Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Nichols Institute Diagnostics

Nichols Institute Diagnostics Recalls

All product recalls associated with Nichols Institute Diagnostics.

Get alerts for this brand

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 20121–20140 of 21319 recalls

Nichols Institute Diagnostics: Nichols Advantage ACTH Test System, catalog number 62-7004.

Performance does not meet claims in the Directional Insert concerning correlation with the IRMA ACTH assay.

FDAApr 22, 2005Nationwide• Nichols Institute Diagnostics

International Biophysics Corp: IBC FloProbe (Non-sterile), a disposable flow probe that ...

Complaints received regarding the device's failure to zero out.

FDAApr 22, 2005Nationwide• International Biophysics Corp

Sharp CRT Television – Tube Model Defect (2005)

Fire/Burn Risk

The recalled 27-inch Sharp conventional tube televisions include models 27RS50, 27RS100 and CSR5027. The model number can be found on the label on the back of the television.

1...1005 100610071008 1009...1066

Page 1007 of 1066Next

CPSC

Apr 21, 2005

Nationwide

• Sharp Electronics Corp., of Mahwah, N.J.

Boston Scientific Scimed: PTFE (Polytetrafluoroethylene) felt. Catalog #s: M00200...

Units of these lots may have areas of lower density resulting in lower tensile and suture retention strength.

FDAApr 19, 2005Nationwide• Boston Scientific Scimed

Becton Dickinson & Company: BD #11 Bard Parker Scalpel. A general use surgical blade...

A small percentage of scalpels exhibited a 'double blade' condition.

FDAApr 19, 2005IL, IN, TN +4 more• Becton Dickinson & Company

Smiths Medical ASD, Inc.: Bivona brand Cuffless Extra Length Fixed Hyperflex Adult ...

The shaft was manufactured approximately 1 to 3 mm under the length specification, and may be 105 mm in length.

FDAApr 19, 2005CA, IN, NC• Smiths Medical ASD, Inc.

Roche Diagnostics Corp.: Roche brand AccuData GTS/GTS Plus System Replacement Base...

If foil wrapped packages or other metallic objects are lodged behind the supply drawer, an electrical short may result and high heat generated; this could result in plastic melting and battery leakage for customers using 'C' cell batteries to power their base and could render the system inoperable (system won't turn on) for customers using the A/C adaptor without batteries.

FDAApr 18, 2005Nationwide• Roche Diagnostics Corp.

Roche Diagnostics Corp.: Roche brand AccuData GTS Plus System; Catalog number 3000...

FDAApr 18, 2005Nationwide• Roche Diagnostics Corp.

Ortho-Clinical Diagnostics: VITROS VALP Reagent , REF 680 1710. Each box contains 6 ...

Negatively biased results may be observed when the reagent is stored on the VITROS 5,1FS Chemistry System for less than seven days.

FDAApr 18, 2005Nationwide• Ortho-Clinical Diagnostics

Roche Diagnostics Corp.: Roche brand AccuData GTS System; Catalog number 404, mate...

FDAApr 18, 2005Nationwide• Roche Diagnostics Corp.

Stryker Howmedica Osteonics Corp.: Xcelerate Patella System Reamer Shaft Assembly; Non-Steri...

The Xcelerate Patella Reamer Shaft Assembly and the Reamer Adapter do not mate properly. This could result in the removal of excessive bone from the patella leading to a thinner patella; a patella that does not have enough bone for adequate engagement with pegs or patella fracture.

FDAApr 15, 2005Nationwide• Stryker Howmedica Osteonics Corp.

Nichols Institute Diagnostics: Nichols Advantage QuiCk- Intraoperative Bio-Intact PTH As...

Controls were out of specification range.

