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. 2,592 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,592 in last 12 months

Showing 3776137780 of 51,768 recalls

DrugNovember 4, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Paricalcitol Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Failed Tablet/Capsule Specifications: Product recalled due to reports of...

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

Class III — Low RiskOngoing
Refund
DrugNovember 4, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Paricalcitol Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Failed Tablet/Capsule Specifications: Product recalled due to reports of...

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

Class III — Low RiskOngoing
Refund
DrugNovember 4, 2015· Pine Pharmaceuticals, LLC

Recalled Item: Bevacizumab 1.25 mg/0.05 mL in 3/10 mL 31 G 5/16" Recalled by Pine...

The Issue: Presence of particulate matter: Presence of silicone oil microdroplets in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 4, 2015· Pine Pharmaceuticals, LLC

Recalled Item: Bevacizumab 2 mg/0.08 mL in 3/10 mL 31 G 5/16" Syringe for intravitreal...

The Issue: Presence of particulate matter: Presence of silicone oil microdroplets in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 4, 2015· Pine Pharmaceuticals, LLC

Recalled Item: Bevacizumab 2.5 mg/0.1 mL in 3/10 mL 31 G 5/16" Recalled by Pine...

The Issue: Presence of particulate matter: Presence of silicone oil microdroplets in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 4, 2015· Pine Pharmaceuticals, LLC

Recalled Item: Bevacizumab 1.25 mg/0.05 mL filled to 0.06 mL in 3/10 Recalled by Pine...

The Issue: Presence of particulate matter: Presence of silicone oil microdroplets in...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 4, 2015· Tate's Wholesale, Llc.

Recalled Item: TATE'S BAKE SHOP Cookies GINGER ZINGER GLUTEN FREE Recalled by Tate's...

The Issue: Tate's Bake Shop has recalled Chocolate Chip Cookies and Ginger Zinger...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 4, 2015· Tate's Wholesale, Llc.

Recalled Item: TATE'S BAKE SHOP CHOCOLATE CHIP COOKIES Recalled by Tate's Wholesale, Llc....

The Issue: Tate's Bake Shop has recalled Chocolate Chip Cookies and Ginger Zinger...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 4, 2015· Land O' Lakes, Inc

Recalled Item: Kozy Shack Indulgent Salted Caramel Recalled by Land O' Lakes, Inc Due to...

The Issue: Kozy Shack is recalling one lot of Kozy Shack Indulgent Recipe Pudding in a...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 4, 2015· Edwards Lifesciences, LLC

Recalled Item: Thin-Flex Venous Cannula Recalled by Edwards Lifesciences, LLC Due to...

The Issue: Edwards Lifesciences initiated a field action for the Thin-Flex Venous...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2015· Ormco/Sybronendo

Recalled Item: Copper NiTi Preformed Archwires Recalled by Ormco/Sybronendo Due to Ormco...

The Issue: Ormco Corporation is recalling Copper NiTi Preformed Archwires because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Diagnostic Hybrids, Inc.

Recalled Item: MicroVue SC5b-9 Plus EIA (CE-IVD) Recalled by Diagnostic Hybrids, Inc. Due...

The Issue: A component of the kit was found to contain bacterial contamination.

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

Class III — Low RiskOngoing
Medical DeviceNovember 3, 2015· Diagnostic Hybrids, Inc.

Recalled Item: MicroVue SC5b-9 Plus EIA (RUO) Recalled by Diagnostic Hybrids, Inc. Due to A...

The Issue: A component of the kit was found to contain bacterial contamination.

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

Class III — Low RiskOngoing
Medical DeviceNovember 3, 2015· Diagnostic Hybrids, Inc.

Recalled Item: MicroVue CIC-C1q EIA Recalled by Diagnostic Hybrids, Inc. Due to A component...

The Issue: A component of the kit was found to contain bacterial contamination.

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

Class III — Low RiskOngoing
Medical DeviceNovember 3, 2015· AngioDynamics Inc.

Recalled Item: NAMIC CONVENIENCE KIT SELF REGIONAL HEALTHCARE PV LEG PACK Recalled by...

The Issue: Procedure Products initiated the recall due to the inner lumen of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· AngioDynamics Inc.

Recalled Item: NAMIC CONVENIENCE KIT MERCY GENERAL HOSPITAL NEURO KIT Recalled by...

The Issue: Procedure Products initiated the recall due to the inner lumen of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· AngioDynamics Inc.

Recalled Item: NAMIC CONVENIENCE KIT HOLYOKE HOSPITAL SPECIAL PROCEDURE KIT Recalled by...

The Issue: Procedure Products initiated the recall due to the inner lumen of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· AngioDynamics Inc.

Recalled Item: NAMIC CONVENIENCE KIT RENOWN REGIONAL MEDICAL CENTER Recalled by...

The Issue: Procedure Products initiated the recall due to the inner lumen of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD10 Recalled by Philips Electronics North America Corporation...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: INTEGRIS V3000 Recalled by Philips Electronics North America Corporation Due...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing