Hazard Type

Crash Hazard Recalls

1,899 product recalls involving crash hazard. Search official CPSC, FDA, and USDA datasets for every recall issued due to this hazard.

1,899Total Recalls
90Critical
276.7MUnits Affected
All Recalls

Every Crash Hazard Recall

Sorted by most recent. Click any recall for full details and safety information.

1,899 recalls
High RiskFDA
Shimadzu Medical Systems
Bransist Safire, Digital Angiography System containing a MS-200 Ceiling Suspended C-arm Support - Product Usage: designed to provide fluo...
Surgical Devices·7 affected·Nov 18, 2020
High RiskFDA
Medtronic Inc., Cardiac Rhythm And Heart Failure (crhf)
Medtronic Cobalt DR MRI SureScan DDPB3D1, MR Conditional implantable dual chamber cardioverter defibrillator with SureScan technology and...
Medical Implants·2 affected·Nov 15, 2020
High RiskFDA
Medtronic Inc., Cardiac Rhythm And Heart Failure (crhf)
Medtronic Cobalt HF CRT-D MRI SureScan DTPB2D1, MR Conditional implantable cardioverter defibrillator with cardiac resynchronization ther...
Medical Implants·2 affected·Nov 15, 2020
High RiskFDA
Chromsystems Instruments & Chemicals Gmbh
MassChrom Amino Acid Analysis Plasma Control Level I, Order No. 0471 - Product Usage: The kit is intended for amino acid metabolic screen...
Medical Devices·362 affected·Nov 2, 2020
High RiskFDA
Chromsystems Instruments & Chemicals Gmbh
3PLUS1 Multilevel Plasma Calibrator Set, Order No. 75128 - Product Usage: The kit is intended for amino acid metabolic screening, confirm...
Medical Devices·200 affected·Nov 2, 2020
RecallCPSC
Cfmoto Dealers Nationwide From June 2020 Through September 2020 For About $13,000.
CFMOTO Recalls Recreational Off-Highway Vehicles Due to Crash Hazard (Recall Alert)
Vehicles / Atvs·627 affected·Sep 24, 2020
RecallCPSC
Residential Elevators' Dealers And Home Builders Nationwide From January 2014 Through April 2017 For Between $18,000 And $50,000.
Residential Elevators Recalls Elevators Due to Impact Hazard (Recall Alert)
Consumer Products·6,300 affected·Sep 10, 2020
RecallCPSC
Online At Spinlife.com, Scootaround.com, Accessnsm.com And Topmobility.com And Other Online Retailers From November 2017 Through September 2019 For About $4,500.
WHILL Recalls WHILL Personal Electric Vehicles Due to Crash and Injury Hazards
Vehicles / Atvs·1,160 affected·Sep 9, 2020
Medium RiskCPSC
Polaris, Kawasaki And Can-am Dealerships Nationwide From April 2014 Through May 2020 For Between $160 And $240 For Sub-zero And Between $250 And $550 For Click6 Harnesses. Polaris Dealerships Installed The Harnesses In Polaris Model Year 2015 And 2017-2020 Rzr Xp1000, Rzr Turbo, Rzr Turbos, And Rzr Pro Xp Utvs.
IMMI Recalls Harnesses Made for Polaris, Can-Am, and Kawasaki UTVs Due to Injury Hazard
Consumer Products·162,000 affected·Sep 2, 2020
High RiskFDA
Medline Industries Inc
Central Line Dressing Change Tray
Medical Devices·60 affected·Aug 12, 2020
RecallCPSC
Polaris Dealers Nationwide From September 2019 Through April 2020 For Between $14,600 And $26,300.
Polaris Recalls Ranger Off-Road Vehicles and PRO XD and Bobcat Utility Vehicles Due to Crash Hazard (Recall Alert)
Vehicles / Atvs·13,200 affected·Jul 23, 2020
RecallCPSC
Polaris Dealers Nationwide From November 2017 Through April 2020 For Between $3,800 And $4,200.
Polaris Recalls Phoenix 200 All-Terrain Vehicles ATVs Due to Crash Hazard (Recall Alert)
Vehicles / Atvs·2,800 affected·Jul 2, 2020
RecallCPSC
