Product Recalls in Washington

Product recalls affecting Washington — including food, drugs, consumer products, medical devices, and vehicles distributed to Washington. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,612 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,612 in last 12 months

Showing 3330133320 of 51,768 recalls

FoodNovember 2, 2016· McConnell's Ice Cream, Inc.

Recalled Item: McConnell's Fine Ice Cream Turkish Coffee Recalled by McConnell's Ice Cream,...

The Issue: Potential Listeria monocytogenes contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 2, 2016· McConnell's Ice Cream, Inc.

Recalled Item: McConnell's Fine Ice Cream Vanilla Bean Recalled by McConnell's Ice Cream,...

The Issue: Potential Listeria monocytogenes contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 2, 2016· McConnell's Ice Cream, Inc.

Recalled Item: McConnell's Fine Ice Cream Salted Caramel Chip Recalled by McConnell's Ice...

The Issue: Potential Listeria monocytogenes contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 2, 2016· McConnell's Ice Cream, Inc.

Recalled Item: McConnell's Fine Ice Cream Mint Chip Recalled by McConnell's Ice Cream, Inc....

The Issue: Potential Listeria monocytogenes contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 1, 2016· CareFusion 303, Inc.

Recalled Item: Alaris System PC unit Recalled by CareFusion 303, Inc. Due to Reports where...

The Issue: Reports where the Low Battery alarm and/or the Very Low Battery alarm are...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2016· Synthes (USA) Products LLC

Recalled Item: Synthes 0.76 mm Drill Bit/Stryker J-Latch/with 5mm Stop/44.5 mm Non-Sterile...

The Issue: Package may be incorrectly labeled as containing 0.76 mm Drill Bit, but in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The possibility exists that the semi-automatic focus switch may not work as...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The possibility exists that the semi-automatic focus switch may not work as...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The possibility exists that the semi-automatic focus switch may not work as...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugNovember 1, 2016· Teva Pharmaceuticals USA

Recalled Item: Qnasl (beclomethasone dipropionate) Nasal Aerosol 40 Mcg Recalled by Teva...

The Issue: Failed Content Uniformity: Product was out of specification for spray...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugNovember 1, 2016· Teva Pharmaceuticals USA

Recalled Item: Qnasl (beclomethasone dipropionate) Nasal Aerosol 80 Mcg Recalled by Teva...

The Issue: Failed Content Uniformity: Product was out of specification for spray...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugNovember 1, 2016· Hospira Inc.

Recalled Item: Fentanyl Citrate Injection Recalled by Hospira Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Complaints of broken tips on the ampules.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 31, 2016· Spectranetics Corporation

Recalled Item: Turbo Elite Atherectomy Catheter. Models: 410-152 Recalled by Spectranetics...

The Issue: Spectranetics Corporation announces a voluntary field action for the Turbo...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2016· Spectranetics Corporation

Recalled Item: Bridge Occlusion Balloon. Model: 590-001 Temporary vessel occlusion of the...

The Issue: Spectranetics Corporation announces a voluntary field action for the Turbo...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2016· Spectranetics Corporation

Recalled Item: ELCA Coronary Atherectomy Catheter. Models: 110-001 Recalled by...

The Issue: Spectranetics Corporation announces a voluntary field action for the Turbo...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2016· Synthes (USA) Products LLC

Recalled Item: Synthes Flexible Shaft Recalled by Synthes (USA) Products LLC Due to...

The Issue: Non-conforming material used.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2016· Sorin Group USA, Inc.

Recalled Item: Perceval Sutureless Aortic Heart Valve size S Recalled by Sorin Group USA,...

The Issue: Sorin Group USA, Inc. announces a voluntary field action for the Perceval...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2016· Owens & Minor Distribution, Inc.

Recalled Item: Medi Choice Arm Slings ASL 2103 Small 7.5 x 12.5 Inch 1/EA Recalled by Owens...

The Issue: Owens & Minor is the initial importer and private label distributor of Medi...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: MSS CASSETTE GLU/LAC/UREA (BUN) as a part of the Roche Recalled by Roche...

The Issue: Incorrect Urea results may be generated sporadically on cobas b 221<6>Roche...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2016· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250 Product Usage: Proton Radiation Therapy Recalled by Mevion...

The Issue: Completing Setup Without Program Move Complete Can Cause An Isocenter Error

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing