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Fitness Quest Inc., of Canton, Ohio

Fitness Quest Inc., of Canton, Ohio Recalls

All product recalls associated with Fitness Quest Inc., of Canton, Ohio.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

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 34581–34600 of 37665 recalls

Gazelle Freestyle Cross Trainer (Fitness Quest) – Fall Hazard (2006)

Gazelle® Freestyle Crosstrainer and Crosstrainer Pro exercisers are "glider-style" exercise equipment. The user moves two foot platforms in a striding motion back and forth while grasping handlebars attached to the platforms. The model name "Gazelle Freestyle Cross Trainer" or "Gazelle Freestyle Cross Trainer Pro" is printed on the side of each product's frame.

CPSCJun 7, 2006Nationwide• Fitness Quest Inc., of Canton, Ohio

ArthroCare Corporation: ArthroCare brand OPUS Smartstitch Suture Cartridge, Catal...

Potential loss of product sterility due to breach of pouch seal.

FDAJun 7, 2006Nationwide• ArthroCare Corporation

Pointe Scientific, Inc.: Glucose HEX R2 reagent sold by Pointe Scientific; in vitr...

Product does not meet performance specifications through its labeled expiration period.

1...1728 172917301731 1732...1884

Page 1730 of 1884Next

FDA

Jun 7, 2006

Nationwide

• Pointe Scientific, Inc.

Endurance Treadmills (Joong Chen) – Unexpected Speed Changes (2006)

The recall includes the T7, T7.1, T8 and T9.1 models of the Endurance Treadmills. The treadmills are black and silver. The model number is located along the side of the running surface near the end of the treadmill. Consumers should check the serial number, located on the front lower shroud of the treadmill along the vertical surface on a white sticker, and contact the company to confirm their treadmill is included in the recall.

CPSCJun 7, 2006Nationwide• Joong Chen Industries, of Taiwan

Pointe Scientific, Inc.: Glucose Hex reagent, sold by Pointe Scientific; in vitro ...

Product does not meet performance specifications through its labeled expiration period.

FDAJun 7, 2006Nationwide• Pointe Scientific, Inc.

Pointe Scientific, Inc.: Pointe Scientific Liquid Glucose HEX (R1) Reagent Set, fo...

Product does not meet performance specifications through its labeled expiration period.

FDAJun 7, 2006Nationwide• Pointe Scientific, Inc.

Pointe Scientific, Inc.: Glucose HEX R1 reagent sold by Pointe Scientific; in vitr...

Product does not meet performance specifications through its labeled expiration period.

FDAJun 7, 2006Nationwide• Pointe Scientific, Inc.

GE Healthcare: GE Innova 2100-IQ Digital Fluoroscopic Imaging System, Ve...

The systems do not contain a certification label on the C2 Cabinet (Beam-limiting control).

FDAJun 6, 2006AL, AZ, AR +27 more• GE Healthcare

Radiometer America Inc: Qualicheck 1+, Aqueous Quality Control, Level 2, S7140, R...

The barcode for the ABL77 on the insert incorrectly enters a control range for pH of 7.90-7.95 into the analyzer. The insert correctly states that the control range is 7.40-7.45.

FDAJun 6, 2006KY, NY, NC• Radiometer America Inc

Abbott Laboratories MPG: ARCHITECT Ferritin Reagent; in vitro diagnostic; list num...

Some ARCHITECT Ferritin Reagent lots may not be meeting the accuracy by correlation to AxSYM claims as they are listed in the package insert (slope of 1.0 +/- 0.2).

FDAJun 6, 2006Nationwide• Abbott Laboratories MPG

St. Francis Medical Technologies Inc: St. Francis Medical Technologies brand X STOP Interspinou...

Some units may be mislabeled as 10 mm X STOP implant that actually contain 14 mm X STOP implant.

FDAJun 6, 2006Nationwide• St. Francis Medical Technologies Inc

Radiometer America Inc: Qualicheck 1+, Aqueous Quality Control, Level 2, S7140, R...

The barcode for the ABL77 on the insert incorrectly enters a control range for pH of 7.90-7.95 into the analyzer. The insert correctly states that the control range is 7.40-7.45.

Class IIILow

FDAJun 6, 2006KY, NY, NC• Radiometer America Inc

Medtronic Neuromodulation: Medtronic SynchroMed EL Programmable Pumps, Models 8627-1...

The Catheter Access Port (CAP) on SynchroMed EL pumps manufactured between March and July 1999 may detach from the main body of the pump, which can interrupt drug flow to the target site.

FDAJun 6, 2006Nationwide• Medtronic Neuromodulation

Varian Medical Systems Inc: Varian brand Clinac C-series Pendant Radiation delivery s...

Machine may produce unexpected motions from the couch, collimator, and gantry rotation at maximum speeds.

FDAJun 6, 2006Nationwide• Varian Medical Systems Inc

Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany: ExacTrac Robotics, sold alone as Robotic Tilt Module cata...

During ExacTrac Robotics installation on the Varian Exact Couch, the couch height position indication is re-calibrated to read out the correct positions. This re-calibration could cause the eventual failure of the vertical lift mechanism of the couch, which might result in patient injury or death.

FDAJun 2, 2006Nationwide• Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany

Boston Scientific Corp: Boston Scientific Vesica Sling Kits with Drill-In Anchor ...

The packages are labeled sterile, but the product was not sterilized.

FDAJun 2, 2006Nationwide• Boston Scientific Corp

Boston Scientific Corp: Boston Scientific Vesica Drill-In Bone Locator; sterile, ...

The packages are labeled sterile, but the product was not sterilized.

FDAJun 2, 2006Nationwide• Boston Scientific Corp

Biogenex Laboratories: BioGenex brand Hepatitis B Virus Core Antigen Antibody, C...

Misbranding-The product labeling (label and insert) is misbranded in that the product does not comply with the labeling requirements for an Analyte Specific Reagent (ASR).

FDAJun 2, 2006Nationwide• Biogenex Laboratories

Stryker Endoscopy: Stryker brand Insufflation Tube Set and High Flow Insuffl...

Device for which sterility may be compromised as evidenced by a loss of package integrity.

FDAJun 2, 2006Nationwide• Stryker Endoscopy

Nexgrill Gas Grill (Nexgrill) – Fire Hazard (2006)

Fire/Burn Risk

The recalled product is the Nexgrill Model 720-0025 Gas Grill. The stainless steel grill is designed to be used with propane gas. The name of the grill is located at the left corner of the exterior of the main burner lid. The serial number is printed on the CSA sticker, which is located behind the door. A temperature gauge is located at the center of the main burner lid.

CPSCJun 1, 2006Nationwide• Nexgrill Industries Inc., of City of Industry, Calif.