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All Product Recalls

78,569 recalls

Source:AllCPSCFDAUSDASeverity:AllCriticalHighMedium
High RiskFDA
Philips Medical Systems Nederlands
Achieva 3.0T X-series, Model Number 781277. Nuclear Magnetic Resonance Imaging System
Medical Devices·11,226 affected·Dec 21, 2018
High RiskFDA
Philips Medical Systems Nederlands
Ingenia 1.5T, Model Number 781396. Nuclear Magnetic Resonance Imaging System
Medical Devices·11,226 affected·Dec 21, 2018
High RiskFDA
Philips Medical Systems Nederlands
Achieva 7.0T, Model Number 781240. Nuclear Magnetic Resonance Imaging System
Medical Devices·11,226 affected·Dec 21, 2018
High RiskFDA
Philips Medical Systems Nederlands
Intera 1.5T Omni/Stellar, Model Number 781104. Nuclear Magnetic Resonance Imaging System
Medical Devices·11,226 affected·Dec 21, 2018
High RiskFDA
Philips Medical Systems Nederlands
Ingenia 1.5T S, Model Number 781347. Nuclear Magnetic Resonance Imaging System
Medical Devices·11,226 affected·Dec 21, 2018
High RiskFDA
Philips Medical Systems Nederlands
MARLIN 1.5T, Model Number 781474. Nuclear Magnetic Resonance Imaging System
Medical Devices·11,226 affected·Dec 21, 2018
High RiskFDA
Philips Medical Systems Nederlands
MR-OR 3.0T, Model Number 781438. Nuclear Magnetic Resonance Imaging System
Medical Devices·11,226 affected·Dec 21, 2018
High RiskFDA
Philips Medical Systems Nederlands
NZM101 Ingenia 1.5T Linac, Model Number 781483. Nuclear Magnetic Resonance Imaging System
Medical Devices·11,226 affected·Dec 21, 2018
High RiskFDA
Philips Medical Systems Nederlands
Achieva 3.0T X, Model Number 781344. Nuclear Magnetic Resonance Imaging System
Medical Devices·11,226 affected·Dec 21, 2018
High RiskFDA
Philips Medical Systems Nederlands
Intera 1.5T Power/Pulsar, Model Number 781105. Nuclear Magnetic Resonance Imaging System
Medical Devices·11,226 affected·Dec 21, 2018
High RiskFDA
Philips Medical Systems Nederlands
Intera 1.5T CV, Model Number 781107. Nuclear Magnetic Resonance Imaging System
Medical Devices·11,226 affected·Dec 21, 2018
CriticalFDA
Draeger Medical, Inc.
VentStar Basic (P) 180, Catalog Number MP00351 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduct...
Respiratory Devices·525 affected·Dec 21, 2018
High RiskFDA
Philips Medical Systems Nederlands
Ingenia 3.0T CX, Model Number 781271. Nuclear Magnetic Resonance Imaging System
Medical Devices·11,226 affected·Dec 21, 2018
CriticalFDA
Draeger Medical, Inc.
ID Circuit Basic 250, Catalog Number MP01348 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conductio...
Respiratory Devices·20 affected·Dec 21, 2018
High RiskFDA
Philips Medical Systems Nederlands
Ingenia 1.5T CX, Model Number 781261. Nuclear Magnetic Resonance Imaging System
Medical Devices·11,226 affected·Dec 21, 2018
High RiskFDA
Philips Medical Systems Nederlands
Multiva 1.5T, Model Number 781076. Nuclear Magnetic Resonance Imaging System
Medical Devices·11,226 affected·Dec 21, 2018
High RiskFDA
Philips Medical Systems Nederlands
Multiva 1.5T 16 R5, Model Number 781078. Nuclear Magnetic Resonance Imaging System
Medical Devices·11,226 affected·Dec 21, 2018
High RiskFDA
Philips Medical Systems Nederlands
Intera 1.0T Omni/Stellar, Model Number 781102. Nuclear Magnetic Resonance Imaging System
Medical Devices·11,226 affected·Dec 21, 2018
CriticalFDA
Edwards Lifesciences, Llc
Edwards Lifesciences Swan Ganz Thermodilution Catheter, REF 131VF7P Product Usage: The Swan-Ganz Thermodilution Catheter provides a d...