FDAApr 14, 2005Nationwide• Nichols Institute Diagnostics

Honda FourTrax ATVs (American Honda) – Potential Safety Issue (2005)

The recall includes 2004-2005 FourTrax Honda ATVs. The ATVs are red, olive, yellow or blue and have "Honda" written on the fuel tank. The following models are included in recall: Year Model No. Model Name VIN Range 2004 TRX350TE Rancher ES 478TE244*44300003 through 478TE244*44310382 TRX350TM Rancher 478TE240*44300006 through 478TE240*44310445 TRX350FE Rancher 4x4 ES 478TE254*44300010 through 478TE254*44323289 TRX350FM Rancher 4X4 478TE250*44300005 through 478TE250*44315544 TRX400FA Rancher AT 478TE290*44000055 through 478TE290*44019249 TRX400FGA Rancher AT GPS 478TE294*44000016 through 478TE294*44008055 2005 TRX250TE Recon ES 1HFTE214*54500014 through 1HFTE214*54510334 TRX250TM Recon 1HFTE210*54500010 through 1HFTE210*54509249 TRX350TE Rancher ES 1HFTE244*54400001 through 1HFTE244*54412240 TRX350TM Rancher 1HFTE240*54400001 through 1HFTE240*54410980 TRX350FE Rancher 4x4 ES 1HFTE254*54400001 through 1HFTE254*54415180 TRX350FM Rancher 4x4 1HFTE250*54400001 through 1HFTE250*54416860 TRX400FA Rancher AT 1HFTE290*54100005 through 1HFTE290*54115657 TRX400FGA Rancher AT GPS 1HFTE294*54100004 through 1HFTE294*54103423 TRX500TM Foreman 1HFTE314*54000012 through 1HFTE314*54002112 TRX500FM Foreman 4x4 1HFTE310*54000015 through 1HFTE310*54002715 TRX500FE Foreman 4x4 ES 1HFTE317*54000026 through 1HFTE317*54003486 TRX500FA Foreman Rubicon 1HFTE260*54400010 through 1HFTE260*54402169 TRX500FGA Foreman Rubicon GPS 1HFTE264*54400012 through 1HFTE264*54400555 TRX650FA Rincon 4x4 1HFTE280*54000009 through 1HFTE280*54011239 TRX650FGA Rincon 4x4 GPS 1HFTE284*54000002 through 1HFTE284*54002521 The model numbers can be found on the identification label located on the left side of the frame down tube. The VIN number is stamped on the front side of the frame.

CPSCApr 14, 2005Nationwide• American Honda Motor Co. Inc., of Torrance, Calif.

Varian Medical Systems: Flexible Implant tube, blind end, 350 mm, part # GM110037...

A defective treatment applicator in a cancer therapy medical device may become separated potentially causing patient injury.

FDAApr 14, 2005CO, CT, IN +4 more• Varian Medical Systems

Diagnostica Stago, Inc.: PTT-LA. Lupus anticoagulant-sensitive APTT reagent. Dia...

Variable clotting times observed with the PTT-LA, Lupus Anticoagulant-Sensitive APTT Reagent.

FDAApr 13, 2005Nationwide• Diagnostica Stago, Inc.

Leica Microsystems, Inc.: Leica M520 Surgical Microscope; a surgical microscope wit...

Fire/Burn Risk

Patient Burns-The use of the surgical microscope at high light intensity and short working distances can result in patient burns.

FDAApr 12, 2005Nationwide• Leica Microsystems, Inc.

Hitachi Medical Systems America Inc: Altaire, Magnetic Resonance Imaging Device.

Fire/Burn Risk

The electrical cables that supply gradient power to the magnet can become loose over time and create a potential fire hazard.

FDAApr 11, 2005AL, AZ, AR +34 more• Hitachi Medical Systems America Inc

Northwest Medical Physics Equipment Inc: ISOLOC Software Version 6.0, Localization software for de...

When ISOLOC version 6.0 was used in the centimeter mode, the display in the couch moves window had a rounding error relative to the Portal Image Marker window of up to 0.5 mm.

FDAApr 11, 2005Nationwide• Northwest Medical Physics Equipment Inc

Siemens Medical Solutions USA, Inc: Axiom Artis X-Ray System using software version VB11D or ...

Live display in exam room may sporadically stop working although the display in the control room remains fully operational

FDAApr 11, 2005AL, AZ, AR +34 more• Siemens Medical Solutions USA, Inc

Nichols Institute Diagnostics: Bio-Intact PTH (1-84) Assay, Catalog No. 62-7040

Values do not agree with Directional Instructions.

FDAApr 7, 2005Nationwide• Nichols Institute Diagnostics