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. 2,486 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,486 in last 12 months

Showing 4186141880 of 51,768 recalls

Medical DeviceDecember 12, 2014· Biocare Medical Llc

Recalled Item: MUM-1 (Multiple myeloma oncogene-1) Recalled by Biocare Medical Llc Due to...

The Issue: Three lots of MUM-1 may not meet their labeled shelf life, as a drop in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2014· Owen Mumford USA, Inc.

Recalled Item: Autopen Classic Automatic insulin delivery pen Recalled by Owen Mumford USA,...

The Issue: The dials in the Autopens are not working - the dial does not stay dialed,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2014· Zimmer, Inc.

Recalled Item: Persona (TASP) Tibial Articular Surface Provisional Shim Recalled by Zimmer,...

The Issue: Potential for delay in surgery and/or ball bearings to be left in the wound....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2014· Mentor Texas, LP.

Recalled Item: MENTOR MemoryGel Resterilizable Gel Sizer Moderate Plus Profile STERILE....

The Issue: The IFU provided in the affected units of the MENTOR MemoryGel...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2014· Richard Wolf Medical Instruments Corp.

Recalled Item: The I-Cart is used to store Recalled by Richard Wolf Medical Instruments...

The Issue: The transformers installed on carts used for Richard Wolf medical video...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2014· Covidien

Recalled Item: Covidien Trellis-8 Peripheral Infusion System. Models CVT808015 Recalled by...

The Issue: A manufacturing error resulted in the risk of incorrect proximal and distal...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 10, 2014· Covidien

Recalled Item: Covidien Trellis-6 Peripheral Infusion System. Models BVT608010V01 Recalled...

The Issue: A manufacturing error resulted in the risk of incorrect proximal and distal...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 10, 2014· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to Potential unintentional...

The Issue: Potential unintentional system motion or rotation due to a positioning user...

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

Class II — Potential Health HazardOngoing
DrugDecember 9, 2014· Akorn, Inc.

Recalled Item: Triamcinolone Acetonide Lotion USP Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: The known impurity went out of...

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

Class III — Low RiskOngoing
Refund
DrugDecember 9, 2014· J. Strickland and Co

Recalled Item: sulfur8(R) medicated anti-dandruff conditioner Recalled by J. Strickland and...

The Issue: Failed pH specification: Product pH test value of 5.72 failed to meet its...

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

Class III — Low RiskOngoing
Refund
FoodDecember 8, 2014· Anabolic Science Labs, LLC

Recalled Item: "***SLIM X LEAN HOUR 12+ HOUR ENERGY***PRODUCT ID: ASL-SXL-03***Manufactured...

The Issue: This product is being recalled due to the presence of undeclared synthetic...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 8, 2014· Baxter Healthcare Corp.

Recalled Item: Baxter Integrated APD Set with Cassette 3-Prong Recalled by Baxter...

The Issue: Baxter is issuing a recall for one lot of Integrated Automated Peritoneal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2014· Radiometer America Inc

Recalled Item: ABL90 FLEX analyzer Recalled by Radiometer America Inc Due to The ABL90...

The Issue: The ABL90 analyzer does not always use the most recent calibration data to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2014· Mobius Imaging, LLC

Recalled Item: Airo Mobile Intraoperative CT I Airo Recalled by Mobius Imaging, LLC Due to...

The Issue: There is a risk that during the transfer of an image and navigation data to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2014· Philips Medical Systems (Cleveland) Inc

Recalled Item: Various Brilliance and Ingenuity Computed Tomography X-ray systems Recalled...

The Issue: Improper assembly of the vertical motor/brake system may lead to uncommanded...

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

Class II — Potential Health HazardOngoing
DrugDecember 5, 2014· Eisai Inc

Recalled Item: BELVIQ¿ (Lorcaserin HCl) Tablets Recalled by Eisai Inc Due to...

The Issue: Labeling:Missing Label: Bottles may not have a product label, or have a...

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

Class III — Low RiskOngoing
Refund
FoodDecember 5, 2014· Safeway Inc

Recalled Item: Safeway Select French Salted Caramel (Fleur De Sel) Premium Ice Cream...

The Issue: The recipe's caramel cups ingredient was replaced with peanut butter cups...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 5, 2014· Invacare Corporation

Recalled Item: G- Series Beds Recalled by Invacare Corporation Due to Invacare identified...

The Issue: Invacare identified that the rail mounting bracket on the G29 full length...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2014· Intuitive Surgical, Inc.

Recalled Item: IS3000 Vision Side Cart (VSC) used in conjunction with the Recalled by...

The Issue: Intuitive Surgical is initiating a voluntary correction related to da Vinci...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2014· Alere San Diego, Inc.

Recalled Item: Alere INRatio PT/INR Test Strips Recalled by Alere San Diego, Inc. Due to In...

The Issue: In certain cases, an INRatio PT/INR Monitor system may provide an INR result...

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

Class I — Serious Health HazardOngoing