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The W.E. Bassett Company, of Shelton, Conn.

The W.E. Bassett Company, of Shelton, Conn. Recalls

All product recalls associated with The W.E. Bassett Company, of Shelton, Conn..

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Recall Summary

Total Recalls

1000

Past Year

567

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 7341–7360 of 7756 recalls

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.

Advanced Bionics Corporation: Auria PowerPak, Model CI-7400-xxx where xxx denotes color...

Fire/Burn Risk

Battery pack may overheat and cause patient burns.

FDAJul 27, 2004Nationwide• Advanced Bionics Corporation

Abbott Laboratories Diagnostic Div: Abbott Clinical Chemistry AEROSET/ ARCHITECT c8000 Creati...

Precipitate formed in product.

1...366 367368369 370...388

Page 368 of 388Next

FDAJul 27, 2004Nationwide• Abbott Laboratories Diagnostic Div

Baxter Healthcare Renal Div: Accura System for Blood Filtration, product codes 5M5660...

The Accura machine display screen may go blank during patient treatment. There is a potential risk to the patient in that the operator may try to manipulate the controls in response to a blank screen, which could affect the current patient's treatment

FDAJul 26, 2004Nationwide• Baxter Healthcare Renal Div

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

Range Hoods (Bosch) – Blower Malfunction (2004)

The recalled range hoods were sold under the "Bosch" brand name and have model numbers DAH93xxUC and DAH94xxUC. The blowers have model numbers DHG4001UC and DHG6001UC. Date codes of the recalled units are 8309 through 8404. The date code appears as the first four digits of the FD number. The Bosch® brand, the model number and FD number can be found on the nameplates. The nameplate of the hood is located on the front side of the back wall of the air channel. The nameplate of the blower is located on at the left side of the housing. If the unit has a green dot by the nameplate, it has already been repaired. The Bosch® name also appears on the front of the hoods. The hoods have black, white or stainless steel finishes.

CPSCJul 20, 2004Nationwide• BSH Home Appliances Corp., of Huntington Beach, Calif.

Boston Scientific Corporation: Express 2 Monorail Coronary Stent Systems (bare metal ste...

Due to characteristics in the delivery catheters that have the potential to impede balloon deflation during a coronary angioplasty procedure.

FDAJul 16, 2004Nationwide• Boston Scientific Corporation

Steel Toe Logger Boots (Georgia Boot) – Safety Concern (2004)

Laceration Risk

The recalled steel toe logger boots are brown and black and have laces that tie up to the calf. The recalled boots have stock numbers of G8320, G8322, and G9360, which can be found on a label under the tongue of the boot. The same label has stitching of the "Georgia Boot" name.

CPSCJul 14, 2004Nationwide• Georgia Boot, of Franklin, Tenn.

Abbott Health Products, Inc.: AxSYM Total B-hCG Reagent Pack

Complaints have been received for AxSYM Total B-hCG Reagents lots 17202Q100, 17556Q100 and 17387Q100 failing calibrations.

FDAJul 7, 2004Nationwide• Abbott Health Products, Inc.

ABX Diagnostics Inc: PENTRA 120 and PENTRA 120 Retic Hematology Analyzer

Power failure having impact on software.

FDAJun 24, 2004Nationwide• ABX Diagnostics Inc

DC Power Supply Units (Basler Electric) – Electrical Safety Issue (2004)

Fire/Burn Risk

These recalled 12-volt DC power supply units were sold as an accessory power supply device for some of Lutron Electronic's wall stations and control interfaces, including some Grafik Eye 3000 lighting control systems. These systems were professionally installed in indoor commercial and residential settings for lighting and dimmer control applications. The power supplies are black plastic with "Basler Electric" and the model number "BE29736001" imprinted on the plug side. On the opposite side is a blue and white Lutron label with the number "GRX-12VDC." Lutron's Grafik Eye 3000 lighting system is not part of the recall.

CPSCJun 15, 2004Nationwide• Basler Electric Co., of Highland, Ill.

Abbott Laboratories HPD/ADD/GPRD: ABBOTT TestPack+Plus Strep A with On Board Controls (OBC)...

False Positive results may be obtained with the identified lots when using a negative patient sample or a negative control.

FDAJun 11, 2004IN• Abbott Laboratories HPD/ADD/GPRD

Abbott Laboratories, Inc: ARCHITECT c8000 Processing Module; List Number 01G06-01. ...

Process change in the manufacturing of the AC/DC driver board used on the analyzer may result in one or more of the solid state relays to fail during use.

FDAJun 10, 2004Nationwide• Abbott Laboratories, Inc

Fobus GLT Gun Holsters (First Samco) – Design Malfunction (2004)

The gun holsters are designed to hold a Series 17 and Series 19 Glock handgun fitted with a laser-sight light. "GL 2*EMZ" is engraved in the top of the gun holster and "FOBUS" and "MADE IN ISRAEL" is printed on the back of the gun holster. This recall involves two early versions of the Fobus GLT gun holsters, one with a plastic retention strap less than one inch wide and one with a leather retention strap less than one inch wide. The new design includes a strap that is more than one inch wide, with a plastic tip too wide to be caught inside the trigger guard.

CPSCJun 9, 2004Nationwide• First Samco, Inc., through its Fobus USA Holster Division, of Southampton, Pa.

Kiddie Car Cruisers (Far East Brokers) – Ride-On Toy Safety Issue (2004)

The Kiddie Car Cruiser is a battery-operated ride-on toy car that measures about 27 inches high by 30 inches wide and 44 inches long. "Turbo" and "Cruiser" are printed on labels on the side of the ride-on toys.

CPSCJun 9, 2004Nationwide• Far East Brokers and Consultants Inc. (FEBC), of Jacksonville, Fla.

Dade Behring Inc. Rte 896, Glasgow Business Community: Berichrom Heparin Reagent (OWLD11). The reagent is a co...

Customers have reported a high rate of instrument error flags and calibration issues when using affected reagent.

FDAJun 7, 2004AZ, CA, CO +20 more• Dade Behring Inc. Rte 896, Glasgow Business Community

Bio-Rad Laboratories Inc: Bio-Rad brand ''TOX/See Drug Screen Test''; Catalog numb...

The device was producing false negative results for cocaine tests.

FDAJun 4, 2004IN• Bio-Rad Laboratories Inc

Abbott Health Products, Inc.: TDx/TDxFLx Opiates Reagent, Product list number: 9673-60

Abbott Diagnostics Division has found that the oxymorphone cross-reactivity information in the 'Specific Performance Characteristics' section of the TDx/TDxFLx Opiates Reagent package insert (commodity number 32-2087/R5) does not match the current product performance.

FDAMay 28, 2004Nationwide• Abbott Health Products, Inc.

Backyard Products Swings (Backyard Products™, of Collingwood, Ontario, Canada) – fall hazard (2004)

This recall involves single swings and acrobatic swings sold separately or as part of the Backyard Products wood gym set. Additional options to the gym sets include overhead ladders, slides, swings, and forts. A yellow, triangular metal gusset on the gym sets contains the brand name, "Backyard Products™" followed by "Collingwood, ON Canada." Model names and numbers are located on the assembly instructions.

CPSCMay 27, 2004Nationwide• Backyard Products™, of Collingwood, Ontario, Canada

Boston Scientific Corporation: PASV Central Venous Catheter, 7F, Cat. # CVC702IK, Model...

Kits labeled to contain 0.028" guidewire contain 0.038" guidewire.

FDAMay 25, 2004IN• Boston Scientific Corporation