55716 articles — Page 179 of 2786
FDA recall notice for NIDEK Medical M5C5/ MARK5 NUVO/STD, 230 V~50/60 Hz - 420 W. Oxygen Concentrator. (Nidek Medical Products Inc). Reason: Capacitor failur
CPSC recall notice for Farm Glass & Metal Spiral Tea Light Holder. Reason: This recall involves a decorative spiral tea light holder made from a painted g…. Iss
FDA recall notice for Organic 100% Pomegranate Juice packed in glass bottles Smart Juice Organic Pomegranate 100% Juice 33.8 FL. Oz. 100% Juice Distributed
FDA recall notice for Nextgen Complete Knee Solution Replacement Jaw for Use with Femoral and Provisional Impactor/Extractor, REF 00-5901-026-40, Non-Sterile Zi
FDA recall notice for ABG II Modular Hip Stem Stryker Howmedica Osteonics Corp. Mahwah, NJ 07430 Stryker Ireland Carrigtwohill Industrial Estate, Carrigtwohil
FDA recall notice for Nextgen Complete Knee Solution Femoral and Provisional Impactor/ Extractor, REF 00-5901-026-00, Non-Sterile Zimmer, Warsaw Indiana The
FDA recall notice for Siemens Mobilett Mira mobile x-ray system Product Usage: Mobile x-ray system (Siemens Medical Solutions USA, Inc). Reason: During re
FDA recall notice for Siemens Uroskop Access. Fluoroscopic, image intensified x-ray system (Siemens Medical Solutions USA, Inc). Reason: Siemens has discover
FDA recall notice for SunFresh Natural Fruit & Nut, Distributed by: Sunfresh Natural, LLC. Passaic, NJ 07055. Please visit us at: www.sunfreshnatural.com. 6 o
FDA recall notice for Newport Portable Package, Model #50000, Serial # 13591, 13592, 13604, 13606, 13614, 13662, 13663, 13664, 13726, 13731, 13733, 13736, 137
FDA recall notice for CM Flowmeter Pkg H, Model #36700, Serial # 13749 Product Usage: Conscious Sedation Unit Analgesia Gas Machine. (Accutron Inc). Rea
FDA recall notice for Flow Meter, CM Assembly, Model #27025, Serial # 13686, 13690, 13712, 13793. Flowmeter, CM Assembly, Model#31970, Serial#13692. Produ
FDA recall notice for Respironics Trilogy 100, 200, and 202 Ventilators The Respironics Trilogy systems provides continuous or intermittent ventilatory suppo
FDA recall notice for Patient Side Cart Battery Box used in conjunction with the da Vinci A surgical system. Intuitive Surgical Inc. Sunnyvale, CA 94086 (In
FDA recall notice for Lipofilter 3000, model ASP-CAN-2, labeled in part ***MicroAire, 1641 Edlich Drive, Charlottesville, VA 22911, USA*** Product Usage:
FDA recall notice for Stahl's Famous Original Bakery CUTOUT COOKIES 14oz. INGREDIENTS: Pastry Flour, Sugar, Shortening...Contains Wheat, Eggs, Milk and Soy. (JD
CPSC recall notice for Target Home Bunny Sippy Cup. Reason: The recall involves two styles of Target Home Bunny Sippy Cups. Issued 2012-04-26.
CPSC recall notice for Whoozit® Starry Time Rattle. Reason: This recall involves Whoozit® Starry Time baby rattles. Issued 2012-04-26.
CPSC recall notice for Teryx Recreational Off-Highway Vehicles. Reason: The recalled vehicles are model year 2012 Kawasaki four-wheel recreational off-…. Issued
CPSC recall notice for Gerber® Instant™ Knife. Reason: The recalled knives are spring-assisted clip knives with a black retractable 3.…. Issued 2012-04-26.