Year

2017 Product Recalls

6,210 product recalls issued in 2017 across CPSC, FDA, and USDA datasets.

6,210 recalls
High RiskFDA
Prosupps Usa Llc
Dr. Jekyll V2 Mango Passion Fruit Domestic 30; Dr. Jekyll Mango Passion Fruit V2 domestic
Produce·2,508 affected·Aug 30, 2017
High RiskFDA
Prosupps Usa Llc
Hyde V2 Cherry Bomb
Food·4,483 affected·Aug 30, 2017
High RiskFDA
Prosupps Usa Llc
DNPX Powder, 30 Green Apple
Food·694 affected·Aug 30, 2017
High RiskFDA
Prosupps Usa Llc
Dr. Jekyll Green Apple V2 domestic
Food·1,827 affected·Aug 30, 2017
High RiskFDA
Prosupps Usa Llc
Hyde V2 Watermelon; Mr. Hyde V2 Watermelon International 30; Mr. Hyde V2 Watermelon Domestic 60
Beverages·22,505 affected·Aug 30, 2017
High RiskFDA
Prosupps Usa Llc
Mr. Hyde Fruit Punch Canada; Mr. Hyde V2 Fruit Punch domestic
Produce·30,842 affected·Aug 30, 2017
High RiskFDA
Prosupps Usa Llc
Vanish V3
Food·573 affected·Aug 30, 2017
High RiskFDA
Prosupps Usa Llc
Hyde V2 Berry Blast
Produce·3,803 affected·Aug 30, 2017
High RiskFDA
Prosupps Usa Llc
DNPX Powder, 30 Pineapple Punch
Food·40 affected·Aug 30, 2017
High RiskFDA
Prosupps Usa Llc
Dr. Jekyll V2 international Blue Razz sample packs, Dr. Jekyll Blue Razz V2 domestic
Food·3,727 affected·Aug 30, 2017
High RiskFDA
Prosupps Usa Llc
Hyde V2 Orange Burst
Food·2,147 affected·Aug 30, 2017
High RiskFDA
Prosupps Usa Llc
Mr. Hyde Green Apple domestic sample pack
Food·25,318 affected·Aug 30, 2017
RecallFDA
Lipari Foods, Inc.
Sunflower Seeds Honey Roasted, 12oz Tubs & 25lb Bulk
Food·702 affected·Aug 30, 2017
High RiskFDA
Prosupps Usa Llc
DNPX Powder, 30 Blue Razz
Food·2 affected·Aug 30, 2017
High RiskFDA
Prosupps Usa Llc
Dr. Jekyll V2 Orange Burst Domestic 30; Dr. Jekyll Orange Burst domestic sample packs
Food·65,195 affected·Aug 30, 2017
High RiskFDA
Mid Valley Pharmaceutical
Doctor Manzanilla Allergy & Decongestant Relief (diphenhydramine hydrochloride and phenylephrine hydrochloride) Syrup, 12.5 mg and 5 mg ...
Drugs·24 affected·Aug 30, 2017
CriticalFDA
Pfizer Inc.
Vancomycin Hydrochloride for Injection, USP. 750 mg. Sterile Powder. Rx Only. Hospira, Inc., Lake Forest, IL 60045 USA. NDC: 0409-6531-02
Injectable Drugs·102,500 affected·Aug 30, 2017
High RiskFDA
Noven Pharmaceuticals, Inc.
Daytrana (methylphenidate transdermal system) Delivers 30 mg over 9 hours (3.3 mg/hr) Rx Only Contains: 30 Patches Manufactured for: Nov...
Topical Drugs·331,950 affected·Aug 30, 2017
High RiskFDA
Noven Pharmaceuticals, Inc.
Daytrana (methylphenidate transdermal system) Delivers 20 mg over 9 hours (2.2 mg/hr) Rx Only Contains: 30 Patches Manufactured for: Nov...
Topical Drugs·182,850 affected·Aug 30, 2017
High RiskFDA
Mid Valley Pharmaceutical
Doctor Manzanilla Cough & Cold (diphenhydramine hydrochloride and phenylephrine hydrochloride) Syrup, 12.5 mg and 5 mg in each 5 mL, 4 fl...
Drugs·24 affected·Aug 30, 2017
High RiskFDA
Noven Pharmaceuticals, Inc.
Daytrana (methylphenidate transdermal system) Delivers 15 mg over 9 hours (1.6 mg/hr) Rx Only Contains: 30 Patches Manufactured for: Nov...
Topical Drugs·234,960 affected·Aug 30, 2017
High RiskFDA
Noven Pharmaceuticals, Inc.
Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Rx Only Contains: 30 Patches Manufactured for: Nov...
Topical Drugs·321,900 affected·Aug 30, 2017
High RiskFDA
Carl Zeiss Meditec Ag
Carl Zeiss INTRABEAM PRS 500, product #304534-0000-500. The firm name on the label is Carl Zeiss Meditec AG, Jena, Germany. The INTRABE...
Medical Devices·9 affected·Aug 30, 2017
RecallUSDA
Unknown
Demakes Enterprises, Inc. Recalls Chicken Sausage Product Due To Misbranding and Undeclared Allergens
Pork·0 affected·Aug 30, 2017
RecallUSDA
Unknown
Demakes Enterprises, Inc. Retira Productos De Salchicha De Pollo Debido A Un Error De Rotulacion Y Alérgeno No Declarado
Pork·0 affected·Aug 30, 2017
RecallCPSC
Cracker Barrel Old Country Store Stores Nationwide From April 2017 Through July 2017 For About $20.
Fabri-Tech Recalls Infant Rompers Due to Choking Hazard; Sold Exclusively at Cracker Barrel Old Country Stores
Children's Products·6,500 affected·Aug 29, 2017
CriticalFDA
Lucky Mart Inc.
PIYANPING Anti-Itch (hydrocortisone) Lotion, 1%, Net Wt. 0.67 oz (20g) tube, Manufactured By: Jimin Pharmaceutial Co., LTD., Distributor:...
Drugs·13,800 affected·Aug 29, 2017
