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
Medtech Products, Inc.
Clear Eyes Assorted IRC Display; each display contains 6 each of a) Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoline hydrochloride ...
Ophthalmic Drugs·20,808 affected·Jul 26, 2019
High RiskFDA
Medtech Products, Inc.
Clear Eyes Assorted Sidekick Floor Stand Display; each display contains 6 each of a) Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoli...
Ophthalmic Drugs·25,992 affected·Jul 26, 2019
High RiskFDA
Medtech Products, Inc.
Clear Eyes Maximum Itchy Eye Relief Sidekick Floor Stand Display; each display (case UPC 10678112736383) contains 12 each of Clear eyes M...
Ophthalmic Drugs·1,836 affected·Jul 26, 2019
High RiskFDA
Medtech Products, Inc.
Clear Eyes Redness Relief Handy Pocket Pal Club Pak Display; each display (case UPC 30300742541283) contains 48 each of Clear eyes REDNES...
Ophthalmic Drugs·793,872 affected·Jul 26, 2019
High RiskFDA
Medtech Products, Inc.
Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.012%) eye drops, Handy Pocket Pal, 0.2 FL OZ (6 mL) bottle, Distri...
Ophthalmic Drugs·1,030,128 affected·Jul 26, 2019
High RiskFDA
Medtech Products, Inc.
Clear Eyes Redness Relief Club Pack Display; each display contains 18 3-Pack bottles (UPC 6 78112 10552 6) of Clear eyes REDNESS RELIEF (...
Ophthalmic Drugs·124,038 affected·Jul 26, 2019
High RiskFDA
Medtech Products, Inc.
Clear Eyes Maximum Redness Relief Club Pack Display; each display contains 18 3-Pack bottles (UPC 6 78112 10859 6) of Clear eyes MAXIMUM ...
Ophthalmic Drugs·17,316 affected·Jul 26, 2019
High RiskFDA
Medtech Products, Inc.
Clear Eyes Maximum Itchy Eye Relief Sidekick Floor Stand Display; each display contains 12 each of Clear eyes MAXIMUM ITCHY EYE RELIEF (G...
Ophthalmic Drugs·1,752 affected·Jul 26, 2019
High RiskFDA
Medtech Products, Inc.
Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.012%) eye drops, Handy Pocket Pal, 0.2 FL OZ (6 mL) bottle, Dist. ...
Ophthalmic Drugs·1,621,200 affected·Jul 26, 2019
High RiskFDA
Medtech Products, Inc.
Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.012%) eye drops, packaged in a) 0.5 FL OZ (15 mL) bottle (UPC 6 78...
Ophthalmic Drugs·6,661,188 affected·Jul 26, 2019
High RiskFDA
Medtech Products, Inc.
Clear eyes MAXIMUM REDNESS RELIEF (Glycerin 0.5%, Naphazoline hydrochloride 0.03%) eye drops, 0.5 FL OZ (15 mL) bottle, Distributed by Me...
Ophthalmic Drugs·1,872,984 affected·Jul 26, 2019
High RiskFDA
Medtech Products, Inc.
Clear Eyes Redness Relief Hand Pocket Pal Tray Display; each display (UPC 6 78112 25418 7) contains 48 each of Clear eyes REDNESS RELIEF ...
Ophthalmic Drugs·314,112 affected·Jul 26, 2019
High RiskFDA
Medtech Products, Inc.
Clear eyes MAXIMUM ITCHY EYE RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.012%, Zinc Sulfate 0.25%) eye drops, 0.5 FL OZ (15 mL) b...
Ophthalmic Drugs·927,108 affected·Jul 26, 2019
High RiskFDA
Medtech Products, Inc.
Clear Eyes Maximum Redness and Itchy Eye Relief Sidekick Display; each display contains 12 each of a) Clear eyes MAXIMUM REDNESS RELIEF (...
Ophthalmic Drugs·66,168 affected·Jul 26, 2019
High RiskFDA
Lemaitre Vascular, Inc.
The LeMaitre Aortic Occlusion Catheter is a single lumen catheter with a latex balloon, it is offered in two balloon sizes: 28 mm or 45mm...
