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Louisville Apl Diagnostics Inc

Louisville Apl Diagnostics Inc Recalls

All product recalls associated with Louisville Apl Diagnostics Inc.

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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 20481–20500 of 21319 recalls

Louisville Apl Diagnostics Inc: american diagnostica inc. IgM Conjugate, 15mL; component ...

Product mislabeled; conjugate IgG placed in bottles labeled as conjugate IgM and vice versa.

FDAAug 10, 2004CT, IN• Louisville Apl Diagnostics Inc

Siemens Medical Solutions USA, Inc: Axiom Artis BA or BC Biplane System, Angiographic x-ray s...

Opacification Function of device may incorrectly merge images

FDAAug 10, 2004Nationwide• Siemens Medical Solutions USA, Inc

U & I America: Optima Spinal System and Spinal Hook System, set screw co...

Threads on a set screw, as a component of a spinal fixation system, may break off during use.

FDAAug 10, 2004CA• U & I America

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Louisville Apl Diagnostics Inc: american diagnostica inc. IgG Conjugate, 15mL; component ...

Product mislabeled; conjugate IgG placed in bottles labeled as conjugate IgM and vice versa.

FDAAug 10, 2004CT, IN• Louisville Apl Diagnostics Inc

Boston Scientific Corporation: Manual Biopsy Devices containing AIM system: Chiba Needl...

Incomplete graduation on the needle guard, which would cause the graduations to be off by as much as 1 cm.

FDAAug 9, 2004Nationwide• Boston Scientific Corporation

Roche Diagnostics Corp.: MagNA Pure LC Instrument; catalog numbers 2236931 and 036...

A hardware/software problem will result in low elution volumes and bias sample results for various protocols.

FDAAug 6, 2004Nationwide• Roche Diagnostics Corp.

Roche Diagnostics Corp.: Roche/Hitachi 747 - 100 clinical chemistry analyzer; cata...

A software defect will allow the reporting out of believable, but clinically significant, erroneous results if the analyzer is in operation and a channel has been masked or not requested over a period of time.

FDAAug 6, 2004Nationwide• Roche Diagnostics Corp.

Roche Diagnostics Corp.: Roche/Hitachi 747 - 200 clinical chemistry analyzer; cata...

A software defect will allow the reporting out of believable, but clinically significant, erroneous results under certain conditions.

FDAAug 6, 2004Nationwide• Roche Diagnostics Corp.

Omrix Biopharmaceuticals, Ltd. Plasma Fract. Inst. Magen David Adom Blood Services Ctr., Sheba Hospital Ramat Gan Israel: Crosseal, fibrin sealant (human), This package***, One Ap...

5 mL Crosseal fibrin sealant (human) is difficult to expel from the device resulting in product leakage from the vial insertion port .

FDAAug 6, 2004Nationwide• Omrix Biopharmaceuticals, Ltd. Plasma Fract. Inst. Magen David Adom Blood Services Ctr., Sheba Hospital Ramat Gan Israel

Roche Diagnostics Corp.: Roche/Hitachi Modular Additional D Module DAT clinical ch...

A software defect will allow the reporting out of believable, but clinically significant, erroneous results under certain conditions.

FDAAug 6, 2004Nationwide• Roche Diagnostics Corp.

Roche Diagnostics Corp.: Roche/Hitachi Modular Analytical D Module clinical chemis...

A software defect will allow the reporting out of believable, but clinically significant, erroneous results under certain conditions.

FDAAug 6, 2004Nationwide• Roche Diagnostics Corp.

St. Jude Medical/Daig Division: Telesheath Left Atrial Introducer System Right Superior. ...

St. Jude Medical received two complaints from customers involving the Telesheath Left Atrial Introducer System side arm detaching from the hub of the inner sheath. Subsequent testing of Telesheath inventory at St. Jude Medical indicated that the side arm from the inner sheath can detach during routine handling and manipulation, and occurs on a random basis.

FDAAug 4, 2004Nationwide• St. Jude Medical/Daig Division

Philips Medical Systems (Cleveland) Inc: Extended Brilliance Workspace Imaging Workstation. An ind...

Due to a software deficiency that occurs in the combine mode, a patients image can be filmed over a different patients image.

FDAAug 2, 2004Nationwide• Philips Medical Systems (Cleveland) Inc

Zoll Medical Corporation: Zoll M Series Automated Defibrillator (AED)

Visual Sreen display and audible prompt may not advise to 'Press Shock'

FDAAug 2, 2004Nationwide• Zoll Medical Corporation

General Electric Med Systems: SMV FX-80 Nuclear Camera

The detector head of a FX-80 Nuclear camera may fall from the gantry. Three potential causes have been determined. (1) A ball nut in the detector's radial drive assembly can back out of the bearing block that contains it. (2) Misalignment of the radial drive assembly. (3) Mounting bolts on the radial drive assembly may become loose, fail, or back out.

FDAJul 30, 2004Nationwide• General Electric Med Systems

General Electric Med Systems: SMV FX-40 Nuclear Camera

FDAJul 30, 2004Nationwide• General Electric Med Systems

TV/VCR Combination (Matsushita) – Ventilation Issue (2004)

The recalled combination TV/VCRs are gray/black and have these brand names: Panasonic, Quasar, RCA, or JCPenney. The cabinets have ventilation holes in the top rear of the cabinet. Only the 13" and 20" Combination TV/VCR sets manufactured between January 1, 1995, and December 30, 1995, are recalled. These sets can be identified by the model number which appears on the front and rear of the cabinet. The following model numbers are included in this recall: Brand Model Panasonic 13-inch models: PV-M1325, PV-M1345, PVM1365AD, AG-513B 20-inch models: PV-M2025, PV-M2035, PV-M2045, PV-M2065, AG-520B Quasar 13-inch model: VV-1305 20-inch models: VV-2005T, VV-2005, VV-2025 Thomson (RCA) 13-inch models: T13015BC, T13018BC 20-inch models: T20015BC, T20018BC, T20020BC JCPenney 20-inch model: 685-0879

CPSCJul 30, 2004Nationwide• Matsushita Electric Corporation of America, Secaucus, New Jersey

Siemens Medical Solutions USA, Inc: Magnetom Harmony MRI System Model number 7106714

An input error can be made with Magnetom MRI software. Software allows users to manually change Transmit Reference Voltage in certain windows

FDAJul 28, 2004CA, CO, CT +19 more• Siemens Medical Solutions USA, Inc

Siemens Medical Solutions USA, Inc: Magnetom Sonata MRI System, Model 7388148

An input error can be made with Magnetom MRI software. Software allows users to manually change Transmit Reference Voltage in certain windows

FDAJul 28, 2004CA, CO, CT +19 more• Siemens Medical Solutions USA, Inc

Siemens Medical Solutions USA, Inc: Magnetom Avanto MRI System, Model 7391167

An input error can be made with Magnetom MRI software. Software allows users to manually change Transmit Reference Voltage in certain windows

FDAJul 28, 2004CA, CO, CT +19 more• Siemens Medical Solutions USA, Inc