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[Recalled] Digital Concepts Compact Travel Charger — The charger holds two AA or AAA batteries, is silver colored and has a sticker… | CPSC 2012-04-19

CPSC recall notice for Digital Concepts Compact Travel Charger. Reason: The charger holds two AA or AAA batteries, is silver colored and has a sticker…. Issued

[Recalled] Classic Series Circular Saw Blade 3-Pack — This recall involves Irwin Classic Series 10-inch Circular Saw Blade Limited Pr… | CPSC 2012-04-19

CPSC recall notice for Classic Series Circular Saw Blade 3-Pack (Irwin Industrial Tool Company, Huntersville, N.C.). Reason: This recall involves Irwin Classic

[Recalled] Medrad(R) Continuum MR Infusion System Standard Administration Kit Peristaltic Pump System designed for patients who require medications and other fluids during an MR procedure. It is intended to provide infusion therapy direc

FDA recall notice for Medrad(R) Continuum MR Infusion System Standard Administration Kit Peristaltic Pump System designed for patients who require medication

[Recalled] Medrad(R) Continuum MR Infusion System Primary Set Peristaltic Pump System designed for patients who require medications and other fluids during an MR procedure. It is intended to provide infusion therapy directly prior to, du

FDA recall notice for Medrad(R) Continuum MR Infusion System Primary Set Peristaltic Pump System designed for patients who require medications and other flui

[Recalled] Bacterin International, Inc., Osteoselect Demineralized Bone Matrix DMB Putty; Graft ID# B090056-664 Donor# B090056 2.5cc Expiration Date: 12/25/2011; LBL 210-0010-1 REV: 040109; and Graft ID# B090056-675. Bone void filler fo

FDA recall notice for Bacterin International, Inc., Osteoselect Demineralized Bone Matrix DMB Putty; Graft ID# B090056-664 Donor# B090056 2.5cc Expiration Date

[Recalled] Medrad(R) Continuum MR Infusion System Primary Spike Set Peristaltic Pump System designed for patients who require medications and other fluids during an MR procedure. It is intended to provide infusion therapy directly prior

FDA recall notice for Medrad(R) Continuum MR Infusion System Primary Spike Set Peristaltic Pump System designed for patients who require medications and othe

[Recalled] Medrad(R) Continuum MR Infusion System Primary VSA Set Peristaltic Pump System designed for patients who require medications and other fluids during an MR procedure. It is intended to provide infusion therapy directly prior to

FDA recall notice for Medrad(R) Continuum MR Infusion System Primary VSA Set Peristaltic Pump System designed for patients who require medications and other

[Recalled] Medrad(R) Continuum MR Infusion System Secondary VSA Set Peristaltic Pump System designed for patients who require medications and other fluids during an MR procedure. It is intended to provide infusion therapy directly prior

FDA recall notice for Medrad(R) Continuum MR Infusion System Secondary VSA Set Peristaltic Pump System designed for patients who require medications and othe

[Recalled] Medrad(R) Continuum MR Infusion System Side Step Set Peristaltic Pump System designed for patients who require medications and other fluids during an MR procedure. It is intended to provide infusion therapy directly prior to,

FDA recall notice for Medrad(R) Continuum MR Infusion System Side Step Set Peristaltic Pump System designed for patients who require medications and other fl

[Recalled] Medrad(R) Continuum MR Infusion System Secondary Spike Set Peristaltic Pump System designed for patients who require medications and other fluids during an MR procedure. It is intended to provide infusion therapy directly prio

FDA recall notice for Medrad(R) Continuum MR Infusion System Secondary Spike Set Peristaltic Pump System designed for patients who require medications and ot

[Recalled] Medrad(R) Continuum MR Infusion System Secondary Administration Kit Peristaltic Pump System designed for patients who require medications and other fluids during an MR procedure. It is intended to provide infusion therapy dire

