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. 1,965 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,965 in last 12 months

Showing 1950119520 of 29,208 recalls

Medical DeviceDecember 14, 2016· Organ Recovery Systems, Inc.

Recalled Item: SPS-1 Recalled by Organ Recovery Systems, Inc. Due to Organ preservation...

The Issue: Organ preservation fluid recalled due to potential for bacterial contamination.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2016· MEDLINE INDUSTRIES INC

Recalled Item: 14 mm Distraction Pin Recalled by MEDLINE INDUSTRIES INC Due to Product's...

The Issue: Product's non-conformity involves the integrity of the seal in the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2016· Ultradent Products, Inc.

Recalled Item: NanoTips 30g 20pk Recalled by Ultradent Products, Inc. Due to Ultradent...

The Issue: Ultradent Products, Inc. announces a voluntary field action for the NanoTips...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2016· MEDLINE INDUSTRIES INC

Recalled Item: 12 mm Distraction Pin Recalled by MEDLINE INDUSTRIES INC Due to Product's...

The Issue: Product's non-conformity involves the integrity of the seal in the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT-X w/TrueV Upgrade Recalled by Siemens Medical Solutions USA...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT S(40)-4R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT Flow Edge-4R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT S(40)-3R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· On-X Life Technologies, Inc.

Recalled Item: Chord-X Chordal Sizer is designed to assist in determining the Recalled by...

The Issue: Four issues were uncovered by the recalling firm's CAPA: 1) Burrs were found...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT Flow 40-4R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT S(64)-4R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT 20 Excel Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT X-3R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· US Endoscopy Group Inc

Recalled Item: Roth Net Polyp Retrieval Recalled by US Endoscopy Group Inc Due to The firm...

The Issue: The firm was notified that the expiration date on the outer carton is...

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

Class III — Low RiskOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT S(64)-3R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Ion Beam Applications S.A.

Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to Software issue

The Issue: Software issue

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Bio mCT-S(40) 3R->4R Upgrade Recalled by Siemens Medical Solutions USA Inc....

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT X-4R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· Olympus Corporation of the Americas

Recalled Item: Uretero-reno videoscope URF-V2 and URF-V2R endoscope and accessories The...

The Issue: Olympus has received complaints regarding the breakage of the endoscope's...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2016· Great Basin Scientific, Inc.

Recalled Item: Great Basin Staph lD/R Blood Culture Panel The Great Basin Recalled by Great...

The Issue: The Great Basin Staph ID/R Panel is being recalled because the S. aureus...

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

Class II — Potential Health HazardOngoing