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Lifetime Brands Inc., of Westbury, N.Y.

Lifetime Brands Inc., of Westbury, N.Y. Recalls

All product recalls associated with Lifetime Brands Inc., of Westbury, N.Y..

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Recall Summary

Total Recalls

1000

Past Year

295

Class I (Serious)

116

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 4061–4080 of 4465 recalls

Fruit Slicer (Farberware) – Laceration Hazard (2006)

Laceration Risk

The recalled product is the Farberware® Classic Series™ Fruit Slicer and Corer with model number 78350. The model number is written on the packaging. The fruit slicer/corer is an eight-section round metal blade encircled in hard black plastic with two handles. "FARBERWARE" is printed on the top of the handle.

CPSCDec 19, 2006Nationwide• Lifetime Brands Inc., of Westbury, N.Y.

Abbott Diabetes Care, Inc.: Abbott Precision Link Software (Version 2.1), (Version 2....

If the time and date are not set correctly on both the user's meter and computer, there is the potential for incorrect times and dates to be assigned to the results in the Precision Link Software.

FDADec 18, 2006PR• Abbott Diabetes Care, Inc.

Terang Nusa Sdn Bhd 1, Jalan 8, Pengkalan Chepa 2, Ind Zone Kota Bharu Malaysia: Sterile Neolon 2G Latex-Free Powder-Free Neoprene Surgica...

Some of the packages labeled as latex-free actually contain latex gloves.

1...202 203204205 206...224

Page 204 of 224Next

FDADec 18, 2006Nationwide• Terang Nusa Sdn Bhd 1, Jalan 8, Pengkalan Chepa 2, Ind Zone Kota Bharu Malaysia

Bausch & Lomb Inc: Bausch & Lomb Millennium 20 Ga. High Speed Posterior Vitr...

Laceration Risk

The cutter tip could break during a procedure

FDADec 14, 2006Nationwide• Bausch & Lomb Inc

Bausch & Lomb Inc: Bausch & Lomb Lightning High Speed Vitrectomy Cutter, Cat...

Laceration Risk

The cutter tip could break during a procedure

FDADec 14, 2006Nationwide• Bausch & Lomb Inc

Bell Rattles (BRIO) – Choking Risk (2006)

Choking Hazard

This recall involves wooden rattles with six-multi-colored slats used to connect the two, red round ends. A metal bell is contained within the slats. The rattles measure 2 1/2 inches in diameter by 2 1/2 inches in height. The name BRIO appears on one of the wooden sides.

CPSCDec 13, 2006Nationwide• BRIO AB, of Sweden

Abbott Laboratories, Inc: ARCHITECT i2000 Processing Module, for in vitro diagnosti...

The re-designed ARCHITECT Temperature Controller Board has been identified as being susceptible to electromagnetic interference (EMI) in the laboratory. This can cause a board reset condition, stopping temperature control function of the board. Situation does not stop analyzer operation and does not generate an error condition alerting operator when condition occurs.

FDADec 12, 2006PR• Abbott Laboratories, Inc

Abbott Laboratories, Inc: ARCHITECT i2000SR Processing Module, for in vitro diagnos...

FDADec 12, 2006PR• Abbott Laboratories, Inc

Abbott Point of Care Inc.: i-STAT PT/INR Cartridge prothrombin time test in vitro di...

Patients treated with the antibiotic CUBICIN can cause a concentration dependent false prolongation of prothrombin time (PT) and elevation of INR (International Normalized Ratio) when using the i-STAT PT/INR cartridges.

FDADec 12, 2006Nationwide• Abbott Point of Care Inc.

Abbott Vascular-Cardiac Therapies dba Guidant Corporation: ACS DUOSTAT Rotating Hemostatic Valve, 0.096 inch, for us...

Specific lots of the .096' and .115' Rotating Hemostatic Valves (RHV) and the Duostat .096' Rotating Hemostatic Valve (RHV) potentially have an incomplete seal in the packaging pouch

FDADec 5, 2006Nationwide• Abbott Vascular-Cardiac Therapies dba Guidant Corporation

Abbott Vascular-Cardiac Therapies dba Guidant Corporation: ACS Rotating Hemostatic Valve, 0.096 inch, for use with a...

Specific lots of the .096' and .115' Rotating Hemostatic Valves (RHV) and the Duostat .096' Rotating Hemostatic Valve (RHV) potentially have an incomplete seal in the packaging pouch

FDADec 5, 2006Nationwide• Abbott Vascular-Cardiac Therapies dba Guidant Corporation

Abbott Laboratories MPG: ARCHITECT LH Reagent, each kit contains bottles of Anti-B...

The lots of ARCHITECT LH Reagent List 6C25-22, have the potential to generate patient specimen results that are elevated. Correlation studies have demonstrated an upward shift in slope for patient results of approximately 13% on average when compared to other currently available reagent lots and an average bias from patient specimens of 13% to 17% has been observed.

FDANov 22, 2006PR• Abbott Laboratories MPG

Bio-Rad Laboratories Inc: Bio-Rad D-10 Dual Program Calibrator Diluent, a component...

The Diluent in the D-10 Dual Program Calibrator reorder packs is defective, and can cause early calibration failure or elevated control and sample recovery results.

FDANov 17, 2006Nationwide• Bio-Rad Laboratories Inc

Biosense Webster, Inc.: Biosense Webster PREFACE Guiding Sheath, Multipurpose Sho...

Biosense Webster, Inc. has received a number of complaints regarding the radiopaque tip separating or partially detaching from the PREFACE Sheath during use in the left atrium.

FDANov 17, 2006Nationwide• Biosense Webster, Inc.

Abbott Spine: TraXis Fixed Rasp in sizes: 7mm, 9mm, 11mm, 13mm and 15mm...

Tip of devices may dislodge while in use during surgery.

FDANov 7, 2006Nationwide• Abbott Spine

Abbott Spine: TraXis Fixed Trial in sizes: 7mm, 9mm, 11mm, 13mm and 15m...

Tip of devices may dislodge while in use during surgery.

FDANov 7, 2006Nationwide• Abbott Spine

Abbott Laboratories: Abbott - CELL-DYN 1800 System with CELL-DYN 22 Calibrator...

Incorrect Results: Hemoglobin results in donor samples assayed on the CELL-DYN 1800 System vary more than expected across the range of claimed operating temperatures of 18 degrees Celcius to 30 degrees Celcius.

FDAOct 27, 2006PR• Abbott Laboratories

Biogenex Laboratories: Super Sensitive Link-Label IHC Detection System/Mega Volu...

Mislabeling: The product's "contents section " labeling (outer box) is mislabeled incorrectly printed as '1 x 100 mL Alk Phos Label' which should read '1 x 100 mL HRP Label'. A second, smaller label, incorrectly reads "RTU MultiLink HPR/AEC" which should be labeled as "RTU MultiLink HPR". The reagent vials in the box are correctly labeled.

FDAOct 3, 2006VA• Biogenex Laboratories

Abbott Laboratories Inc.: Phenobarbital- Reagent-Clinical Chemistry--List number: 1...

Erratic elevated results and or the inability to calibrate due to imprecision.

FDASep 26, 2006Nationwide• Abbott Laboratories Inc.

Abbott Point Of Care Inc.: i-STAT G3+ Cartridge: PCO2 Abbott Point of Care, Princeto...

Certain lots of G3+ cartridges may be difficult to fill.

FDASep 25, 2006Nationwide• Abbott Point Of Care Inc.