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. 1,939 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,939 in last 12 months

Showing 2230122320 of 29,208 recalls

Medical DeviceSeptember 17, 2015· Philips Electronics North America Corporation

Recalled Item: Philips DuraDiagnost stationary X-ray system Recalled by Philips Electronics...

The Issue: Buttons or keys on the monitor allow the user to turn the volume setting...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2015· LifeHealth, LLC

Recalled Item: BG cartridges for IRMA TRUPOINT Blood Gas Analyzer Recalled by LifeHealth,...

The Issue: May report values outside the published performance specifications for pH....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2015· GE Healthcare

Recalled Item: Centricity PACS IW by GE Healthcare Dynamic Imaging Solutions is Recalled by...

The Issue: Images may be missing when a system parameter MapRoute is set to a value...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2015· LifeHealth, LLC

Recalled Item: CC cartridges for IRMA TRUPOINT Blood Gas Analyzer Recalled by LifeHealth,...

The Issue: May report values outside the published performance specifications for pH....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2015· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Medical Device Identification Card for SureScan pacemaker...

The Issue: Some Medical Device Identification Cards provided to SureScan pacemaker...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Biochemical Diagnostics Inc

Recalled Item: CONSULT(TM) diagnostics hCG CONTROLS Kit Recalled by Biochemical Diagnostics...

The Issue: CONSULT diagnostics hCG Controls have discrepant storage temperatures listed...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 14, 2015· Encore Medical, Lp

Recalled Item: Turon Shoulder Impaction Fixture The Turon and RSP Recalled by Encore...

The Issue: During the Turon assembly, the impaction forces caused the polymer, black...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Smiths Medical ASD, Inc.

Recalled Item: PORT-A-CATH Plastic Hub Needles Recalled by Smiths Medical ASD, Inc. Due to...

The Issue: The label on the lid stock of the individual needle packages for a portion...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Medtronic Navigation, Inc.

Recalled Item: P/N: 9735023 Recalled by Medtronic Navigation, Inc. Due to Specific use...

The Issue: Specific use conditions can increase the possibility of a screwdriver tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Medtronic Navigation, Inc.

Recalled Item: P/N: 9734856 Recalled by Medtronic Navigation, Inc. Due to Specific use...

The Issue: Specific use conditions can increase the possibility of a screwdriver tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Encore Medical, Lp

Recalled Item: Reverse Shoulder Prosthesis Stem Impaction Fixture The Turon Recalled by...

The Issue: During the assembly, the impaction forces caused the polymer, black acetal...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· CooperSurgical, Inc.

Recalled Item: MILEX PESSARY KIT Recalled by CooperSurgical, Inc. Due to The products have...

The Issue: The products have been identified to have incorrect size prints on the MILEX...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 Computed Tomography X-ray systems. Intended to produce...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Computed Tomography X-ray systems. Intended to produce...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 16-Slice (Air) Computed Tomography X-ray systems. Intended to...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance Big Bore (Oncology & Radiology) Computed Tomography X-ray...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Flex Computed Tomography X-ray systems. Intended to produce...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 Computed Tomography X-ray systems. Intended to produce...

The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2015· Boston Scientific Corp

Recalled Item: One Step Button Recalled by Boston Scientific Corp Due to Boston Scientific...

The Issue: Boston Scientific Corp. initiated a voluntary recall of specific lots of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2015· Natus Neurology Inc

Recalled Item: NicoletOne Software v5.94 Recalled by Natus Neurology Inc Due to When using...

The Issue: When using the NicoletOne v5.94 software, after exiting the impedance check...

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

Class II — Potential Health HazardOngoing