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All Product Recalls

78,569 recalls

Source:AllCPSCFDAUSDASeverity:AllCriticalHighMedium
High RiskFDA
Sca Pharmaceuticals
Ephedrine sulfate 5 mg/mL in 0.9% Sodium Chloride 10 mL in Single Dose Syringe, Total Volume 10 mL, Rx only, SCA Pharmaceuticals, 8821 K...
Drugs·1,248 affected·Dec 7, 2017
High RiskFDA
Johnson & Johnson
Neutrogena Acne Proofing whipped foam cleanser, (Salicylic Acid 2%), aerosolized product in a can, NET WT. 5 OZ (141 g) , Distributed by ...
Drugs·67,260 affected·Dec 7, 2017
High RiskFDA
Johnson & Johnson
Neutrogena Elevated 4-Holiday Trays (contains Neutrogena Deep Clean Purifying Whipped Foam Cleanser) Case Code: 00070501302866
Drugs·0 affected·Dec 7, 2017
High RiskFDA
Boston Scientific Corporation
PROPONENT SR Pacemaker
Cardiac Devices·0 affected·Dec 7, 2017
High RiskFDA
Boston Scientific Corporation
ACCOLADE DR Pacemaker
Cardiac Devices·0 affected·Dec 7, 2017
High RiskFDA
Boston Scientific Corporation
ACCOLADE SR Pacemaker
Cardiac Devices·0 affected·Dec 7, 2017
High RiskFDA
Boston Scientific Corporation
VISIONIST CRT-P Pacemaker
Cardiac Devices·0 affected·Dec 7, 2017
High RiskFDA
Boston Scientific Corporation
ESSENTIO DR Pacemaker
Cardiac Devices·0 affected·Dec 7, 2017
High RiskFDA
Boston Scientific Corporation
ALTRUA 2 EL DR Pacemaker
Cardiac Devices·0 affected·Dec 7, 2017
High RiskFDA
Boston Scientific Corporation
ACCOLADE MRI EL DR Pacemaker
Cardiac Devices·0 affected·Dec 7, 2017
High RiskFDA
Boston Scientific Corporation
PROPONENT DR Pacemaker
Cardiac Devices·0 affected·Dec 7, 2017
High RiskFDA
Boston Scientific Corporation
VALITUDE CRT-P Pacemaker
Cardiac Devices·0 affected·Dec 7, 2017
High RiskFDA
Boston Scientific Corporation
PROPONENT EL DR Pacemaker
Cardiac Devices·0 affected·Dec 7, 2017
High RiskFDA
Boston Scientific Corporation
ACCOLADE MRI DR Pacemaker
Cardiac Devices·0 affected·Dec 7, 2017
High RiskFDA
Boston Scientific Corporation
ACCOLADE MRI SR Pacemaker
Cardiac Devices·0 affected·Dec 7, 2017
High RiskFDA
Helena Laboratories, Corp.
Cascade Abrazo aPTT Test Card, Model 5722, For Export Only. The firm name on the label is Helena Laboratories, Beaumont, TX.
Medical Devices·21 affected·Dec 7, 2017
High RiskFDA
Boston Scientific Corporation
ESSENTIO SR Pacemaker
Cardiac Devices·0 affected·Dec 7, 2017
High RiskFDA
Zimmer Biomet, Inc.
6.5mm x 125mm x 16mm Cannulated Screw, Item Number: 110009948 (UDI: (01)00887868111327 (17)270421 (10)120910) Product Usage: The 6.5/...
Medical Devices·6 affected·Dec 7, 2017
High RiskFDA
Boston Scientific Corporation
ALTRUA 2 SR Pacemaker
Cardiac Devices·0 affected·Dec 7, 2017
High RiskFDA
Intel-ge Care Innovations Llc
Health Harmony Mobile application software Product Usage: Care Innovations Health Harmony Mobile is intended as a communication tool...
Medical Devices·1,302 affected·Dec 6, 2017
RecallCPSC
Industrial, Construction, Welding Supply Distributors, Including Purvis Industries, Weldstar Co., Pennsylvania Tool Sales And Service, And Online At Ohiopowertool.com From April 2017 Through October 2017 For About $350.
Metabo Recalls Rat Tail Angle Grinders Due to Laceration Hazard
Tools·1,100 affected·Dec 5, 2017
CriticalCPSC
Fry's Electronics Stores Nationwide And Online At Frys.com And Amazon.com From June 2017 Through October 2017 For About $20.
Netgear Recalls Power Adapters for Outdoor Cameras Due to Fire Hazard
Outdoor & Garden·7,300 affected·Dec 5, 2017
CriticalFDA
Creative Contract Packaging Corporation, Llc
HERB-OX Beef Flavor Granulated Bouillon, 4 ounce jars
Meat & Poultry·4,412 affected·Dec 5, 2017
CriticalFDA
Aldi Inc
Choceur Dark Chocolate Bars, 5.29 oz., 20 units/case
Snacks & Candy·93,500 affected·Dec 5, 2017
RecallFDA
Sanofi-aventis U.s. Llc
Enoxaparin Sodium, Injection 120 mg/0.8 mL, pre-filled, packaged in 10-count cartons, Rx Only, Winthrop US., a business of Sanofi-aventis...
Injectable Drugs·11,474 affected·Dec 5, 2017
RecallCPSC
West Elm Stores Nationwide, West Elm's Catalog And Online At Www.westelm.com From June 2014 Through October 2017 For About $130 For The Lamp With A Usb And For Between $80 And $100 For The Lamp Without A Usb.
West Elm Recalls Table Lamps Due to Shock Hazard
Furniture·43,000 affected·Dec 4, 2017
RecallFDA
Mccain Foods Usa
Publix brand, item # 41596, Southern Style Diced Hash Brown Potatoes, Net wt. 32 oz. Retail's UPC # 0 41415 00549 5. The label is read...
