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. 1,904 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,904 in last 12 months

Showing 2740127420 of 29,208 recalls

Medical DeviceFebruary 19, 2013· Tecan US, Inc.

Recalled Item: Tecan Freedom EVO with Touch Tools Suite Version 3.0 The Recalled by Tecan...

The Issue: WIth TouchTools 3.0 after the execution of a Rich User Prompt in Display and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2013· Remel Inc

Recalled Item: Remel X/pect Flu A&B Control Swabs Recalled by Remel Inc Due to Flu A+...

The Issue: Flu A+ Control Swabs incorrectly give Flu A- results when used for quality...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 19, 2013· Trumpf Medical Systems, Inc.

Recalled Item: Helion S Exam Light or H300 The device is intended Recalled by Trumpf...

The Issue: Possible fatigue failure of the plastic joint may occur after an average use...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2013· Hospira Inc.

Recalled Item: Minibore Extension Set Recalled by Hospira Inc. Due to Hospira, Inc. is...

The Issue: Hospira, Inc. is voluntarily recalling one lot of list 14699-28, Minibore...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Ge Medical Systems Information T

Recalled Item: Centricity PACS Web Diagnostic (WebDX) by GE Healthcare Dynamic Imaging...

The Issue: It was reported from a complaint that study category labels of "Prior" and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Ge Healthcare It

Recalled Item: Imagecast PACS with Centricity RIS-IC versions prior to 10.6 Update Recalled...

The Issue: A software defect was discovered that causes images to be out of context...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· GE Healthcare

Recalled Item: The Centricity PACS Workstation is intended for use as a Recalled by GE...

The Issue: Using Merge Exam in single Study Mode may result in Missing Study Record...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Biomerieux Inc

Recalled Item: VITEK 2 XL computer system when equipped with the following Recalled by...

The Issue: There is a potential to link an isolate result to the wrong patient and then...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Biomerieux Inc

Recalled Item: VITEK 2 Compact computer system when equipped with the following Recalled by...

The Issue: There is a potential to link an isolate result to the wrong patient and then...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Biomerieux Inc

Recalled Item: VITEK 2 60 computer system when equipped with the following Recalled by...

The Issue: There is a potential to link an isolate result to the wrong patient and then...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2013· Moller Vital

Recalled Item: Molift Smart 150 Recalled by Moller Vital Due to The leg spreading mechanism...

The Issue: The leg spreading mechanism will fail to hoist and collapse if assemble...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2013· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX Micros IM2 Recalled by Horiba Instruments, Inc dba Horiba Medical Due to...

The Issue: Horiba Medical is recalling ABX Micros IM2 Data Management System because it...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 15, 2013· Moller Vital

Recalled Item: Molift Smart 150 Recalled by Moller Vital Due to The leg spreading mechanism...

The Issue: The leg spreading mechanism will fail to hoist and collapse if assemble...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2013· Becton Dickinson & Company

Recalled Item: BD Vacutainer C&S Transfer Straw Kit C&S Preservative Plus Urine Tube. 4.0...

The Issue: The BD Vacutainer Urinalysis Transfer Straw Kit #364991, Lot 1335484 has...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 14, 2013· Zimmer, Inc.

Recalled Item: Zimmer Patient Helper Bed Frame Adapter Assembly The bed frame Recalled by...

The Issue: The bed frame adapter assemblies may have a weak weld where the patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Intellispace Portal (ISP) Philips Medical Systems (Cleveland) Recalled by...

The Issue: Philips was notified of a problem using the IntelliSpace Portal with...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Oculus Innovative Sciences Inc

Recalled Item: Atrapro Antipruritic Hydrogel Recalled by Oculus Innovative Sciences Inc Due...

The Issue: Out of specification result - stability test failure of free available...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Beckman Coulter Inc.

Recalled Item: UniCel DxC 600i Synchron Access Clinical System Recalled by Beckman Coulter...

The Issue: Beckman Coulter is initiating a recall due to a defective newly released...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Polymedco, Inc

Recalled Item: Test Strips packaged in the OC-Light Manual iFOBT Kit Recalled by Polymedco,...

The Issue: The test strips in the affected product lots of the OC Light immunological...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Beckman Coulter Inc.

Recalled Item: Access 2 Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is initiating a recall due to a defective newly released...

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

Class II — Potential Health HazardOngoing