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OTT-LITE Technology of Tampa, Florida

OTT-LITE Technology of Tampa, Florida Recalls

All product recalls associated with OTT-LITE Technology of Tampa, Florida.

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Recall Summary

Total Recalls

1000

Past Year

899

Class I (Serious)

125

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 16941–16960 of 17592 recalls

10,000 Lux Light Box (OTT-LITE) – Safety Concern (2004)

Fire/Burn Risk

The recalled "10,000 Lux Light Box" produces light to simulate natural sunlight. The units, which are white with a translucent hinged door, measure 24 inches high, 12 ½ inches wide, and 3 ¾ inches deep. Some of the recalled light boxes may have a small label on the top of the unit with the name "Nu-Yu Light." Only the "10,000 Lux Light Box" sold by Natural Options is recalled.

CPSCAug 11, 2004Nationwide• OTT-LITE Technology of Tampa, Florida

Conmed Corporation: ConMed Stealth Coated Laparoscopic Electrodes with 3/32''...

Insulation may pull away from the hub of the electrode exposing the conductive shaft below. This condition results in potential for electrical shock.

FDAAug 9, 2004IN• Conmed Corporation

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...

1...846 847848849 850...880

Page 848 of 880Next

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

Peek-a-Boo Ball (HearthSong) – Child Safety (2004)

Choking Hazard

The recalled toy is a blue wooden ball with six holes located equally around the ball. Each hole contains a small wooden head with a smiling face in various colors.

CPSCAug 6, 2004Nationwide• HearthSong Inc., of Madison, Va.

Rival Crock-Pot Slow Cooker (Holmes Group) – Manufacturing Defect (2004)

Fire/Burn Risk

Only Rival Crock-Pot® slow cookers with model numbers 3040, 3735, 5025, 5070 and 5445 manufactured before May 2002 are included in the recall. The model number is printed on the UL label located on the bottom of the base. The recalled Rival slow cooker has a removable ceramic bowl that sits inside of a metal base. The Rival logo is printed on the front of the unit above the control knob. The bases are round or oval in shape and were sold in various colors and designs. A date code is stamped onto the plug at the end of the power cord attached to each unit. The first two digits represent the week of manufacture, and the last two digits represent the year of manufacture. Any plug with a date code from 0199 (1st week of 1999) to 1802 (18th week of 2002) is included in this recall.

CPSCAug 5, 2004Nationwide• The Holmes Group Inc., of Milford, Mass.

Medibo N.V. Heikant 5 Hanmont, Achel Belgium: Minerva Patient Lift, model ML-20; this lift has a passiv...

The hanger bar may detach from the jib yoke, the M8 bolt in the foot pedal assembly may come loose, and some units may have faulty actuator brackets on the mast assembly, resulting in the patient lift becoming unstable and allowing the patient to fall.

FDAAug 4, 2004CA, FL, LA +7 more• Medibo N.V. Heikant 5 Hanmont, Achel Belgium

B10 Décor Light Bulbs (Osram Sylvania) – Electrical Hazard (2004)

Fire/Burn Risk

The recalled 60-watt B10 medium base light bulbs were sold in packages of two or four units. The bulbs are clear. Some were packaged as "Ceiling Fan" and "Double Life" light bulbs. "SYLVANIA" is printed on the front of the packaging and on the bulb base. The bulbs involved have a UPC bar code on the back of the package, ending in the following five digits: 13323, 13329, 13333, 13442, 13445, 13454, 13565, 13650, and 13721.

CPSCAug 4, 2004Nationwide• Osram Sylvania Products Inc., of Danvers, Mass.

Portable Electric Heaters (Vornado) – Safety Malfunction (2004)

Fire/Burn Risk

The recalled portable electric whole-room heaters are designed for indoor use and have model numbers 180VH®, VH®, Intellitemp®, EVH®, and DVH®. The model numbers are located on the bottom of each unit. Each heater is about 11-1/2 inches long, 9-1/2 inches wide, and about 12 inches tall; weighs about 6 lbs.; and has the "Vornado" name and symbol on the front.

CPSCAug 3, 2004Nationwide• Vornado Air Circulation Systems Inc., of Andover, Kan.

Beckman Coulter Inc: CXP Software Version 1.0 and 1.1 (operating software for ...

Software anomaly.

FDAAug 2, 2004Nationwide• Beckman Coulter Inc

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

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

Beckman Coulter Inc: Synchron Systems Hemoglobin A1c (HbA1c) Reagent

Results of tests are biased low due to a vendor change in formulation not brought to the attention of the recalling firm.

FDAJul 30, 2004Nationwide• Beckman Coulter Inc

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

Beckman Coulter Inc: SYNCHRON Clinical Systems Enzyme Validator Kit

incorrect Calibration Acceptance Limits.

FDAJul 29, 2004Nationwide• Beckman Coulter Inc

Eyelash Curlers (W.E. Bassett) – Design Flaw (2004)

The "Frosted Grip" eyelash curlers have pink-plastic handles and are sold with a rubber re-fill pad. The eyelash curlers were sold under various brand names, including TRIM and Salon Plus. There are no identifying marks on the eyelash curler. However, item numbers are printed on the packaging. Item numbers involved in the recall include 5-87B (sold at Wal-Mart, CVS and Shopko), 5-87RA (sold at Rite Aid) and 5-87S (sold at Kroger).

CPSCJul 29, 2004Nationwide• The W.E. Bassett Company, of Shelton, Conn.

Greiner VACUETTE North America: Greiner bio-one, VACUETTE TUBE, 9NC Coagulation Citrate 3...

Coagulation tubes may not have received the proper fill of citrate solution.

FDAJul 27, 2004Nationwide• Greiner VACUETTE North America

Dade Behring Inc. Rte 896, Glasgow Business Community: BC Thrombin Reagent . Thrombin Time Test

The product does not demonstrate the expected prolonged thrombin times for specimens obtained from patients recieving heparin

FDAJul 21, 2004CT, FL, IL +5 more• Dade Behring Inc. Rte 896, Glasgow Business Community

Philips Medical Systems Sales & Service Region No. America: BV212 Mobile X-Ray System

Potential for c-arm to move due to loose screws

FDAJul 20, 2004Nationwide• Philips Medical Systems Sales & Service Region No. America

Philips Medical Systems Sales & Service Region No. America: BV29 Mobile X-Ray System

Potential for c-arm to move due to loose screws

FDAJul 20, 2004Nationwide• Philips Medical Systems Sales & Service Region No. America