than 12 characters are truncated to the final 12 characters by the ADM; 2) for SIDs using alpha characters that are case sensitive, SIDs with lower case characters are transmitted by the

FDAOct 25, 2007Nationwide• Abbott Laboratories, Inc

Children's Toy Garden Tools (Jo-Ann) – Lead Paint (2007)

This recall involves the Robbie Ducky children's leaf rake, hoe, broom and spade. "Robbie Ducky™ Garden Collection" is printed on a tag attached to the handle. The rake has a yellow handle with the head of a tortoise and green prongs. The hoe has an orange handle with a caterpillar and a blue blade. The broom has a purple handle with a duck and an orange brush. The spade has a yellow handle with the head of a frog and a red blade. The tools measure between 27 and 29 inches long.

CPSCOct 25, 2007Nationwide• Jo-Ann Stores Inc., of Hudson, Ohio

PZ50 Snowmobiles (Yamaha) – Steering Danger (2007)

This recall involves all model year 2007 PZ50 snowmobiles, including PZ50W (Phazer), PZ50FXW (Phazer FX), PZ50GTW (Phazer GT), PZ50MW (Phazer Mountain Lite), and PZ50VTW (Venture Lite) model snowmobiles.

CPSCOct 16, 2007Nationwide• Yamaha Motor Corporation U.S.A., of Cypress, Calif.

Abbott Laboratories Inc.: Abbott Clinical Chemistry Creatine Kinase, Model LN 7D63-...

Three potential issues with Creatine Kinase Lot Number: 52044HW00: (1) Decrease in quality control and/or patient results (2) An iIncreased imprecision, or (3) Error Code 1054 (Unable to calculate results, Reaction Failure) on Architect cSystems.

FDAOct 12, 2007Nationwide• Abbott Laboratories Inc.

Abbott Laboratories, Inc: Abbott ACCELERATOR APS System Input/Output Module (IOM); ...

Sample problems; Five issues identified related to software utilized by the ACCELERATOR APS System Input/Output Module, to include: Under three specific conditions, the post-aspiration radio-frequency identification (RF ID) read of the tube carrier is not performed and the APS work cell may not appropriately generate Sample Presentation/Sample Queue errors with APS software version 1.1.1 or earlie

FDAOct 10, 2007Nationwide• Abbott Laboratories, Inc

Abbott Laboratories: Abbott AxSYM AUSAB Reagent Pack, List No: 3C74-20, 100 te...

Incorrect results: Reagents in these lots were manufactured with an incorrect ratio of 2 key components, which could result in both false reactive and false nonreactive specimens.

FDAOct 1, 2007Nationwide• Abbott Laboratories

Abbott Laboratories, Inc: Clinical Chemistry ICT Calibrator, List Number: 1E46-02, ...

Quality Control (Out of Range)- ICT Calibrator lot number: 0505017, may contain an interferent. Not all vials within a kit are affected. The investigation determined that the interferent affects Potassium (K+) only. Use of the affected calibrator vials will generate an acceptable, but low calibration slope. When Quality Control (QC) is run to verify the calibration, K+ QC results may be bel

FDASep 26, 2007PR• Abbott Laboratories, Inc

Bio-Rad Labroatories Inc.: BioPlex 2200 System, Cat. No. 665-1460A containing APF CD...

Mislabeling: Reporting terminology in the Syphilis IgG APF CD is not consistent with the distributed Instructions for Use. (Non-Reactive and Reactive rather than Negative and Positive)

FDASep 25, 2007Nationwide• Bio-Rad Labroatories Inc.

Abbott Laboratories: ARCHITECT i System Assay CD-ROM - WW (excluding USA accou...

The lower limit flag for auto-dilution protocol 3 (amniotic fluid) was set too low (15 ng/mL) for the ARCHITECT AFP assay file for the ARCHITECT AFP non-U.S. product. The assay labeling indicates that the limit flag should be set no lower than 20 ng/mL

FDASep 18, 2007Nationwide• Abbott Laboratories

BD Diagnostic Systems Lee Laboratories: BD DifcoTM Neisseria Meningitidis Antisera Group Y, 2288...

Exhibits cross reactivity with Neisseria meningitides Group W135.

FDASep 6, 2007Nationwide• BD Diagnostic Systems Lee Laboratories

Bio-Rad Laboratories: Bio-Rad Laboratories-MONOLISA Anti-HBc IGM EIA kit, an in...

Incorrect Instruction: the package insert states to add 100L of conjugate; it should state to add 100uL.

FDASep 5, 2007Nationwide• Bio-Rad Laboratories

Abbott Laboratories, Inc: ARCHITECT c16000 Processing Module, for In Vitro Diagnost...

Incorrect Sample/Test Identification: Due to a software timing defect with certain versions of ARCHITECT cSystem Software, test results may be incorrectly associated to a Sample Identification during specific sample-processing conditions of the Robotic Sample Handler.

FDASep 5, 2007PR• Abbott Laboratories, Inc

Abbott Laboratories, Inc: ARCHITECT c8000 Processing Module, for In Vitro Diagnosti...

FDASep 5, 2007PR• Abbott Laboratories, Inc

Karl Storz Endoscopy America Inc 600 Corporate Pointe: Storz Equipment, Fluid Management Stand, for Fluid Manage...

Outflow Difference: The accuracy of the Equimat displayed value could be influenced by external factors of the cart/stand and may result in a fluctuating or inaccurate reading.

FDAAug 17, 2007Nationwide• Karl Storz Endoscopy America Inc 600 Corporate Pointe