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. 2,653 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,653 in last 12 months

Showing 2462124640 of 51,768 recalls

Medical DeviceDecember 6, 2018· Vygon U.S.A.

Recalled Item: Vyon DUALSTOP White Cap used for intravascular lines Product Code: Recalled...

The Issue: DualStop Caps defect causing leaks in affected product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2018· Vygon U.S.A.

Recalled Item: Vygon DUALSTOP Red Cap used for intravascular lines Product Code: Recalled...

The Issue: DualStop Caps defect causing leaks in affected product

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

Class II — Potential Health HazardOngoing
DrugDecember 6, 2018· Pfizer Inc.

Recalled Item: Levoxyl (levothyroxine sodium tablets Recalled by Pfizer Inc. Due to...

The Issue: Superpotent Drug.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 6, 2018· Medtronic Navigation, Inc.

Recalled Item: Medtronic Adapter Percutaneous Pin Recalled by Medtronic Navigation, Inc....

The Issue: Under certain circumstances, the percutaneous pin adapter used with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2018· Carl Zeiss Meditec, Inc.

Recalled Item: VisuMax Software Version 2.10.13 with activated Software-Module ReLEx...

The Issue: VisuMax devices with software version 2.10.13 and activated SW-Module ReLEx...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2018· Sage Products Inc

Recalled Item: Toothete Oral Care Sodium Bicarbonate Mouthpaste Recalled by Sage Products...

The Issue: A voluntary recall of a lot (67924) of Independent Care System due to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2018· Medela Inc

Recalled Item: Breast Milk Transfer Lid for use with Oral Syringe Connectors Model:...

The Issue: The sterility may be compromised due to a potential breach in the packaging,...

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

Class III — Low RiskOngoing
DrugDecember 5, 2018· Pharmedium Services, LLC

Recalled Item: Fentanyl Citrate 2 mcg per mL (200 mcg per 100 Recalled by Pharmedium...

The Issue: Sub-potent

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 5, 2018· Pharmedium Services, LLC

Recalled Item: Fentanyl Citrate 2 mcg per mL (100 mcg per 50 Recalled by Pharmedium...

The Issue: Sub-potent

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 5, 2018· Beckman Coulter Inc.

Recalled Item: UniCel DxC 660i Recalled by Beckman Coulter Inc. Due to When racks are...

The Issue: When racks are front-loaded onto the sample presentation unit while samples...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2018· Beckman Coulter Inc.

Recalled Item: The UniCel DxI 600 and 800 Access Immunoassay Systems Recalled by Beckman...

The Issue: When racks are front-loaded onto the sample presentation unit while samples...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2018· Exactech, Inc.

Recalled Item: Equinoxe Preserve Humeral Stem Recalled by Exactech, Inc. Due to Possibility...

The Issue: Possibility that the Equinoxe Preserve Humeral Stem, 8mm, was inadvertently...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2018· Agfa-Gevaert, N.V.

Recalled Item: DX-D 600 DIRECT RADIOGRAPHY SYSTEM Product Usage: The DX-D 600 Recalled by...

The Issue: After an upgrade of the software of the Overhead Tube Crane, there were...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2018· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: BiMobile UHMWPE Liner: ID-28mm/OD-50mm Recalled by Waldemar Link GmbH & Co....

The Issue: The internal labeling included with these implants may include incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2018· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: BiMobile UHMWPE Liner: ID-28mm/OD-54mm Recalled by Waldemar Link GmbH & Co....

The Issue: The internal labeling included with these implants may include incorrect...

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

Class II — Potential Health HazardOngoing
DrugDecember 4, 2018· Epic Pharma, LLC

Recalled Item: Estradiol Tablets Recalled by Epic Pharma, LLC Due to Presence of foreign...

The Issue: Presence of foreign tablet/capsule: A single foreign tablet was found in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 4, 2018· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Triton Sponge System (Software) Recalled by Stryker Instruments Div. of...

The Issue: Gauss Surgical is updating the Instructions for Use (IFU) for our Triton...

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

Class III — Low RiskOngoing
FoodDecember 4, 2018· Earthworks Health

Recalled Item: Diatomaceous Earth packaged in the following ways: 1) Perma-Guard Recalled...

The Issue: Product contains elevated levels of lead, arsenic, and chromium: potentially...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 4, 2018· Bauer's Candies, Inc.

Recalled Item: Bourbon Sea Salt Bauer's Candies Caramels NET WT 4 oz & 8 oz (bag) & bulk...

The Issue: Risk of Hepatitis A exposure.

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 4, 2018· Bauer's Candies, Inc.

Recalled Item: Bauer's Candies Chocolate Modjeskas NET WT 4 oz & 8 oz bags Recalled by...

The Issue: Risk of Hepatitis A exposure.

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

Class II — Potential Health HazardOngoing
Refund