Polaris Dealers Nationwide From June 2018 Through March 2020 For Between $15,890 And $29,000.
Polaris Recalls Ranger and General Utility Vehicles Due to Crash Hazard (Recall Alert)
Vehicles / Atvs·26,730 affected·Jul 2, 2020
RecallCPSC
Authorized Honda Powersports Dealers Nationwide, From November 2018 Through March 2020, For Between $15,000 And $24,000.
Recreational Off-Highway Vehicles Recalled by American Honda Due to Crash and Injury Hazards (Recall Alert)
Vehicles / Atvs·25,000 affected·Jun 18, 2020
High RiskFDA
Medtronic Navigation, Inc.
StealthStation" S7 System with Polaris Spectra Camera part number PSU 9733437 - Product Usage: are intended as an aid for precisely locat...
Medical Devices·2 affected·Jun 5, 2020
RecallFDA
Somerset Therapeutics Llc
Brimonidine Tartrate Opthalmic Solution 0.2%, 10 mL bottle, Rx only, Manufactured for: Somerset Therapeutics, LLC Hollywood, FL 33024. Ma...
Drugs·48,852 affected·Jun 4, 2020
RecallFDA
Somerset Therapeutics Llc
Brimonidine Tartrate Opthalmic Solution 0.2%, 15 mL bottle, Rx only, Manufactured for: Somerset Therapeutics, LLC Hollywood, FL 33024. Ma...
Drugs·22,788 affected·Jun 4, 2020
Medium RiskFDA
Somerset Therapeutics Llc
Brimonidine Tartrate Opthalmic Solution 0.2%, 5 mL bottle, Rx only, Manufactured for: Somerset Therapeutics, LLC Hollywood, FL 33024. Mad...
Drugs·383,437 affected·Jun 4, 2020
High RiskFDA
Medtronic Inc., Cardiac Rhythm And Heart Failure (crhf)
Percepta CRT-P MRI, Model Numbers: a) W1TR01, b) W1TR04, c) W4TR01, d) W4TR04
Medical Devices·37,360 affected·Jun 4, 2020
High RiskFDA
Medtronic Inc., Cardiac Rhythm And Heart Failure (crhf)
CareLink SmartSync Device Manager, Model Number 24970A
Medical Devices·2,773 affected·Jun 4, 2020
High RiskFDA
Medtronic Inc., Cardiac Rhythm And Heart Failure (crhf)
Azure S DR MRI, Model Number W3DR01
Medical Devices·49,513 affected·Jun 4, 2020
High RiskFDA
Medtronic Inc., Cardiac Rhythm And Heart Failure (crhf)
Azure XT DR MRI, Model Numbers: a) W1DR01 and b) W2DR01
Medical Devices·266,252 affected·Jun 4, 2020
High RiskFDA
Medtronic Inc., Cardiac Rhythm And Heart Failure (crhf)
Azure S SR MRI, Model Number W3SR01
Medical Devices·11,953 affected·Jun 4, 2020
High RiskFDA
Medtronic Inc., Cardiac Rhythm And Heart Failure (crhf)
Azure XT SR MRI, Model Numbers: a) W1SR01 and b) W2SR01
Medical Devices·31,736 affected·Jun 4, 2020
High RiskFDA
Medtronic Inc., Cardiac Rhythm And Heart Failure (crhf)
Patient Connector, Model Number 24967
Medical Devices·1,025 affected·Jun 4, 2020
High RiskFDA
Medtronic Inc., Cardiac Rhythm And Heart Failure (crhf)
Serena CRT-P MRI, Model Numbers: a) W1TR02, b) W1TR05, c) W4TR02, d) W4TR05
Medical Devices·17,750 affected·Jun 4, 2020
CriticalFDA
Arrow International Inc
Arrow AutoCAT2 Intra-Aortic Balloon Pump AUTOCAT2 WAVE, Product Code IAP-0500
Medical Devices·2,123 affected·May 20, 2020
CriticalFDA
Arrow International Inc
Arrow AC3 Optimus Intra-Aortic Balloon Pump AC3 Optimus IABP NA/AJLA, Product Code IAP-0701
Medical Devices·2,123 affected·May 20, 2020
CriticalFDA
Arrow International Inc
Arrow AutoCAT2 Intra-Aortic Balloon Pump AUTOCAT2 WAVE JAPANESE, Product Code IAP-0500J
Medical Devices·2,123 affected·May 20, 2020
CriticalFDA
Arrow International Inc
Arrow AutoCAT2 Intra-Aortic Balloon Pump AUTOCAT 2, Product Code IAP-0400
Medical Devices·2,123 affected·May 20, 2020
CriticalFDA
Arrow International Inc
Arrow AutoCAT2 Intra-Aortic Balloon Pump AUTOCAT2 WAVE DUTCH, Product Code IAP-0500NL