RecallFDA
Amerisource Health Services
Enalapril Maleate Tablets, USP, 5 mg, 100 Tablets (10 x 10), Rx Only. Packaged and Distributed by: American Health Packaging, Columbus,...
Oral Drugs·93,600 affected·Aug 29, 2017
High RiskFDA
Becton Dickinson & Company
BD Vacutainer¿ K2 EDTA (K2E) 3.6mg Blood Collection Tube (13 x 75 mm x 2.0 mL). Catalog Number: 367841. Used for whole blood hematolo...
Medical Devices·8,494,000 affected·Aug 29, 2017
High RiskFDA
Gonzalez Wholesale Distributor,l
Primera Negra, Artificial Vanilla Flavoring NET WT 4 OZ and 8 OZ
Food·25 affected·Aug 28, 2017
High RiskFDA
Bateman Community Living
Breaded Fish with Vera Cruz Sauce; In 13.4 oz 3 compartment tray that has the fish, rice pilaf and green peas. Item number KD-0003 No ...
Seafood·8,792 affected·Aug 28, 2017
High RiskFDA
Tomanetti Food Products Inc
12" homestyle pizza crusts packed 18 to a case (no consumer packaging) labeled as: Tomanetti Pizza Crusts with the 18-12" Homestyle 9111...
Frozen Food·132 affected·Aug 28, 2017
RecallFDA
Mckesson Packaging Services
Propafenone Hydrochloride tablets, 150 mg, packaged in 10 x 10 unit dose cards (100-count box), Rx only, Manufactured By: Watson Pharmace...
Oral Drugs·3,966 affected·Aug 28, 2017
High RiskFDA
St Jude Medical Inc.
Assurity MRI Model Numbers: PM1272, PM2272 Implantation of a single-chamber pulse generator, dual-chamber pulse generator, or CRT-P is i...
Medical Implants·164,366 affected·Aug 28, 2017
High RiskFDA
St Jude Medical Inc.
PM1226 ACCENT ST MRI SR RF and PM2222 ACCENT ST These low voltage (LV) devices are implantable pacemaker pulse generators, intended to b...
Medical Implants·101 affected·Aug 28, 2017
High RiskFDA
St Jude Medical Inc.
Assurity Model Numbers: PM1240, PM2240; Assurity + Model Number: PM2260; Accent Model Numbers: PM1210, PM2210, PM1222, PM2212; Accent MRI...
Medical Implants·529,912 affected·Aug 28, 2017
High RiskFDA
Zimmer Biomet, Inc.
Persona Partial Knee System Product Usage: The Persona Partial Knee System instruments are used by a surgeon to facilitate the implan...
Medical Implants·1,275 affected·Aug 28, 2017
High RiskFDA
St Jude Medical Inc.
Merlin@Home Software Model EX2000 v8.2.2 for Merlin@Home Transmitter Models EX1150, EX1150W, EX1100, and EX1100W. The Merlin@home Transm...
Medical Implants·495,011 affected·Aug 28, 2017
High RiskFDA
St Jude Medical Inc.
PM1214 NUANCE SR RF; PM1230 and PM2230 NUANCE MRI; PM2214 NUANCE DR RF These low voltage (LV) devices are implantable pacemaker pulse ge...
Medical Implants·2,741 affected·Aug 28, 2017
High RiskFDA
St Jude Medical Inc.
Merlin PCS 3650 Programmer with Model 3330 Software Version 23.1.1 The Merlin Patient Care System (PCS) Model 3650 Programmer is a porta...
Medical Implants·10,453 affected·Aug 28, 2017
High RiskFDA
St Jude Medical Inc.
Anthem Model Numbers: PM3210, PM3212; Allure/Relieve Model Numbers: PM3222, PM3242, PM3262, PM3542, PM3224, PM3244 Implantation of a sin...
Medical Implants·102,684 affected·Aug 28, 2017
RecallUSDA
Unknown
Ronald A. Chisholm, Ltd. Recalls Pork Belly Products Produced Without Benefit of Import Inspection
Pork·0 affected·Aug 26, 2017
RecallUSDA
Unknown
Ronald A. Chisholm, Ltd. Retira Productos De Panza De Cerdo Producidos Sin El Beneficio De Inspección De Importación
Pork·0 affected·Aug 26, 2017
RecallUSDA
Blossom Foods, Llc
Blossom Foods, LLC Recalls Frozen Meat Products Due to Misbranding and Undeclared Allergens
Beef·0 affected·Aug 26, 2017
RecallUSDA
Blossom Foods, Llc
Blossom Foods, LLC Retira Productos De Carne Congelados Debido A Un Error De Rotulación Y Alérgenos No Declarados
Beef·0 affected·Aug 26, 2017
High RiskFDA
Biomerieux Inc
VITEK(R) 2 GP, REF 21342, IVD, UDI 03573026131920, bioMerieux, Inc. VITEK(R) 2 is an automated system consisting of instruments, softwar...
Medical Implants·11,703 affected·Aug 25, 2017
High RiskFDA
Zimmer Biomet, Inc.
G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for use in hip arthroplasty cases which involves the removal of the damaged joi...
Medical Implants·8 affected·Aug 25, 2017
High RiskFDA
Zimmer Biomet, Inc.
AGC 2000 LP Patella, labeled as AGC Porous Patellar SM, Model Number 150802. Product Usage: For use in Total Knee Arthroplasty.
Medical Devices·28 affected·Aug 25, 2017