Surgical Devices·62 affected·Jul 24, 2019
RecallCPSC
Master Spas Hot Tub/spa Distributors From December 2017 Through May 2019 For Between About $5000 And $45,000 And About $2 For The Valve Caps.
Custom Molded Products Recalls Valve Caps Sold With Hot Tubs/Swim Spas Due to Impact Hazard
Consumer Products·16,000 affected·Jul 10, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
SOMATOM Definition AS, Model Number 8098027 - Product Usage: Computed tomography systems intended to generate and process cross-sectional...
Medical Devices·0 affected·Jul 3, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
SOMATOM Drive, Model Number 10431700 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images...
Medical Devices·0 affected·Jul 3, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
SOMATOM Force, Model Number 10742326 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images...
Medical Devices·0 affected·Jul 3, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
SOMATOM Edge Plus, Model Number 10267000 - Product Usage: Computed tomography systems intended to generate and process cross-sectional im...
Medical Devices·0 affected·Jul 3, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
SOMATOM Definition Edge, Model Number 10590000 - Product Usage: Computed tomography systems intended to generate and process cross-sectio...
Medical Devices·0 affected·Jul 3, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
SOMATOM Definition Flash, Model Number 10430603 - Product Usage: Computed tomography systems intended to generate and process cross-secti...
Medical Devices·0 affected·Jul 3, 2019
RecallCPSC
Bicycles With The Recalled Forks Were Sold At Bicycle Stores Nationwide From January 2019 Through March 2019. Bicycle Forks Sold As Aftermarket Accessories Were Sold At Bicycle Stores From February 2019 Through April 2019 For Between $700 And $1,000.
SRAM Recalls RockShox Front Suspension Forks Due to Crash and Injury Hazards
Consumer Products·840 affected·Jul 2, 2019
RecallCPSC
Authorized Honda Powersports Dealers Nationwide From August 2015 Through March 2019 For Between $14,000 And $22,000.
American Honda Recalls Recreational Off-Highway Vehicles Due to Crash and Injury Hazards (Recall Alert)
Vehicles / Atvs·82,000 affected·Jun 13, 2019
RecallCPSC
Polaris Dealers Nationwide From February 2014 Through January 2019 For About $11,900.
Polaris Recalls Recreational Off Highway Vehicles Due to Crash Hazard (Recall Alert)
Vehicles / Atvs·3,900 affected·Jun 4, 2019
RecallCPSC
Polaris Dealers Nationwide From December 2017 Through January 2019 For About $28,400.
Polaris Recalls RZR Recreational Off-Highway Vehicles Due to Crash and Injury Hazards (Recall Alert)
Vehicles / Atvs·1,200 affected·Jun 4, 2019
RecallCPSC
Rei Stores And Bicycle Shops Nationwide And Online At Www.revelatedesigns.com From December 2018 Through April 2019 For About $160.
Revelate Designs Recalls Bicycle Seat Bags Due to Crash, Injury Hazards
Bicycles & Wheeled Sports·1,250 affected·May 23, 2019
RecallUSDA
Blount Fine Foods Corp.
Blount Fine Foods Recalls Soup with Chicken Products Due to Possible Foreign Matter Contamination
Poultry·0 affected·May 23, 2019
RecallCPSC
Textron Off Road And Arctic Cat Dealers Nationwide From January 2018 Through April 2019 For Between $13,800 And $17,000.
Arctic Cat Recalls Textron Recreational Off-Highway Vehicles Due to Crash Hazard (Recall Alert)
Vehicles / Atvs·1,700 affected·May 22, 2019
CriticalFDA
Medline Industries Inc
Centurion Convenience Kits, containing BD Alaris Pump Infusion Sets. BD code 11522558 (Centurion code 110931) contained inside kits DYNJ5...
Medical Devices·4,890 affected·May 10, 2019
RecallUSDA
Conagra Brands (conagra Foods Packaged Foods, Llc)
Conagra Brands, Inc. Recalls Chicken Pad Thai and Chicken Fried Rice Products Due to Misbranding and Undeclared Allergens
Poultry·0 affected·May 4, 2019
RecallCPSC
Ktm And Husqvarna Motorcycles Authorized Dealers Nationwide From March 2018 December 2018 For About $4,300.
KTM and Husqvarna Motorcycles Recall Motorcycles Due to Crash Hazard (Recall Alert)
Vehicles / Atvs·780 affected·Apr 10, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
Artis Zeego (material 10280959) - Product Usage: AXIOM Artis zee and Q/ Q.zen is a family of dedicated angiography systems developed for ...
Cardiac Devices·459 affected·Apr 9, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
Artis Q (material 10848280, 10848281, 10848282) - Product Usage: AXIOM Artis zee and Q/ Q.zen is a family of dedicated angiography system...
Cardiac Devices·459 affected·Apr 9, 2019
High RiskFDA
Siemens Medical Solutions Usa, Inc
Siemens Digital Linear Accelerators of type: ARTISTE MV System MEVATRON M2/Primus Mid-Energy PRIMUS PRIMUS HI ONCOR Impression ONCOR...
Medical Devices·120 affected·Mar 20, 2019
RecallCPSC
Stromer Authorized Dealers Nationwide From April 2018 Through February 2019 For About $10,000.
myStromer Recalls Electric Bicycles Due to Crash and Injury Hazards (Recall Alert)
Bicycles & Wheeled Sports·195 affected·Mar 19, 2019
RecallCPSC
Textron Off Road And Arctic Cat Dealers Nationwide From September 2017 Through December 2018 For Between $13,800 And $16,000.
Arctic Cat Recalls Textron Off-Highway Utility Vehicles Due to Crash Hazard (Recall Alert)
Vehicles / Atvs·700 affected·Mar 5, 2019
CriticalFDA
Brainlab Ag
Spine & Trauma 3D Navigation 1.0 (subpart of the system Navigation Software Spine & Trauma 3D, Version 3.0 ) Intended Use The Spine ...
Medical Devices·148 affected·Feb 27, 2019
RecallCPSC
Specialty Bicycle Retailers Nationwide From April 2010 Through December 2018 For Between $400 And $800 For Electra Bicycles Equipped With The Recalled Hubs And For About $90 For The Recalled Aftermarket Gear Hubs
SRAM Recalls Bicycle Gear Hubs Due to Crash and Injury Hazards
Bicycles & Wheeled Sports·7,000 affected·Feb 21, 2019
High RiskFDA
Luminex Corporation
ARIES HSV 1&2 Assay , REF 50-10017, UDI # 00840487100295
Diagnostic Devices·0 affected·Feb 20, 2019
High RiskFDA
Luminex Corporation
ARIES C. difficile Assay , REF 50-10018, UDI # 00840487100059
Diagnostic Devices·0 affected·Feb 20, 2019
High RiskFDA
Luminex Corporation
ARIES Flu A/B & RSV Assay , REF 50-10020, UDI # 00840487100158
Diagnostic Devices·0 affected·Feb 20, 2019
High RiskFDA
Luminex Corporation
ARIES GBS Assay , REF 50-10021, UDI # 00840487100165
Diagnostic Devices·0 affected·Feb 20, 2019
High RiskFDA
Luminex Corporation
ARIES Group A Strep Assay , REF 50-10041, UDI # 00840487101469
Diagnostic Devices·0 affected·Feb 20, 2019
High RiskFDA
Luminex Corporation
Aries Bordetella Assay, REF 50-10037, UDI # 00840487101452
Diagnostic Devices·0 affected·Feb 20, 2019
High RiskFDA
Abbott Ireland Diagnostics Division
Abbott ARCHITECT Estradiol Reagent Kit - Product Usage: The ARCHITECT Estradiol assay is a Chemiluminescent Microparticle Immunoassay (CM...
Diagnostic Devices·2,724 affected·Feb 5, 2019
High RiskFDA
Encore Medical, Lp
EMPOWR Locking Femoral Impactor , Part # 800-05-035, packaged in instrument tray FA EMP PAT TOOL KIT Part # 800-99-096
Medical Devices·410 affected·Feb 4, 2019
High RiskFDA
Roche Diagnostics Corporation
Lactate Gen.2, Catalog Nos. 03183700190, 05171881190, 11822837190, ***added as of 5/10/19*** 03183700190 Product Usage: An In vit...
Diagnostic Devices·5,292 affected·Dec 17, 2018