Food·1,463 affected·Dec 4, 2017
High RiskFDA
Solco Healtcare Us Llc
Gabapentin Tablets, USP, 800 mg, 500-count, Rx only, Made in India, PONDRUGS/16 134193, Distributed by: Solco Healthcare US, LLC, Cranbur...
Oral Drugs·0 affected·Dec 4, 2017
CriticalFDA
Auromedics Pharma Llc
Pantoprazole Sodium for Injection, 40 mg per vial, single dose vial, Rx only, Manufactured in India for: AuroMedics Pharma LLC, 6 Wheelin...
Injectable Drugs·66,100 affected·Dec 4, 2017
High RiskFDA
Allergan
Viokace (pancrelipase) tablets, 20,880 USP units, 100-count bottle, Rx only, Distributed by; Allergan USA Inc., Irvine, CA 92612, Manufac...
Oral Drugs·12,699 affected·Dec 4, 2017
High RiskFDA
Smiths Medical Asd Inc.
PORT-A-CATH II PS/Titan, Tray PAC II. Labeled as: a. VEN LP, PU, 2.6MM, UL, 8.5FR/INTRO (1/EA); b. DL, LP, PU, 2.2MM, WING-LOCK...
Medical Devices·1,077 affected·Dec 4, 2017
High RiskFDA
Konica Minolta Medical Imaging Usa, Inc.
Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A8AR, UDI: 04560141941588
Medical Devices·17 affected·Dec 4, 2017
High RiskFDA
Beckman Coulter Inc.
iChem VELOCITY Urine Chemistry Strips, REF 800-7212 Product Usage: The iChem VELOCITY automated urine chemistry system is an in vitro...
Diabetes Devices·14,340 affected·Dec 4, 2017
High RiskFDA
Cellavision Ab
CellaVision DM Software versions 6.0.1 or 6.0.2 installed on the following products: CellaVision DM96, DM1200, DM9600 and DI-60 Produc...
Medical Devices·224 affected·Dec 4, 2017
High RiskFDA
Accord Media, Llc
Ultra Renew Plus
Medical Devices·1,040 affected·Dec 4, 2017
High RiskFDA
Konica Minolta Medical Imaging Usa, Inc.
Sonimage HS1 Ultrasound Kit AC adapter, Product Number: 1. A9RP, UDI: 04560141945463; 2. AAEU, UDI: 04560141946385; 3. A9RR, UDI: 0456014...
Medical Devices·30 affected·Dec 4, 2017
CriticalFDA
Physio-control, Inc.
LIFEPAK 20e DEFIBRILLATOR/MONITOR, 3201273 Product Usage: The LIFEPAK 20e defibrillator/monitor is intended for use in the hospital, ...
Cardiac Devices·3,831 affected·Dec 4, 2017
High RiskFDA
Life Technologies Corporation
Oncomine Dx Target Test User Guides and Assay Definition File, Model: A32461; UDI: (01)10190302006071(11)170911(10)1.8(240)A32461 The ...
Diagnostic Devices·9 affected·Dec 4, 2017
RecallCPSC
Powersports Dealers Nationwide From August 2016 Through May 2017 For About $4,800.
Camso Recalls Dirt to Snow Bike Conversion Kits Due to Crash and Impact Hazards
Bicycles & Wheeled Sports·280 affected·Dec 1, 2017
High RiskFDA
Elekta, Inc.
ELEKTA Digital Accelerator under the following brand names: Elekta Synergy, Synergy S, Synergy Platform, Precise Digital Accelerator, Inf...
Medical Devices·2,998 affected·Dec 1, 2017
High RiskFDA
Mako Surgical Corporation
RESTORIS MCK TIBIAL BASEPLATE-RM/LL used in unicompartmental knee arthroplasty and knee replacements.
Medical Devices·126 affected·Dec 1, 2017
High RiskFDA
Stryker Sustainability Solutions
3040-VenaFlow Calf Garment (Aircast) Quick Connect was mislabeled as 3010-PL Aircast Pos-Lock Connector. Intended for use in preventin...
Medical Devices·280 affected·Dec 1, 2017
High RiskFDA
Ohmeda Medical
Rotating IV Pole Rotating IV Pole falls under the category classified as capital equipment, an optional accessory that may be purcha...
Medical Devices·1,179 affected·Dec 1, 2017
RecallUSDA
Unknown
Rafedain Shish Kabob Restaurant, Inc. Recalls Chicken Patty Shish Kabob Products Due To Misbranding and Undeclared Allergens
Poultry·0 affected·Dec 1, 2017
RecallUSDA
Unknown
Rafedain Shish Kabob Restaurant, Inc. Retira Productos De Pincho (“Shish Kabob”) De Arne De Pollo Preparada Debido a un Error De Rotulación y Alérgenos No Declarados
Poultry·0 affected·Dec 1, 2017
RecallUSDA
Caesar's Pasta, Llc
Caesar's Pasta, LLC Recalls Beef Meatball Products Due To Misbranding and Undeclared Allergens
Beef·0 affected·Dec 1, 2017
RecallUSDA
Caesar's Pasta, Llc
Caesar’s Pasta, LLC Retira Productos De Albóndigas De Res Debido a un Error De Rotulación y Alérgenos No Declarados
Meat & Poultry·0 affected·Dec 1, 2017
RecallCPSC
Design Within Reach, Lumens, Ylighting, And Other Lighting Stores And Online At Flos.com From January 1996 Through December 2006 For Between $800 And $1,900.
Flos Recalls Pendant Light Fixtures Due to Impact Injury Hazard
Consumer Products·4,000 affected·Nov 30, 2017