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. 2,572 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,572 in last 12 months

Showing 3998140000 of 51,768 recalls

Medical DeviceMay 5, 2015· Edwards Lifesciences, LLC

Recalled Item: Swan-Ganz CCO/Sv02/CEDV/VIP Thermodilution Catheters model number 744HF75....

The Issue: The product failed to meet the internal established statistical test...

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

Class II — Potential Health HazardOngoing
DrugMay 4, 2015· Ohm Laboratories, Inc.

Recalled Item: Loratadine Orally Disintegrating Tablets USP Recalled by Ohm Laboratories,...

The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.

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

Class III — Low RiskOngoing
Refund
FoodMay 4, 2015· Natural Creations Inc

Recalled Item: Natural Creations Glucosamine MSM 90 capsules packaged in 250 cc Recalled by...

The Issue: Natural Creations is recalling Glucosamine MSM dietary supplement due to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 4, 2015· Spine Wave, Inc.

Recalled Item: Spine Wave Access Kit Recalled by Spine Wave, Inc. Due to Mislabeling

The Issue: Mislabeled outer carton: Monopolar Probe is listed as 200 x 1.5mm when it...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Navigation System II-Cart Recalled by Stryker Instruments Div. of Stryker...

The Issue: Stryker initiated a device recall of the Navigation System II-Cart, Camera...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2015· Remel Inc

Recalled Item: Remel Blood Agar (TSA w/sheep blood) plate packaged Recalled by Remel Inc...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2015· Synovis Surgical Innovations, Inc.

Recalled Item: Synovis VASCU-GUARD Peripheral Vascular Patch in the following sizes and...

The Issue: Baxter healthcare is recalling specific product codes of Vascu-Guard...

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

Class I — Serious Health HazardOngoing
FoodMay 1, 2015· Poco Dolce Confections, Inc.

Recalled Item: Poco Dolce Bittersweet Chocolate: Ginger Tile Recalled by Poco Dolce...

The Issue: California Department of Public Health conducted and inspection of the firm...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 1, 2015· Poco Dolce Confections, Inc.

Recalled Item: Poco Dolce Bittersweet Chocolate: Sesame Toffee Tile Recalled by Poco Dolce...

The Issue: California Department of Public Health conducted and inspection of the firm...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 1, 2015· Poco Dolce Confections, Inc.

Recalled Item: Poco Dolce Bittersweet Chocolate: Burnt Caramel Tile Recalled by Poco Dolce...

The Issue: California Department of Public Health conducted and inspection of the firm...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 1, 2015· Poco Dolce Confections, Inc.

Recalled Item: Poco Dolce Bittersweet Chocolate: Almond Tile Recalled by Poco Dolce...

The Issue: California Department of Public Health conducted and inspection of the firm...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 1, 2015· Poco Dolce Confections, Inc.

Recalled Item: Poco Dolce Bittersweet Chocolate: Aztec Chili Tile Recalled by Poco Dolce...

The Issue: California Department of Public Health conducted and inspection of the firm...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 1, 2015· Poco Dolce Confections, Inc.

Recalled Item: Poco Dolce Bittersweet Chocolate: Almond Coconut Tile Recalled by Poco Dolce...

The Issue: California Department of Public Health conducted and inspection of the firm...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 1, 2015· Ferno-Washington Inc

Recalled Item: Wheel caster set screw for Ferno iNX Wheeled Stretcher. Ferno Recalled by...

The Issue: The firm discovered an improperly installed set screw in one caster arm...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2015· Integra LifeSciences Corp. d.b.a. Integra Pain Management

Recalled Item: Integra¿ Long Epidural Steroid Injection Needle (Tuohy Needle) Recalled by...

The Issue: Integra LifeSciences Corp. d.b.a. Integra Pain Management Announces...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2015· Beaver-Visitec International Inc.

Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...

The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2015· Beaver-Visitec International Inc.

Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...

The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2015· Beaver-Visitec International Inc.

Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...

The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2015· Beaver-Visitec International Inc.

Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...

The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2015· Beaver-Visitec International Inc.

Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...

The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...

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

Class II — Potential Health HazardOngoing