🔍 ProductGuru

Articles about: United States

55715 articles — Page 149 of 2786

[Recalled] Kroger Fresh Selections Greener Supreme; Iceberg lettuce, Romaine lettuce, Carrots and Red Cabbage; 12 oz plastic bag. Best if used by date: June 19, 2012: UPC 0 11110 91039 4 Distributed by the Kroger Co., Cincinnati, OH

FDA recall notice for Kroger Fresh Selections Greener Supreme; Iceberg lettuce, Romaine lettuce, Carrots and Red Cabbage; 12 oz plastic bag. Best if used by

[Recalled] Philips HeartStart MRx monitor/defibrillators Models: M3535A, M3536A, M3536M4, M3536M5, and M3536M6 Product Usage: The Heartstart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. Th

FDA recall notice for Philips HeartStart MRx monitor/defibrillators Models: M3535A, M3536A, M3536M4, M3536M5, and M3536M6 Product Usage: The Heartstart MRx

[Recalled] Siemens syngo.plaza Radiological Image Processing System Usage: Radiological Image Processing System — Firm has become aware of an unintended behavior when using syngo.plaza and issu… | FDA 2012-06-20

FDA recall notice for Siemens syngo.plaza Radiological Image Processing System Usage: Radiological Image Processing System (Siemens Medical Solutions USA, In

[Recalled] Select Medical Products Vinyl Powder-Free Exam Gloves, Medium Model # 6370 and Large Model # 6371, 100 per box; 10 boxes per case. Usage: Patient Examination. — Gulf South Medical Supply recalled their Select Medium and Large

FDA recall notice for Select Medical Products Vinyl Powder-Free Exam Gloves, Medium Model # 6370 and Large Model # 6371, 100 per box; 10 boxes per case. Usag

[Recalled] Philips HeartStart MRx monitor/defibrillators Models: M3535A and M3536A, M3536J, M3536M, M3536MC, M3536M1, M3536M2, M3536M3, M3536M4, M3536M5, M3536M6 The Heartstart MRx is for use for the termination of ventricular tachycard

FDA recall notice for Philips HeartStart MRx monitor/defibrillators Models: M3535A and M3536A, M3536J, M3536M, M3536MC, M3536M1, M3536M2, M3536M3, M3536M4, M35

[Recalled] Philips HeartStart MRx M3536A Defibrillator/Monitor with Software R.03.03 The Heartstart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical pe

FDA recall notice for Philips HeartStart MRx M3536A Defibrillator/Monitor with Software R.03.03 The Heartstart MRx is for use for the termination of ventricu

[Recalled] System 8000 Base Product Usage: The Sarns Modular Perfusion System 8000 is indicated for use for up to 6 hours on the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass

FDA recall notice for System 8000 Base Product Usage: The Sarns Modular Perfusion System 8000 is indicated for use for up to 6 hours on the extracorporeal

[Recalled] Frigidaire Self-Clean Gas Range — This recall for inspection and/or repair involves Frigidaire Gas Ranges Model #… | CPSC 2012-06-20

CPSC recall notice for Frigidaire Self-Clean Gas Range (Frigidaire, of Charlotte, N.C.). Reason: This recall for inspection and/or repair involves Frigidaire Ga

[Recalled] Portable Space Heater and Portable Oscillating Space Heater — This recall is of two models of 1500 watt Climate Keeper ceramic heaters | CPSC 2012-06-20

CPSC recall notice for Portable Space Heater and Portable Oscillating Space Heater. Reason: This recall is of two models of 1500 watt Climate Keeper ceramic hea

[Recalled] Product is labeled in part: "***LEASA Living Alfalfa Sprouts***CHOLESTEROL FREE***PRESERVATIVE FREE***KEEP REFRIGERATED***NET WT. 6 OZ. (168 g)***" Product is packaged in 6 oz clear plastic containers with UPC 75465-5591