Cardiac Devices·9 affected·Dec 21, 2018
High RiskFDA
Philips Healthcare
DigitalDiagnost C50, Stationary X-ray System
Diagnostic Devices·2 affected·Dec 21, 2018
RecallUSDA
Jennie-o Turkey Store
Jennie-O Turkey Store Sales, Inc. Recalls Raw Ground Turkey Products due to Possible Salmonella Reading Contamination
Poultry·0 affected·Dec 21, 2018
RecallUSDA
Jennie-o Turkey Store
Jennie-O Turkey Store Sales, Inc. Retira Productos De Pavo Molido Crudo Debido A La Posible Contaminacin De Salmonella Reading
Pork·0 affected·Dec 21, 2018
CriticalCPSC
Northeast Hearth & Home, Sutter Home & Hearth, Wallace's Stove & Fireplace Hearth Stores And Other Stores Nationwide And Online From June 2014 Through March 2018 For About $5,500.
Miles Industries Recalls Gas Fireplaces Due to Burn Hazard
Consumer Products·1,000 affected·Dec 20, 2018
RecallCPSC
Wholesale Distributors To Installers Nationwide From August 2018 Through October 2018 For About $1,400 To $1,700 For Water Heaters And $3,800 For Combination Boilers.
Navien Recalls Tankless Water Heaters and Boilers Due to Risk of Carbon Monoxide Poisoning
Consumer Products·3,400 affected·Dec 20, 2018
High RiskFDA
Apple Foods, Inc.
Diced Onions, packaged in vacuum sealed clear polybags, 5 pounds each, four packages per case. Product is sold under brand name Apple Fo...
Produce·162 affected·Dec 20, 2018
CriticalFDA
Funky Chunky Llc
Nutty Choco Pop, 10 oz. bag. Sold in the following configurations: Item #101, Gift Box (contains 1-10 oz. bag), Item #1728 Holiday Cro...
Food·2,214 affected·Dec 20, 2018
High RiskFDA
Apple Foods, Inc.
Diced Celery, packaged in vacuum sealed clear polybags, 5 pounds each, four packages per case. Product is sold under brand name Apple Fo...
Food·73 affected·Dec 20, 2018
High RiskFDA
Apple Foods, Inc.
Coleslaw (shredded white cabbage), packaged in vacuum sealed clear polybags, 5 pounds each, four packages per case. Product is sold unde...
Food·72 affected·Dec 20, 2018
High RiskFDA
Apple Foods, Inc.
Country Salad is a mixed product and it consists of Iceberg Lettuce, Romaine Lettuce, Shredded Carrots, Shredded Cabbage, and Sliced Radi...
Produce·488 affected·Dec 20, 2018
High RiskFDA
Apple Foods, Inc.
Diced Carrots, packaged in vacuum sealed clear polybags, 5 pounds each, four packages per case. Product is sold under brand name Apple F...
Food·79 affected·Dec 20, 2018
CriticalFDA
Lupin Pharmaceuticals Inc.
Ceftriaxone for Injection USP, 250 mg, packaged in a) one Single Use Vial (NDC 68180-611-01) and b) 10 Single Use Vials per box (NDC 6818...
Injectable Drugs·12,000 affected·Dec 20, 2018
CriticalFDA
Lupin Pharmaceuticals Inc.
Ceftriaxone for Injection USP, 500 mg, packaged in a) one Single Use Vial (NDC 68180-622-01) and b) 10 Single Use Vials per box (NDC 6818...
Injectable Drugs·8,000 affected·Dec 20, 2018
High RiskFDA
Torrent Pharma Inc.
LOSARTAN POTASSIUM TABLETS, USP, 25 mg, 90-count bottle (NDC: 13668-113-90), Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indra...
Oral Drugs·43,416 affected·Dec 20, 2018
CriticalFDA
Lupin Pharmaceuticals Inc.
Ceftriaxone for Injection USP, 1 g, packaged in a) one Single Use Vial (NDC 68180-633-01) and b) 10 Single Use Vials per box (NDC 68180-6...
