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. 2,624 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,624 in last 12 months

Showing 2774127760 of 51,768 recalls

Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: T10-NT Recalled by Philips Electronics North America Corporation Due to...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Panorama 1.0T Recalled by Philips Electronics North America Corporation Due...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Healthcare Lunar: a) DPX NT Recalled by GE Medical Systems Ultrasound &...

The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Multiva systems Recalled by Philips Electronics North America Corporation...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Ingenia 1.5T CX Recalled by Philips Electronics North America Corporation...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Healthcare Lunar: a) DPX Duo Recalled by GE Medical Systems Ultrasound &...

The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Intera 1.0T Recalled by Philips Electronics North America Corporation Due to...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns TCM Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Update to cooler-heater cleaning instructions.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo HX2 Temperature Management System Recalled by Terumo Cardiovascular...

The Issue: Update to cooler-heater cleaning instructions.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Intera 1.5T Recalled by Philips Electronics North America Corporation Due to...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: T5 Model 78104 Product Usage: Indicated for use as a Recalled by Philips...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Healthcare: a) Prodigy Recalled by GE Medical Systems Ultrasound &...

The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...

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

Class II — Potential Health HazardOngoing
DrugMarch 15, 2018· Bayer HealthCare Pharmaceuticals, Inc.

Recalled Item: All Alka-Seltzer Plus¿ packages with a full front panel instant Recalled by...

The Issue: Labeling: Label Mix-Up: Bayer is recalling all Alka-Seltzer Plus packages,...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 15, 2018· InvaGen Pharmaceuticals, Inc.

Recalled Item: buPROPion HCl Extended-Release Tablets Recalled by InvaGen Pharmaceuticals,...

The Issue: Failed Dissolution Specifications; during stability testing

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

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2018· InvaGen Pharmaceuticals, Inc.

Recalled Item: buPROPion HCl Extended-Release Tablets Recalled by InvaGen Pharmaceuticals,...

The Issue: Failed Dissolution Specifications; during stability testing

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 15, 2018· Biocare Medical, LLC

Recalled Item: URO-3 Triple Stain (CD44 + p53) with CK20 Recalled by Biocare Medical, LLC...

The Issue: Immunohistochemistry device kits found to display incorrect staining pattern...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2018· Teleflex Medical Europe Ltd

Recalled Item: Latex Rebreathing Bags: Product Code Equivalent Code (a) 151174050 151174...

The Issue: These products contain latex, but the following statement is not included on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2018· Teleflex Medical Europe Ltd

Recalled Item: Simplastic Suprapubic Puncture Instruments: Product Code Equivalent Code (a)...

The Issue: These products contain latex, but the following statement is not included on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2018· Teleflex Medical Europe Ltd

Recalled Item: Rectal Catheters Recalled by Teleflex Medical Europe Ltd Due to These...

The Issue: These products contain latex, but the following statement is not included on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2018· Teleflex Medical Europe Ltd

Recalled Item: Baker Jejunostomy Tubes: Product Code Equivalent Code (a) 655300160 655316...

The Issue: These products contain latex, but the following statement is not included on...

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

Class II — Potential Health HazardOngoing