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 3274132760 of 51,768 recalls

DrugDecember 28, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Flucanozole Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed Dissolution Specifications; 18 month stability time point

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 28, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Flucanozole Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed Dissolution Specifications; 18 month stability time point

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 28, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Flucanozole Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed Dissolution Specifications; 18 month stability time point

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 28, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Flucanozole Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed Dissolution Specifications; 18 month stability time point

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 28, 2016· L. Perrigo Company

Recalled Item: Clindamycin Phosphate and Benzoyl Peroxide Gel Recalled by L. Perrigo...

The Issue: Microbial Contamination of Non-Sterile Product; small number of tubes may...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 28, 2016· The Two Little Guys Company

Recalled Item: Joe Chips Retro Potato Chips Sour Cream & Toasted Onion Recalled by The Two...

The Issue: Joe Chips Sour Cream & Toasted Onion Retro Potato Chips contains a seasoning...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 27, 2016· Roland Foods, LLC.

Recalled Item: Roland MANZANILLA OLIVES STUFFED WITH ANCHOVIES Recalled by Roland Foods,...

The Issue: Product quality issue. Through sampling, FDA revealed the presence of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 27, 2016· The Harvard Drug Group

Recalled Item: Aripiprazole Tablets Recalled by The Harvard Drug Group Due to Superpotent...

The Issue: Superpotent Drug; out of specification results for assay (manufacturer)

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 27, 2016· Villa Sistemi Medicali S.P.A.

Recalled Item: Apollo Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell from...

The Issue: Patient fell from the table because the footrest of the device detached from...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2016· Villa Sistemi Medicali S.P.A.

Recalled Item: Apollo DRF Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell...

The Issue: Patient fell from the table because the footrest of the device detached from...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2016· Villa Sistemi Medicali S.P.A.

Recalled Item: Apollo EZ Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell from...

The Issue: Patient fell from the table because the footrest of the device detached from...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2016· Philips Electronics North America Corporation

Recalled Item: Philips Cisco 3850 layer 3 switch Recalled by Philips Electronics North...

The Issue: May experience a loss of centralized monitoring.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2016· Roche Diagnostics Corporation

Recalled Item: cobas p 612 pre-analytical system Recalled by Roche Diagnostics Corporation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2016· Immuno-Mycologics, Inc

Recalled Item: Cryptococcal Antigen Lateral Flow Assay (CrAg LFA) Recalled by...

The Issue: The affected products have approximately a 91% specificity while the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2016· Villa Sistemi Medicali S.P.A.

Recalled Item: Juno DRF Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell from...

The Issue: Patient fell from the table because the footrest of the device detached from...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2016· Endologix

Recalled Item: AFX Endovascular AAA System Recalled by Endologix Due to Endologix updated...

The Issue: Endologix updated the Instructions for Use (IFU) and implemented...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2016· Endologix

Recalled Item: AFX Endovascular AAA System Recalled by Endologix Due to Endologix updated...

The Issue: Endologix updated the Instructions for Use (IFU) and implemented...

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 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 Oasis Dry Suction Water Seal 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