-
Indomethacin Extended-Release Capsules USP, 75 mg, 100-count bottle… recall
FDA
· KVK Tech, Inc. · Class II
-
Airsupra (albuterol and budesonide) inhalation aerosol… recall
FDA
· AsttraZeneca Pharmaceuticals LP · Class II
-
Esomeprazole Magnesium for Delayed-Release Oral Suspension, 20 mg… recall
FDA
· Zydus Pharmaceuticals (USA) Inc · Class II
-
Esomeprazole Magnesium for Delayed-Release Oral Suspension, 40 mg… recall
FDA
· Zydus Pharmaceuticals (USA) Inc · Class II
-
BD ChloraPrep Clear, 2% x/v chlorhexidine gluconate (CHG) and 70% v/v… recall
FDA
· CareFusion 213, LLC · Class II
-
Macy's Recalls Holiday Lane Infant Footed Pajamas Due to Injury Hazard; Sold Exclusively by Macy's
CPSC
· Macy's
-
SmartPath to dStream for 3.0T, Model Number: 782145 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
SmartPath to dStream for 1.5T, Model Number: 782146 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Intera CV, Model Number: 781107 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Intera 3.0T Quasar Dual, Model Number: 781150 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Intera 1.5T R11, Model Number: 781170 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Intera 1.5T Power/Pulsar, Model Number: 781105 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Intera 1.5T Omni/Stellar, Model Number: 781104 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Intera 1.5T Master/Nova, Model Number: 781106 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Intera 1.5T Explorer/Nova Dual, Model Number: 781108 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Intera 1.5T, Model Numbers: 781195 and 781295 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Intera 1.0T Power/Pulsar, Model Number: 781103 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Intera 1.0T Omni/Stellar, Model Number: 781102 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Intera 0.5T Standard, Model Number: 781101 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Enterprise 1.5T, Model Number: 781145 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
KliniTray Platte Faxitron ,groB "R" sterile recall
FDA
· Klinika Mdical Gmb · Class II
-
KliniTray recall
FDA
· Klinika Mdical Gmb · Class II
-
Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395 recall
FDA
· Medline Industries, LP · Class II
-
Centurion Sterile Weitlaner Retractor, Reorder: 67315 recall
FDA
· Medline Industries, LP · Class II
-
CMS8000 Patient Monitor recall
FDA
· Contec Medical Systems Co., Ltd. · Class II
-
LifeShield Drug Library Management (DLM), LifeShield Infusion Safety… recall
FDA
· ICU Medical, Inc. · Class II
-
Augmedics Perc Pin Adaptor, Model recall
FDA
· Augmedics Ltd. · Class II
-
Pruitt Irrigation Occlusion Catheter recall
FDA
· LeMaitre Vascular, Inc. · Class II
-
Pruitt Occlusion Catheter recall
FDA
· LeMaitre Vascular, Inc. · Class II
-
TufTex Over-the-Wire Embolectomy Catheter recall
FDA
· LeMaitre Vascular, Inc. · Class II
-
Alinity m Resp-4-Plex AMP Kit, List Number 09N79-096… recall
FDA
· Abbott Molecular, Inc. · Class II
-
Alinity m Resp-4-Plex Amplification (AMP) Kit (CE), List Number 09N79-090… recall
FDA
· Abbott Molecular, Inc. · Class II
-
FoundationOne Companion Diagnostic (F1CDx) recall
FDA
· Foundation Medicine, Inc. · Class II
-
Contour Product Name: Contour Gold Eyelid Weight Model recall
FDA
· Meddev Corp · Class II
-
Contour Product Name: Contour Gold Eyelid Weight Model recall
FDA
· Meddev Corp · Class II
-
Halyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit recall
FDA
· AVID Medical, Inc. · Class II
-
Halyard SUTURE PACK CABG. Cardiovascular Procedure Convenience Kit recall
FDA
· AVID Medical, Inc. · Class II
-
Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit recall
FDA
· AVID Medical, Inc. · Class II
-
MedicaLyte Liquid Bicarbonate Concentrate recall
FDA
· Nipro Renal Soultions USA, Corporation · Class I
-
iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Oxygen Concentrator… recall
FDA
· Medical Depot Inc. · Class I
-
AirLife Product Name: AirLife Infant Heated Wire Circuit Model recall
FDA
· Vyaire Medical · Class I
-
AirLife Product Name: AirLife Infant Heated Wire Circuit Model recall
FDA
· Vyaire Medical · Class I
-
Testosterone Cypionate Injection, 200 mg/mL, CIII, Rx Only… recall
FDA
· Empower Pharmacy · Class II
-
La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne… recall
FDA
· L'Oreal USA · Class II
-
La Roche-Posay Laboratoire Dermatologique Effaclar Dermatological Acne… recall
FDA
· L'Oreal USA · Class II
-
La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne… recall
FDA
· L'Oreal USA · Class II
-
BuddyLove Recalls Children's Mini Danica Loungewear Sets Due to Risk of Serious Injuries or Death from Burn Hazard…
CPSC
· BuddyLove
-
Polaris Industries Recalls Ranger XP 1000 NorthStar and Ranger XP 1000 NorthStar Crew Recreational Off-Road Vehicles Due to Injury Hazard
CPSC
· Polaris Industries
-
KTM Recalls Off-Road Motorcycles Due to Crash Hazard Recall
CPSC
· KTM North America, Inc.
-
Fat Brain Recalls Rollers Tile Toys Used in PlayTab Modular Activity Boards Due to Magnet Ingestion Hazard…
CPSC
· Fat Brain
-
IntelliSpace Cardiovascular software versions 6.x, 7.x, and 8.x recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Blueprint Software, BPUE001. Intended for use by surgeons as a pre… recall
FDA
· Tornier S.A.S. · Class II
-
Introducer Kit- Tearaway MicroSlide recall
FDA
· Galt Medical Corporation · Class II
-
Introducer Needle recall
FDA
· Galt Medical Corporation · Class II
-
Introducer Kit- Coaxial Dilator recall
FDA
· Galt Medical Corporation · Class II
-
GALT Guidewire recall
FDA
· Galt Medical Corporation · Class II
-
B Braun Interventional ELITE HV Hemostasis Valve Introducer System recall
FDA
· Galt Medical Corporation · Class II
-
B Braun Interventional Coaxial Dilator recall
FDA
· Galt Medical Corporation · Class II
-
GALT Centeze Catheter recall
FDA
· Galt Medical Corporation · Class II
-
Philips Tempus Pro Patient Monitor recall
FDA
· Remote Diagnostic Technologies Ltd. · Class II