FDA recall notice for Medrad(R) Continuum MR Infusion System Secondary Administration Kit Peristaltic Pump System designed for patients who require medicatio

[Recalled] Dried Brewers Yeast TG_YFS004 Naturex 375 Huyler Street, South Hackensack, NJ 07606 USA Phone: 1 201 440 5000 Net Wt 25 kg — The affected lots were tested and found to contain an unusual high level of sel… | FDA 2012-04-18

FDA recall notice for Dried Brewers Yeast TG_YFS004 Naturex 375 Huyler Street, South Hackensack, NJ 07606 USA Phone: 1 201 440 5000 Net Wt 25 kg (Naturex Inc.)

[Recalled] Gas Grills — This recall involves STOK Island and STOK Quattro gas grills | CPSC 2012-04-18

CPSC recall notice for Gas Grills. Reason: This recall involves STOK Island and STOK Quattro gas grills. Issued 2012-04-18.

[Recalled] Bicycle Brake Levers — The recalled products are Tektro TL-83 brake levers | CPSC 2012-04-18

CPSC recall notice for Bicycle Brake Levers. Reason: The recalled products are Tektro TL-83 brake levers. Issued 2012-04-18.

[Recalled] Evanix Speed and Conquest Air Rifles — This recall involves Evanix Speed .177, .22 and .25 caliber rifles and Evanix C… | CPSC 2012-04-18

CPSC recall notice for Evanix Speed and Conquest Air Rifles (Meca Evanix of South Korea). Reason: This recall involves Evanix Speed .177, .22 and .25 caliber ri

[Recalled] 94" (239cm) 20 Drop Admin Set w/High Pressure 4-Way (300 psi) Stopcock, Rotating Luer, Non-DEHP Tubing — The firm initiated the recall due to a molding defect in a high pressure stopco… | FDA 2012-04-17

FDA recall notice for 94" (239cm) 20 Drop Admin Set w/High Pressure 4-Way (300 psi) Stopcock, Rotating Luer, Non-DEHP Tubing (ICU Medical, Inc.). Reason: The f

[Recalled] Flush Kit w 3 Way Off Stopcock Product Usage: Flush Kit — The firm initiated the recall due to a molding defect in a high pressure stopco… | FDA 2012-04-17

FDA recall notice for Flush Kit w 3 Way Off Stopcock Product Usage: Flush Kit (ICU Medical, Inc.). Reason: The firm initiated the recall due to a molding de

[Recalled] Crispy by TWI Foods Pistachio Cookies, Biscuit, Net Wt 400 g, Product of Canada Manufactured by TWI Foods Inc. 2600 Drew Road, Mississauga, Ont, Canada L4T3M5. — Product may contain undeclared milk and almond | FDA 2012-04-17

FDA recall notice for Crispy by TWI Foods Pistachio Cookies, Biscuit, Net Wt 400 g, Product of Canada Manufactured by TWI Foods Inc. 2600 Drew Road, Mississauga

[Recalled] Bulk Foods, Inc. Yellow Corn Meal, Regular Roast, 25 lb; Bulk Foods, Inc. Yellow Corn Meal, Regular Roast, 50 lb — FDA samples of product tested positive for Fumonisin | FDA 2012-04-17

FDA recall notice for Bulk Foods, Inc. Yellow Corn Meal, Regular Roast, 25 lb; Bulk Foods, Inc. Yellow Corn Meal, Regular Roast, 50 lb (Haldeman Mills). Reason:

[Recalled] Pediatric electrolyte, Fruit Punch flavor---oral electrolyte solution---helps replace fluids & electrolytes---8 FL OZ (236 mL)---UPC Code: 31191129235 Distributed by Duane Reade/(866)375-6925---440 Ninth Ave., NY, NY 10001---Ite

FDA recall notice for Pediatric electrolyte, Fruit Punch flavor---oral electrolyte solution---helps replace fluids & electrolytes---8 FL OZ (236 mL)---UPC Code: