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Cybex International, Inc., of Medway, Mass.

Cybex International, Inc., of Medway, Mass. Recalls

All product recalls associated with Cybex International, Inc., of Medway, Mass..

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

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 22981–23000 of 25000 recalls

Treadmills (Cybex) – Fire Hazard (2007)

Fire/Burn Risk

This recall involves the treadmills "Cybex 400T," "Cybex 410T," "Trotter 510," "Trotter 525", "Trotter 535", and "CXT+" that were recalled on October 8, 2003 and later repaired. The treadmills are black with gray coloring, have rectangular uprights, and measure 69 inches long and 30 inches wide. The brands and models are written on the display panel. The "CXT+" model does not bear the brand Cybex or Trotter.

CPSCOct 23, 2007Nationwide• Cybex International, Inc., of Medway, Mass.

Hydration Unit Power Packs (Collegiate Pacific) – Injury Risk (2007)

This recall involves the battery-operated power pack boxes for the 20-gallon "Sports Cool Powered Team Drinker" and the 40-gallon "Sports Cool Powered Tanker with Cart" portable team hydration units. The units include a water tank, six hoses, a battery-operated pack box, and a cart. "Sports Cool" is printed on the water tank.

CPSCOct 22, 2007Nationwide• Collegiate Pacific, of Farmers Branch, Texas

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GE OEC Medical Systems, Inc: GEHC OEC 8800 Mobile Fluoroscopic X-ray System, GE Health...

X-ray units did not meet manufacturer's specification for linearity.

FDAOct 19, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: GEHC OEC 8800 Mobile Fluoroscopic X-ray System, GE Health...

X-ray units did not meet manufacturer's specification for linearity.

Class IIModerate

FDAOct 19, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: GE OEC, Insta Trak 3500 Plus with the Cranial Application...

Crack, Fracture or Detachment: The Transmitter Arm for the Mayfield-compatible Transmitter may become detached from the unit and enter into the surgical field.

FDAOct 18, 2007AL, AZ, AR +22 more• GE OEC Medical Systems, Inc

Ladder Stands (Gorilla) – Fall Hazard (2007)

This recall involves Gorilla Kong Maxx Ladder Stands with model number 43032 and batch numbers G051507, G051507D, G061507D, G071507D, and G081507D. Model numbers are printed on the box only. Batch numbers are stamped on the vertical rail of the first ladder section. The stand is 19 feet to the shooting rail, or 16 feet 8 inches to the platform. The foot platform measures 17½ inches wide. This is the only Gorilla, Inc. ladder stand with these dimensions.

CPSCOct 18, 2007Nationwide• Gorilla Inc., of Flushing, Mich.

John Deere Gator Vehicles – Injury Risk (2007)

This recall involves the XUV and HPX Gator utility vehicles made by John Deere with model and serial numbers included below. These are four-wheeled vehicles with a cargo box. "John Deere", "Gator", "HPX" and "XUV" are printed on the side of the cargo box. The following model and serial numbers can be found on the serial number plate on the frame of the vehicle: Model Serial Number XUV 620i Gas MOXUVGX013294-016669 XUV 620i Gas MOXUVGT011480-012186 XUV 850D Diesel MOXUVDX011917-013329 XUV 850D Diesel MOXUVDT010001-010449 HPX 4X4 Diesel MOHP4DX050877-051453 HPX 4X4 Gas MOHP4GX051221-052763

CPSCOct 17, 2007Nationwide• Deere & Company, of Moline, Ill.

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.

PML, Inc. dba Pml Microbiologicals Inc.: PML --IDS Rapid NH QC Set- Quality Control kit for cultur...

Incorrect micro-organism-- .Quality control In-vitro diagnostic test was manufactured with Cryptococcus neoformans (ATCC 76484) instead of Haemophilus parainfluenzae (ATCC 7901).

FDAOct 15, 2007Nationwide• PML, Inc. dba Pml Microbiologicals Inc.

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Sprint Fidelis 6948 Steroid eluting, quadripola...

Medtronic Cardiac Rhythm Disease Management has voluntarily suspended worldwide distribution of the Sprint Fidelis family of defibrillation leads because of the potential for lead fractures. In addition, the company recommends against new implants of the leads (Sprint Fidelis Models: 6930, 6931, 6948, 6949). Medtronic, its Independent Physician Quality Panel, and Bruce Lindsay, M.D., Professor of

FDAOct 15, 2007PR• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Sprint Fidelis 6930 Steroid eluting, tripolar, ...

FDAOct 15, 2007PR• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Sprint Fidelis 6931 Steroid eluting, tripolar, ...

FDAOct 15, 2007PR• Medtronic Inc. Cardiac Rhythm Managment

PML, Inc. dba Pml Microbiologicals Inc.: PML -- LyfoCults Haemophilus parainfluenzae - micro organ...

Incorrect micro-organism-- Quality control In-vitro diagnostic test was manufactured with Cryptococcus neoformans (ATCC 76484) instead of Haemophilus parainfluenzae (ATCC 7901).

FDAOct 15, 2007Nationwide• PML, Inc. dba Pml Microbiologicals Inc.

Haemonetics Corporation: Haemonetics cardioPAT System, Product List Number 02050, ...

Labeling (additional) use instructions: to clarify proper position of cardioPAT device and post-op line to prevent fluid build up from patient's chest

FDAOct 15, 2007Nationwide• Haemonetics Corporation

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Sprint Fidelis 6949 Steroid eluting, quadripola...

FDAOct 15, 2007PR• Medtronic Inc. Cardiac Rhythm Managment

PML, Inc. dba Pml Microbiologicals Inc.: PML -- Vitek NH ID Card (NHI) Set - Quality Control kit ...

Incorrect micro-organism-- .Quality control In-vitro diagnostic test was manufactured with Cryptococcus neoformans (ATCC 76484) instead of Haemophilus parainfluenzae (ATCC 7901).

FDAOct 15, 2007Nationwide• PML, Inc. dba Pml Microbiologicals Inc.

Gas Regulators (Fisher Controls) – Leak Hazard (2007)

Fire/Burn Risk

The recalled gas regulators were manufactured from March 2007 through May 2007 and installed on natural gas or LP-gas supply systems in homes and small commercial buildings. The recalls involves model HSR natural gas regulators and LP-gas regulators with model numbers 67CD, 67CH, 67CN, and 67CW, HSRL, R622, R622E, R622H, R632, R642, R652, R652E, R122H, R222, or R232. The model number can be found on a white label attached to the regulator spring case. The date of manufacture is also stamped on the regulator.

CPSCOct 12, 2007Nationwide• Fisher Controls International (FCI), of McKinney, Texas

Aesculap Implant Systems: Excia Cemented Hip Stems, Size 9mm, Part Number: NJ309K, ...

Sterility (package integrity) Compromised: Device package damaged during shipment

FDAOct 10, 2007Nationwide• Aesculap Implant Systems

AmniSure International LLC: AmniSure ROM Test, Fetal Membrane Rupture Test for In-Vi...

Weak true postive/false negative results: weak true positive or false negatives in ruptured fetal membranes may occur due to a "hook effect"

FDAOct 3, 2007Nationwide• AmniSure International LLC

Acist Medical Systems: ACIST Multi-Use Syringe Kit, Model A2000; SKU # : 014612;...

Syringe Fracture: the syringe may be fractured, causing contrast to be sprayed from syringe fracture.

FDAOct 3, 2007Nationwide• Acist Medical Systems