FDA recall notice for Product is labeled in part: "***LEASA Living Alfalfa Sprouts***CHOLESTEROL FREE***PRESERVATIVE FREE***KEEP REFRIGERATED***NET WT. 6 OZ. (

[Recalled] Stryker brand Arthroscope and Hardware Set Tray (sterilization tray); Model/Part Number: 233-032-116; Product is manufactured and distributed by Stryker Endoscopy, San Jose, CA The Arthroscope and Hardware Set Tray is used t

FDA recall notice for Stryker brand Arthroscope and Hardware Set Tray (sterilization tray); Model/Part Number: 233-032-116; Product is manufactured and distribu

[Recalled] STERRAD 100S Cassette, Batch # 12A077. The STERRAD 100S and STERRAD NX sterilizations systems are low-temperature general purpose sterilizers used to sterilize heat and moisture sensitive reusable medical devices. The sterilan

FDA recall notice for STERRAD 100S Cassette, Batch # 12A077. The STERRAD 100S and STERRAD NX sterilizations systems are low-temperature general purpose steri

[Recalled] EOS X-ray Medical Diagnostic , X-ray Equipment System Digital Radiography used in general radiographic examination. — It was discovered of several generator failures of the EOS System due to failur… | FDA 2012-06-19

FDA recall notice for EOS X-ray Medical Diagnostic , X-ray Equipment System Digital Radiography used in general radiographic examination. (Eos Imaging Inc).

[Recalled] STERRAD NX Cassette, Batch # 12A078. The STERRAD 100S and STERRAD NX sterilizations systems are low-temperature general purpose sterilizers used to sterilize heat and moisture sensitive reusable medical devices. The sterilant

FDA recall notice for STERRAD NX Cassette, Batch # 12A078. The STERRAD 100S and STERRAD NX sterilizations systems are low-temperature general purpose sterili

[Recalled] Sterile Access & Return Line Set, 36" Length, Part # UM-872-36. Intended for use with medically prescribed hemodialysis blood tubing. — The recalled product leaks at the connection site | FDA 2012-06-19

FDA recall notice for Sterile Access & Return Line Set, 36" Length, Part # UM-872-36. Intended for use with medically prescribed hemodialysis blood tubing.

[Recalled] CareFusion EnVe Ventilator Designed for use on patients who require respiratory support or mechanical ventilation and weigh a minimum of 5 kg (11 lbs). It is suitable for service in hospital and transport environments as a sou

FDA recall notice for CareFusion EnVe Ventilator Designed for use on patients who require respiratory support or mechanical ventilation and weigh a minimum o

[Recalled] Thomas Lighting ceiling flush mount light fixtures — This recall involves 28 different models of ceiling flush-mounted light fixture… | CPSC 2012-06-19

CPSC recall notice for Thomas Lighting ceiling flush mount light fixtures (Thomas Lighting, of Elgin, Ill; part of Philips Consumer Luminaires Corporation). Rea

[Recalled] Outdoor wall mount lanterns — This recall involves outdoor wall-mount lanterns made of cast aluminum in a rus… | CPSC 2012-06-19

CPSC recall notice for Outdoor wall mount lanterns (Zhongshan De Gao Lighting Co. Ltd.). Reason: This recall involves outdoor wall-mount lanterns made of cast a

[Recalled] Air movers/blowers — This recall involves air movers/blowers that are used to dry floors in homes an… | CPSC 2012-06-19

CPSC recall notice for Air movers/blowers (EDIC, of Los Angeles, Calif.). Reason: This recall involves air movers/blowers that are used to dry floors in homes a

[Recalled] Giusto's Wheat Germ, Raw, Net Wt. 25 lb, (11.34 Kg) paper bag; Item number: 154205 Giusto's 344 Littlefield Ave. South Francisco, CA 94080 — Firm was notified by supplier that Wheat germ product is contaminated with meta… |

FDA recall notice for Giusto's Wheat Germ, Raw, Net Wt. 25 lb, (11.34 Kg) paper bag; Item number: 154205 Giusto's 344 Littlefield Ave. South Francisco, CA