Year

2019 Product Recalls

5,865 product recalls issued in 2019 across CPSC, FDA, and USDA datasets.

5,865 recalls
RecallFDA
Invagen Pharmaceuticals, Inc.
Testosterone Topical Solution 30mg of testosterone per pump actuation * each actuation delivers 1.5 mL of solution Total contents: 110 mL...
Topical Drugs·1,776 affected·Jun 12, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
AXIOM Artis dTC, Model Number 7413078
Medical Devices·98 affected·Jun 12, 2019
High RiskFDA
Becton Dickinson & Company
BD Vacutainer Lithium HeparinN (LH) 95 USP Units Blood Collection Tubes, Catalog Number 367886
Medical Devices·1,436,228,004 affected·Jun 12, 2019
High RiskFDA
Becton Dickinson & Company
BD Vacutainer PST Gel and Lithium HeparinN (LH) 56 Units Blood Collection Tubes, Catalog Number 367960
Medical Devices·1,436,228,004 affected·Jun 12, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
AXIOM Artis FA, Model Number 5904441
Medical Devices·4 affected·Jun 12, 2019
High RiskFDA
Becton Dickinson & Company
BD Vacutainer PST Gel and Lithium HeparinN (LH) 126 Units Blood Collection Tubes, Catalog Number 367964
Medical Devices·1,436,228,004 affected·Jun 12, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
Artis zee floor MN, Model Number 10094142
Medical Devices·23 affected·Jun 12, 2019
High RiskFDA
Becton Dickinson & Company
BD Vacutainer Lithium HeparinN (LH) 37 USP Units Blood Collection Tubes, Catalog Number 366664
Medical Devices·1,436,228,004 affected·Jun 12, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
AXIOM Artis dMP, Model Number 7555365
Medical Devices·32 affected·Jun 12, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
AXIOM Artis dBC, Model Number 7728392
Medical Devices·53 affected·Jun 12, 2019
High RiskFDA
Zoll Medical Corporation
ZOLL AED PRO Automated External Defibrillator Product Usage: The AED PRO unit is intended to defibrillate victims of ventricular fibr...
Cardiac Devices·1,969 affected·Jun 12, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
Artis zee ceiling, Model Number 10094137
Medical Devices·428 affected·Jun 12, 2019
High RiskFDA
Becton Dickinson & Company
BD Vacutainer LH (Lithium Heparin) 34 I.U. Plus Blood Collection Tubes, Catalog Number 368494
Medical Devices·1,436,228,004 affected·Jun 12, 2019
High RiskFDA
Becton Dickinson & Company
BD Vacutainer Lithium HeparinN (LH) 56 USP Units Blood Collection Tubes, Catalog Number 366667
Medical Devices·1,436,228,004 affected·Jun 12, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
AXIOM Artis dBA, Model Number 7555357
Medical Devices·85 affected·Jun 12, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
AXIOM Artis dFA, Model Number 7555373
Medical Devices·39 affected·Jun 12, 2019
High RiskFDA
Becton Dickinson & Company
BD Vacutainer PST Gel and Lithium HeparinN (LH) 56 Units Blood Collection Tubes, Catalog Number 368056
Medical Devices·1,436,228,004 affected·Jun 12, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
Artis zee floor, Model Number 10094135
Medical Devices·170 affected·Jun 12, 2019
High RiskFDA
Becton Dickinson & Company
BD Vacutainer PST Gel and Lithium HeparinN (LH) 83 Units Blood Collection Tubes, Catalog Number 367962
Medical Devices·1,436,228,004 affected·Jun 12, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
AXIOM Artis dTA, Model Number 7008605
Medical Devices·178 affected·Jun 12, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
Artis zee biplane, Model Number 10094141
Medical Devices·268 affected·Jun 12, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
Artis zeego, Model Number 10280959
Medical Devices·117 affected·Jun 12, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
Artis zee multi, Model Number 10094139
Medical Devices·89 affected·Jun 12, 2019
High RiskFDA
Becton Dickinson & Company
BD Vacutainer LH (Lithium Heparin) 68 I.U. Plus Blood Collection Tubes, Catalog Number 368884
Medical Devices·1,436,228,004 affected·Jun 12, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
AXIOM Artis TA, Model Number 7007755
