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All Product Recalls

78,569 recalls

Source:AllCPSCFDAUSDASeverity:AllCriticalHighMedium
High RiskFDA
Ion Beam Applications S.a.
Proteus 235, Pencil Beam Scanning version PTS-6.4.11.X The Proton Therapy System - Proteus 235 (brand names: Proteus Plus and Proteus ...
Medical Devices·3 affected·Oct 19, 2017
High RiskFDA
Datascope Corporation
BEQ-TOP 27610 ECC PACK 3/8, Custom Tubing Kit, Catalog No. 701065622
Medical Devices·9 affected·Oct 19, 2017
High RiskFDA
Cook Inc.
Mallinckrodt Institute Percutaneous Gastrostomy Set Product Usage: Intended for the percutaneous placement of a catheter for gastro...
Surgical Devices·615 affected·Oct 19, 2017
High RiskFDA
Datascope Corporation
BEQ-TOP 22301, Custom Tubing Kit, Catalog No. 701049513
Medical Devices·1 affected·Oct 19, 2017
High RiskFDA
Johnson & Johnson Vision Care, Inc.
ACUVUE OASYS Brand Contact Lenses with HYDRACLEAR PLUS
Medical Devices·125,763 affected·Oct 19, 2017
High RiskFDA
Datascope Corporation
BEQ-TOP 33700 ECC 3/8" PACK, Custom Tubing Pack with Bioline Coating, Catalog No. 701053845
Medical Devices·22 affected·Oct 19, 2017
High RiskFDA
Datascope Corporation
Adult ECC Pack BEQ-TOP 22300, Catalog No. 701049504
Medical Devices·3 affected·Oct 19, 2017
High RiskFDA
Datascope Corporation
BO-TOP 13901 RAPID RESPONSE, Custom Tubing Kit, Catalog No. 701054874
Medical Devices·11 affected·Oct 19, 2017
High RiskFDA
Datascope Corporation
ECC Small - Respiratory BEQ-TOP 5210, Custom Tubing Kit, Catalog No. 701055604
Respiratory Devices·4 affected·Oct 19, 2017
High RiskFDA
Cook Inc.
Percutaneous Gastrojejunostomy Set Product Usage: Intended for the percutaneous placement of a catheter for gastroenteric feeding
Surgical Devices·1 affected·Oct 19, 2017
High RiskFDA
Datascope Corporation
BO-TOP 20700 SMALL PATIENT 3/8, Custom Tubing Kit, Catalog No. 701050966
Medical Devices·4 affected·Oct 19, 2017
High RiskFDA
Datascope Corporation
BEQ-TOP 5210 ECC Set - Respiratory, Custom Tubing Kit, Catalog No. 701055604R01
Respiratory Devices·18 affected·Oct 19, 2017
High RiskFDA
Datascope Corporation
BEQ-TOP 22701, Catalog No. 701050790
Medical Devices·4 affected·Oct 19, 2017
High RiskFDA
Datascope Corporation
BEQ-TOP 38900 ECC PACK, Custom Tubing Kit, Catalog No. 701056368
Medical Devices·9 affected·Oct 19, 2017
High RiskFDA
Datascope Corporation
BEQ-T 25502 1/4 Better Bladder , Custom Tubing Kit, Catalog No. 709000434
Medical Devices·40 affected·Oct 19, 2017
High RiskFDA
Datascope Corporation
BEQ-TOP 49101 Childrens Large ECC Pack, Custom Tubing Kit, Catalog No. 701067069R01
Medical Devices·4 affected·Oct 19, 2017
High RiskFDA
Datascope Corporation
NICU ECC Pack BEQ-TOP 39202, Custom Tubing Kit, Catalog No. 701067313R01
Medical Devices·3 affected·Oct 19, 2017
High RiskFDA
Datascope Corporation
BO-TOP 20705 SMALL PATIENT 1/4, Catalog No. 701053486
Medical Devices·10 affected·Oct 19, 2017
High RiskFDA
Datascope Corporation
BEQ-TOP 41201 ECC 3/8 PUMP PAC, Custom Tubing Kit, Catalog No. 701064867
Medical Devices·18 affected·Oct 19, 2017
High RiskFDA
Johnson & Johnson Vision Care, Inc.
1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses
Medical Devices·56,070 affected·Oct 19, 2017
High RiskFDA
Datascope Corporation
BEQ-TOP 24500 ADULT ECC, Custom Tubing Kit, Catalog No. 701050253
Medical Devices·4 affected·Oct 19, 2017
High RiskFDA
Datascope Corporation
BEQ-T 9410 Lurie Chldns Small 1/4, Custom Tubing Kit, Catalog No. 709000430
Medical Devices·6 affected·Oct 19, 2017
High RiskFDA
Datascope Corporation
BEQ-TOP 25500 ECC 3/8 w/QiD, Custom Tubing Kit, Catalog No. 701052461
Medical Devices·18 affected·Oct 19, 2017
High RiskFDA
Datascope Corporation
BEQ-TOP 24202 ADULT ECC, Catalog No. 701054295
Medical Devices·9 affected·Oct 19, 2017
High RiskFDA
Datascope Corporation
BEQ-TOP 40700 HUNTINGTON, Catalog No. 701062899
Medical Devices·4 affected·Oct 19, 2017
High RiskFDA
Cook Inc.
