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. 2,432 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,432 in last 12 months

Showing 5024150260 of 51,768 recalls

Medical DeviceAugust 2, 2012· Kreg Medical Inc.

Recalled Item: E-Z WIDER BARIATRIC CHAIR BED Recalled by Kreg Medical Inc. Due to An EZ...

The Issue: An EZ Wider bed (capacity of 1000 lb. safe working load collapsed during...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2012· Hospira, Inc.

Recalled Item: Sterile Empty Vial and Injector (30mL PCA vial) Recalled by Hospira, Inc....

The Issue: Reports of leaking during filling and administration.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2012· Steris Corporation

Recalled Item: 100 ft roll of tubing inside a cardboard box. Medical Recalled by Steris...

The Issue: On 7/20/2012 the firm became aware that a lot of tubing was distributed by...

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

Class III — Low RiskOngoing
Medical DeviceAugust 2, 2012· Phadia US Inc

Recalled Item: PHADIA Varelisa Cardiolipin IgM Cardiolipin autoantibody immunological test...

The Issue: Customers were not following the labeled assay procedure. This was due to a...

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

Class III — Low RiskOngoing
DrugAugust 1, 2012· Dr. Reddy's Laboratories, Inc.

Recalled Item: Citalopram tablets USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Chemical Contamination: The product is being recalled due to complaints...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 1, 2012· Dr. Reddy's Laboratories, Inc.

Recalled Item: Citalopram tablets USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Chemical Contamination: The product is being recalled due to complaints...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 1, 2012· Dr. Reddy's Laboratories, Inc.

Recalled Item: Citalopram tablets USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Chemical Contamination: The product is being recalled due to complaints...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 1, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima XR 220amx 30kw Mobile X-ray System The Recalled by GE...

The Issue: GE Healthcare has become aware of a software issue on the interface of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima XR 200 amx with Digital Upgrade. The Recalled by GE...

The Issue: GE Healthcare has become aware of a software issue on the interface of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima XR 220amx 15kw Mobile X-Ray System The Recalled by GE...

The Issue: GE Healthcare has become aware of a software issue on the interface of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2012· Steris Corporation

Recalled Item: The SYSTEM 1E Liquid Sterilant Processing System. The SYSTEM 1E Recalled by...

The Issue: The firm initiated a recall after complaint investigations revealed that...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2012· Nellcor Puritan Bennett Inc. (dba Covidien LP)

Recalled Item: DGPHP RFA High-Power Single Use Grounding Pads and Cool-Tip RFA Recalled by...

The Issue: Covidien is conducting a recall of various production lots of DGHP RFA High...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2012· Respironics California Inc

Recalled Item: V60 Ventilator Recalled by Respironics California Inc Due to Respironics is...

The Issue: Respironics is recalling the V60 ventilator because certain blower motor...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2012· DePuy Orthopaedics, Inc.

Recalled Item: DePuy Custom Implant Devices Packaging: Packaging was not standardized on...

The Issue: In connection with a Warning Letter received from the U.S. Food & Drug...

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

Class II — Potential Health HazardOngoing
DrugJuly 30, 2012· Genentech Inc

Recalled Item: Trastuzumab Kit containing 1 vial Trastuzumab (nominal content: 440 mg)...

The Issue: Presence of Particulate Matter: One lot of Bacteriostatic Water for...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 30, 2012· Mallinckrodt Inc

Recalled Item: Thallous Chloride Tl 201 Injection Recalled by Mallinckrodt Inc Due to...

The Issue: Labeling: Correct Labeled Product Miscart/Mispack: labels on outer...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 30, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Emit(R) 2000 Phenobarbital Assay (OSR4D229) and Syva(R) Emit(R)...

The Issue: Firm has confirmed highter imprecision with the recalled lots on Beckman...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2012· Imaging Sciences International, LLC

Recalled Item: DEXIS Imaging Suite - catalog number 1.008.7932 Recalled by Imaging Sciences...

The Issue: A condition can occur during renumbering of the patient database using the...

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

Class II — Potential Health HazardOngoing
DrugJuly 27, 2012· Natural Essentials Inc

Recalled Item: Oasis Age Essential (cetylpyridinium chloride) Mouthwash Recalled by Natural...

The Issue: Microbial Contamination of a Non-Sterile Products: Three product lots are...

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

Class III — Low RiskOngoing
Refund
DrugJuly 27, 2012· Capco Custom Packaging Inc

Recalled Item: Eco-Dent Sparkling Clean Mint Ultimate Essential MouthCare Recalled by Capco...

The Issue: Microbial Contamination of Non-Sterile Products; Product was found to be...

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

Class II — Potential Health HazardOngoing
Refund