Medical Devices·5 affected·Jun 12, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
AXIOM Artis dFC, Model Number 7727717
Medical Devices·19 affected·Jun 12, 2019
High RiskFDA
Beckman Coulter Inc.
SYNCHRON Systems Barbiturates Reagent (BARB 1 X 250); Catalog No. 475012 - Product Usage: BARB reagent, in conjunction with UniCel DxC 60...
Diagnostic Devices·10,145 affected·Jun 12, 2019
High RiskFDA
Becton Dickinson & Company
BD Vacutainer Lithium HeparinN 75 USP Units Blood Collection Tubes, Catalog Number 367884
Medical Devices·1,436,228,004 affected·Jun 12, 2019
RecallUSDA
Unknown
Pasture Raised Foods, LLC Recalls Raw Whole Poultry Products Produced Without Benefit of Inspection
Poultry·0 affected·Jun 12, 2019
RecallUSDA
Unknown
Pasture Raised Foods, LLC retira productos congelados de aves enteras producidos sin el beneficio de la inspección
Poultry·0 affected·Jun 12, 2019
CriticalCPSC
Online At Amazon.com, Amazon.ca, Amazon.com.mx From October 2017 Through March 2019 For Between $25 And $35.
Amazon Recalls AmazonBasics Ceramic Space Heaters Due to Fire and Burn Hazards (Recall Alert)
Heating & Cooling·377,000 affected·Jun 11, 2019
CriticalCPSC
Exclusively Online At Amazon.com From September 2018 Through March 2019 For About $109.
Cushy Form Recalls Folding Mattress Due to Violation of Federal Mattress Flammability Standard; Sold Exclusively at Amazon.com (Recall Alert)
Consumer Products·2,300 affected·Jun 11, 2019
RecallCPSC
Target Stores Nationwide, Online At Target.com, And On Google Express From January 2019 Through April 2019 For About $20.
Target Recalls Toddler Boots Due to Choking Hazard
Consumer Products·29,000 affected·Jun 11, 2019
High RiskFDA
Life Technologies Corporation
StemPro¿ MSC SFM CTS"
Medical Devices·4,724 affected·Jun 11, 2019
High RiskFDA
Randox Laboratories, Limited
Human Assayed Multi-Sera Level 2, Model NO. HN1530 Product Usage: This product is intended for in vitro diagnostic use, in the qualit...
Diagnostic Devices·149 affected·Jun 11, 2019
Medium RiskFDA
Tate & Lyle Ingredients Americas, Llc
Food starch, brand names Miraqk Mgl and Nustar 120 and Nustar 140
Food·128,850 affected·Jun 10, 2019
High RiskFDA
Preferred Pharmaceuticals, Inc
Robafen DM, Generic for Robitussin DM, In each teaspoonful (5mL): Dextromethorphan HBr, USP 10mg,/Guaifenesin, USP 100mg, 118mL (4oz) bot...
Drugs·192 affected·Jun 10, 2019
High RiskFDA
Philips Medical Systems (cleveland) Inc
BrightView XCT , Model Number 882482
Medical Devices·427 affected·Jun 10, 2019
High RiskFDA
Zimmer Biomet, Inc.
Comprehensive Reverse Shoulder Instrument Case Total (Outer Case Vault Only), Item Number 595510
Medical Devices·1,257 affected·Jun 10, 2019
High RiskFDA
Abbott Gmbh & Co. Kg
Alinity ci -series System Control¿Module, Part Number 03R70 01 Product Usage: The Alinity ci series System Control Module has a scala...
Diagnostic Devices·1,763 affected·Jun 10, 2019
RecallFDA
Randox Laboratories, Limited
Assayed Bovine Multi-Sera Level 1, Model No. AL1027
Diagnostic Devices·4 affected·Jun 10, 2019
High RiskFDA
Philips Medical Systems (cleveland) Inc
BrightView SPECT, Model Number 882480
Medical Devices·696 affected·Jun 10, 2019
High RiskFDA
Zimmer Biomet, Inc.
Comprehensive Reverse Shoulder Instrument Case Outer (Outer Case Vault Only), Item Number 595509
Medical Devices·92 affected·Jun 10, 2019
High RiskFDA
Molded Products Inc
Luer Lock Set - Catalog # MPC-125, for IV administration sets.
Medical Devices·130,000 affected·Jun 10, 2019
High RiskFDA
Philips Medical Systems (cleveland) Inc
BrightView X , Model Number 882478
Medical Devices·117 affected·Jun 10, 2019
RecallUSDA
Taylor Farms Illinois, Inc
Taylor Farms Illinois, Inc. Recalls Bacon Quiche Products due to Misbranding and Undeclared Allergens
Pork·0 affected·Jun 9, 2019
RecallUSDA
Taylor Farms Illinois, Inc
Taylor Farms Illinois, Inc. retira productos de quiche de tocineta debido a un error de rotulación y alérgenos no declarados
Pork·0 affected·Jun 9, 2019
CriticalFDA
The Kroger Co
PRIVATE SELECTION FROZEN TRIPLE BERRY MEDLEY, 16 oz
Produce·192 affected·Jun 7, 2019