Injectable Drugs·35,000 affected·Dec 20, 2018
RecallFDA
Akorn Inc
COSOPT Ophthalmic Solution, USP, (2% Dorzolamide Hydrochloride, 0.5% Timolol Maleate), 10 mL dropper bottle, Sterile, Rx only, Distribute...
Ophthalmic Drugs·30,794 affected·Dec 20, 2018
High RiskFDA
Torrent Pharma Inc.
LOSARTAN POTASSIUM TABLETS, USP, 100 mg, a) 30-count (NDC: 13668-115-30), b) 90-count (NDC: 13668-115-90), c) 1000-count (NDC: 13668-115-...
Oral Drugs·83,016 affected·Dec 20, 2018
CriticalFDA
Lupin Pharmaceuticals Inc.
Ceftriaxone for Injection USP, 2 g, packaged in 10 Single Use Vials (NDC 68180-644-01) per box, Rx only, Manufactured for: Lupin Pharmace...
Injectable Drugs·3,792 affected·Dec 20, 2018
High RiskFDA
Allergan, Plc.
OZURDEX (dexamethasone intravitreal implant) 0.7 mg), 1 single-use plastic applicator contained within carton, Rx only, Allergan Inc Irvi...
Drugs·133,716 affected·Dec 20, 2018
High RiskFDA
Torrent Pharma Inc.
LOSARTAN POTASSIUM and HYDROCHLOROTHIAZIDE TABLETS, USP, 100 mg/12.5 mg, a) 90-count bottle (NDC: 13668-117-90), b) 1000-count bottle (N...
Oral Drugs·18,852 affected·Dec 20, 2018
High RiskFDA
Torrent Pharma Inc.
LOSARTAN POTASSIUM and HYDROCHLOROTHIAZIDE TABLETS, USP 50 mg/12.5 mg, a) 90-count bottle (NDC: 13668-116-90), b) 1000-count bottle (NDC...
Oral Drugs·18,780 affected·Dec 20, 2018
RecallFDA
Amerigen Pharmaceuticals Inc.
Temozolomide Capsules, 180 mg, packaged in a 14 count bottles, Rx only, Mfd, by: Stason Pharmaceuticals, Inc., Irvine, CA, Dist. By: Amer...
Oral Drugs·771 affected·Dec 20, 2018
High RiskFDA
Torrent Pharma Inc.
LOSARTAN POTASSIUM TABLETS, USP, 50 mg, a) 30-count bottle (NDC: 13668-409-30), b) 90-count bottle (NDC: 13668-409-90), c) 1000-count bot...
Oral Drugs·65,832 affected·Dec 20, 2018
RecallFDA
Amerigen Pharmaceuticals Inc.
Temozolomide Capsules, 20 mg, packaged in a a) 5-count (NDC 43975-253-05) and b) 14 count (NDC 43975-253-14) bottles, Rx only, Mfd, by: S...
Oral Drugs·3,552 affected·Dec 20, 2018
High RiskFDA
Ge Healthcare, Llc
GE Healthcare Centricity Universal Viewer Breast Imaging Centricity Universal Viewer is a device that displays medical images and d...
Diagnostic Devices·297 affected·Dec 20, 2018
High RiskFDA
Steris Corporation
AMSCO 5000 Series Washer/Disinfector Model # 5052
Medical Devices·68 affected·Dec 20, 2018
High RiskFDA
Steris Corporation
AMSCO 3000 Series Washer/Disinfector Model # 3052
Medical Devices·11 affected·Dec 20, 2018
High RiskFDA
Abbott Gmbh & Co. Kg
Alinity i Processing Module, (a) Part Number 03R65-01 (b) Part Number A-30108552-01 (c) Part Number A-30109694-01 Product Usage:...
Diagnostic Devices·434 affected·Dec 20, 2018
CriticalFDA
Terrific Care Llc
CoaguChek XS PT Test; All Catalog/REF Numbers that do NOT end in 160 The CoaguChek XS PT test strips are part of the CoaguChek XS Syst...
Medical Devices·793 affected·Dec 20, 2018