Medical Devices·2,123 affected·May 20, 2020
CriticalFDA
Arrow International Inc
Arrow AutoCAT2 Intra-Aortic Balloon Pump AUTOCAT2 WAVE ITALIAN, Product Code IAP-0500I
Medical Devices·2,123 affected·May 20, 2020
High RiskFDA
Roi Cps Llc
Respirator Crash Cart Kit
Respiratory Devices·200 affected·May 19, 2020
High RiskFDA
Resource Optimization & Innovation Llc
Regard SRHS Central Line Kit, Sterile, 20/case - Product Usage: The Saline Flush Syringes are intended to be used only for the flushing o...
Medical Devices·12,640 affected·May 4, 2020
High RiskFDA
Becton Dickinson & Company
BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535
Medical Devices·16,099,310 affected·Apr 16, 2020
RecallCPSC
Authorized Yeti Snowmx Dealers From October 2017 Through February 2020 For About $8,600.
Camso Recalls Yeti SnowMX Conversion Kits Due to Crash Hazard
Consumer Products·380 affected·Apr 9, 2020
High RiskFDA
Skeletal Kinetics, Llc
OSTEOVATION EX, 5CC, IMPACT FORMULA. Product Number: 390-0205, UDI: 813845020047 - Product Usage: Callos is indicated to fill bony voids...
Surgical Devices·88 affected·Apr 6, 2020
High RiskFDA
Skeletal Kinetics, Llc
OSTEOVATION, 5CC, IMPACT FORMULA. Product Number: 390-2105, UDI: 813845020085 - Product Usage: Callos is indicated to fill bony voids or...
Surgical Devices·1,393 affected·Apr 6, 2020
High RiskFDA
Skeletal Kinetics, Llc
CRANIOSCULPT, CMF IMPACT, 3CC Product Number: C-CMF3CC, UDI: 813845020931 - Product Usage: Callos is indicated to fill bony voids or gap...
Surgical Devices·27 affected·Apr 6, 2020
High RiskFDA
Skeletal Kinetics, Llc
CRANIOSCULPT, CMF IMPACT, 10CC, Product Number: C-CMF10CC, UDI: 813845020955 - Product Usage: Callos is indicated to fill bony voids or ...
Surgical Devices·51 affected·Apr 6, 2020
High RiskFDA
Skeletal Kinetics, Llc
OSTEOVATION IMPACT 10CC and OSTEOVATION, 10CC, IMPACT FORMULA, Product Number: 390-2110, UDI: 813845020092 - Product Usage: Callos is in...
Surgical Devices·661 affected·Apr 6, 2020
High RiskFDA
Skeletal Kinetics, Llc
CRANIOSCULPT, CMF IMPACT, 5CC, Product Number: C-CMF5CC, UDI: 813845020948 - Product Usage: Callos is indicated to fill bony voids or ga...
Surgical Devices·32 affected·Apr 6, 2020
High RiskFDA
Osteomed, Llc
OSTEOVATION 5CC IMPACTFORMULA. REF/UDI: 390-2105/00813845020085 - Product Usage: The product provides a bone void filler that is replaced...
Medical Devices·1,724 affected·Apr 2, 2020
High RiskFDA
Osteomed, Llc
OSTEOVATION 10 CC IMPACT FORMULA. REF/UDI: 390-2110/ /00813845021092 - Product Usage: The product provides a bone void filler that is rep...
Medical Devices·995 affected·Apr 2, 2020
High RiskFDA
Glaxosmithkline Consumer Healthcare Holdings
Advil Sinus Congestion and Pain/Advil Allergy and Congestion Relief 8 pc with $1 IRC (mixed product display - only Advil Allergy & Conges...
Drugs·566 affected·Mar 16, 2020
High RiskFDA
Abbott Gmbh & Co. Kg
ARCHITECT HAVAB G Reagent Kit. List Number 6L27 25.
Diagnostic Devices·7,347 affected·Mar 9, 2020
High RiskFDA
Haemonetics Corporation
TEG Manager software versions used in conjunction with TEG 5000 are 1.1.0, 3.0.0, 4.0.0, 4.1.0 and 4.1.1. Intended: For in vitro coagul...
Medical Devices·88 affected·Feb 19, 2020
RecallCPSC
Bobcat Dealers Nationwide From May 2016 Through February 2019 For Between $24,000 And $29,000.
Bobcat Company Recalls Utility Vehicles (UTVs) Due to Collision and Crash Hazard (Recall Alert)
Vehicles / Atvs·522 affected·Jan 30, 2020