Wills-Oglesby Percutaneous Gastrostomy Set Product Usage: Intended for the percutaneous placement of a catheter for gastroenteric feeding
Surgical Devices·1 affected·Oct 19, 2017
High RiskFDA
Datascope Corporation
BEQ-TOP 8504 1/4X1/4 PACK W/QP, Custom Tubing Kit, Catalog No. 701066949R02
Medical Devices·10 affected·Oct 19, 2017
CriticalFDA
Myanmar Wholesale Trading
Thanlwin Fried Bean Snack, Net Weight 227 g 8 oz.. UPC 84682-00095 Product of Myanmar.
Snacks & Candy·92 affected·Oct 18, 2017
High RiskFDA
Bioseal Corporation
Custom surgical kits labeled as follows: (a) Suture Removal Set, 910-0002 (b) Instrument Set, INST03/20 (c) Suture Removal Set, SUT309...
Surgical Devices·51,635 affected·Oct 18, 2017
RecallUSDA
Unknown
Les Chateaux De France, Inc. Recalls Bacon-Wrapped Scallops due to Misbranding and an Undeclared Allergen
Pork·0 affected·Oct 18, 2017
RecallUSDA
Unknown
Les Chateaux De France, Inc. Retira Productos De Callo De Hacha o Vieira ("Scallops") Envueltos En Tocino Debido A Un Error De Rotulación Y Alérgeno No Declarado
Pork·0 affected·Oct 18, 2017
RecallCPSC
John Deere Dealers Nationwide From July 2017 Through August 2017 For Between $3,800 And $8,000.
Frontier Wood Chippers Recalled by John Deere Due to Injury Hazard
Consumer Products·25 affected·Oct 17, 2017
RecallCPSC
Herman Miller, Design Within Reach And Herman Miller's Authorized Retailers And Dealers Nationwide And Online At Http://store.hermanmiller.com And Www.dwr.com From May 2013 Through September 2017 For About $650 (non-upholstered) And $890 (upholstered).
Herman Miller Recalls Fiberglass Rocking Chairs Due to Fall Hazard
Furniture·1,600 affected·Oct 17, 2017
CriticalCPSC
Polaris Dealers Nationwide From December 2014 Through July 2017 For About $7,500.
Polaris Recalls ACE 325 Recreational Off-Highway Vehicles Due to Fire and Burn Hazards
Vehicles / Atvs·6,300 affected·Oct 17, 2017
RecallCPSC
Target Stores Nationwide And Online From June 2017 Through August 2017 For About $35.
Target Recalls Leather Pouf Ottoman Due to Suffocation and Choking Hazards
Consumer Products·7,500 affected·Oct 17, 2017
CriticalFDA
Weis Markets, Inc., Ice Cream Division
Weis, Sunbury, PA; BLT Sandwich; 1 CT
Food·452 affected·Oct 17, 2017
CriticalFDA
Stonyfield Farm
Stonyfield ORGANIC O'soy Strawberry on the bottom SOY YOGURT 5.3 Oz (150g), UPC Codes: 0-52159-00603-7. KEEP REFRIGERATED
Dairy·17,688 affected·Oct 17, 2017
RecallFDA
Teva Pharmaceuticals Usa
Methylphenidate Hydrochloride Tablets USP, 20 mg, 100-count bottles, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA 928...
Oral Drugs·58,292 affected·Oct 17, 2017
High RiskFDA
Arrow International Inc
Pressure Injectable Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter and Sharps Safety Features; Product Code...
Surgical Devices·5,926 affected·Oct 17, 2017
High RiskFDA
Arrow International Inc
ARROWg+ard Blue Plus Multi Lumen CVC (Central venous catheter); Product Code: AK-45703-ACDC; Exp. Dates Feb 2018 - Nov 2018
Surgical Devices·5,926 affected·Oct 17, 2017
High RiskFDA
Arrow International Inc
Arrow Multi Lumen CVC Kit (Central venous catheter); Product Code: CDC-15703-1A; Exp. Dates Feb 2018 - Nov 2018
Surgical Devices·5,926 affected·Oct 17, 2017
High RiskFDA
3m Company - Health Care Business
3M Bair Hugger(TM) Normothermia System, Temperature Monitoring System Sensors Model 360 (Part Number 36000)
Medical Devices·153 affected·Oct 17, 2017
High RiskFDA
Arrow International Inc
ARROWg+ard Blue Two Lumen Hemodialysis Catheterization Kit for High Volume Infusions; Product Codes: AK-22142-CDC, AK-22142-F, AK-25142-C...
Surgical Devices·5,926 affected·Oct 17, 2017
High RiskFDA
Siemens Healthcare Diagnostics
BC Thrombin Reagent Kit Lot Number 46751; UDI - 008427680131024675120180908 and BC Thrombin Reagent Kit Lot Number 47184; UDI -00842768...
Diagnostic Devices·7,631 affected·Oct 17, 2017
High RiskFDA
Arrow International Inc
Multi Lumen Central Venous Catheterization Kit; Product Code: ASK-12703-HH2; Exp. Dates Feb 2018 - Nov 2018
Surgical Devices·5,926 affected·Oct 17, 2017
High RiskFDA
Southmedic, Inc.
Southmedic Oxygen Masks with EtCO2 sampling line part number OM-2125-8, 25 masks per case. Minimal contact, open oxygen delivery devic...
Respiratory Devices·8,871 affected·Oct 17, 2017
High RiskFDA
Ion Beam Applications S.a.
Proteus 235, graphite block 8
Medical Devices·3 affected·Oct 17, 2017
High RiskFDA
Arrow International Inc
Central Venous Catheterization Kit with Blue FlexTip Catheter; Product code: AK-04301; Exp. Dates Feb 2018 - Nov 2018
Surgical Devices·5,926 affected·Oct 17, 2017