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. 2,612 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,612 in last 12 months

Showing 3276132780 of 51,768 recalls

Medical DeviceDecember 23, 2016· Elekta, Inc.

Recalled Item: Oncentra External Beam Oncentra Brachy Product Usage: Oncentra is radiation...

The Issue: Cross profile for Varian 60 degree wedge shows "horns."

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView X upgraded to XCT 882454 Recalled by Philips Medical Systems...

The Issue: The intended use listed in the English and localized language IFUs for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Atrium Medical Corporation

Recalled Item: Maquet Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation...

The Issue: Chest drains manual vent valve located at the top of affected chest drains...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Atrium Medical Corporation

Recalled Item: Maquet Express Dry Seal Suction OASIS DRAIN Recalled by Atrium Medical...

The Issue: Chest drains manual vent valve located at the top of affected chest drains...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· The Binding Site Group, Ltd.

Recalled Item: Optilite IgG4 Kit Product Code: LK009.OPT.A Recalled by The Binding Site...

The Issue: A change to the lower end of the measuring range and product insert did not...

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

Class III — Low RiskOngoing
Medical DeviceDecember 23, 2016· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: CARDIOSAVE Hybrid IABP and CARDIOSAVE Rescue IABP affected part number...

The Issue: Maquet has received 3 confirmed complaints related to the Li-lon Battery...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Atrium Medical Corporation

Recalled Item: Maquet Express Dry Seal Suction OCEAN DRAIN Recalled by Atrium Medical...

The Issue: Chest drains manual vent valve located at the top of affected chest drains...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Atrium Medical Corporation

Recalled Item: Maquet Express Dry Seal Suction Chest Drain Recalled by Atrium Medical...

The Issue: Chest drains manual vent valve located at the top of affected chest drains...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: The intended use listed in the English and localized language IFUs for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2016· Tosoh Smd Inc

Recalled Item: Keyspan High-High Speed USB to Serial Adapter Product Usage: The Recalled by...

The Issue: Power outages causes reporting software to shutdown.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2016· Mako Surgical Corporation

Recalled Item: MAKO RIO THA Application User Guides Recalled by Mako Surgical Corporation...

The Issue: Five (5) AFMEA Risk Control Measures are missing from the MAKO RIO THA...

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

Class II — Potential Health HazardOngoing
DrugDecember 22, 2016· Roxane Laboratories, Inc.

Recalled Item: Furosemide Tablets USP Recalled by Roxane Laboratories, Inc. Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: An unusually thick tablet was reported...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2016· Aurobindo Pharma USA Inc

Recalled Item: Venlafaxine Hydrochloride extended release capsules Recalled by Aurobindo...

The Issue: Failed Tablet/Capsule Specifications: Some bottles contain punctured, and/or...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2016· Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals

Recalled Item: TEMAZEPAM CAPSULES USP Recalled by Vintage Pharmaceuticals LLC, DBA...

The Issue: Failed Stability Specifications

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

Class III — Low RiskOngoing
Refund
FoodDecember 22, 2016· Schreiber Food International

Recalled Item: Ambrosia Quality Foods Brand 4/1 gallon Worcestershire Sauce Net 128 Fl. Oz....

The Issue: Ambrosia brand 4/1 Gallon Worcestershire Sauce may contain undeclared peanuts.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 22, 2016· AGFA Healthcare Corp.

Recalled Item: IMPAX Cardiovascular The IMPAX CV Reporting module consists of a Recalled by...

The Issue: A customer experienced when using IMPAX CV Reporting software, specifically,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2016· AGFA Healthcare Corp.

Recalled Item: Agfa Healthcare NX 3.0.8950 Imaging Processing Software Recalled by AGFA...

The Issue: A customer reported that when using an NX workstation with software version...

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

Class II — Potential Health HazardOngoing
FoodDecember 21, 2016· Rich Products Corp

Recalled Item: Jon Donaire Ice Cream Layer Cake Recalled by Rich Products Corp Due to...

The Issue: The product may contain undeclared walnuts from intermediate layer cake...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 21, 2016· Rich Products Corp

Recalled Item: RICH'S 1/4 Sheet White Cake with Vanilla Ice Cream Cake Recalled by Rich...

The Issue: The product may contain undeclared walnuts from intermediate layer cake...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 21, 2016· Rich Products Corp

Recalled Item: Signature SELECT Vanilla Ice Cream & White Cake ICE CREAM CAKE Recalled by...

The Issue: The product may contain undeclared walnuts from intermediate layer cake...

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

Class II — Potential Health HazardOngoing
Refund