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. 2,624 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,624 in last 12 months

Showing 2758127600 of 51,768 recalls

DrugApril 5, 2018· Coastal Meds, LLC.

Recalled Item: LIPO-DEN PLUS Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr....

The Issue: Presence of Particulate matter. Recall due to presence of unknown...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2018· Coastal Meds, LLC.

Recalled Item: LIPO-B Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr. Recalled...

The Issue: Presence of Particulate matter. Recall due to presence of unknown...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 5, 2018· Abbott

Recalled Item: Thoratec HeartMate 3 LVAS Implant Kit Recalled by Abbott Due to Reports of...

The Issue: Reports of outflow graft twist occlusions. Patients whose devices experience...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 4, 2018· Handpiece Headquarters

Recalled Item: Henry Schein CU 1000 Halogen Curing Light Recalled by Handpiece Headquarters...

The Issue: Tip of the curing light was too hot causing a heat sensation in the patients.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2018· Deerfield Imaging, Inc.

Recalled Item: IMRIS IMRI 1.5T AND 3T S System Product Usage: The Recalled by Deerfield...

The Issue: The DC power to the IFOSS collision detector control panel at your facility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2018· Menarini Silicon Biosystems

Recalled Item: CELLSEARCH¿ CIRCULATING Tumor Cell Kits (IVD) (Product Code 7900001)...

The Issue: Unusually high number of total images/unassigned events may require...

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

Class II — Potential Health HazardOngoing
FoodApril 4, 2018· Avalanche Distributing, LLC

Recalled Item: Scotcharoo Valanga Gourmet Recalled by Avalanche Distributing, LLC Due to...

The Issue: Scotcharoo product is recalled because the Contains statement does not...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 3, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter Sigma Spectrum Infusion Pump with master Drug Library (Version...

The Issue: Service technician improperly documented final release testing on product,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...

The Issue: Service technician improperly documented final release testing on product,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...

The Issue: Service technician improperly documented final release testing on product,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...

The Issue: Service technician improperly documented final release testing on product,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter Sigma Spectrum Infusion Pump with master Drug Library (Version...

The Issue: Service technician improperly documented final release testing on product,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2018· Synthes (USA) Products LLC

Recalled Item: Retractor f/Sciatic Nerve Recalled by Synthes (USA) Products LLC Due to...

The Issue: There is a potential for microspores to form on the hollow handle of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Modular Head Component Recalled by Zimmer Biomet, Inc. Due to Two lots of...

The Issue: Two lots of different sized modular heads potentially commingled. Risks...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Modular Head Component Recalled by Zimmer Biomet, Inc. Due to Two lots of...

The Issue: Two lots of different sized modular heads potentially commingled. Risks...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2018· Synthes (USA) Products LLC

Recalled Item: Retractor f/Sciatic Nerve Long Recalled by Synthes (USA) Products LLC Due to...

The Issue: There is a potential for microspores to form on the hollow handle of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: T2100 Micro flex Drive Treadmill Recalled by GE Medical Systems Ultrasound &...

The Issue: A performance issue with customer owned spare parts, T2100 Microflex drive...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2018· Bio-Rad Laboratories Inc

Recalled Item: PR4100 Microplate Reader US Recalled by Bio-Rad Laboratories Inc Due to The...

The Issue: The connector of the power supply was capable of fitting other components...

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

Class II — Potential Health HazardOngoing
DrugApril 2, 2018· Diamond Wipes International, Inc.

Recalled Item: ACURE Recalled by Diamond Wipes International, Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: finished products were manufactured with poor quality water.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2018· Diamond Wipes International, Inc.

Recalled Item: WipeEssentials Wet Wipes (benzalkonium chloride 0.13%) Recalled by Diamond...

The Issue: CGMP Deviations: finished products were manufactured with poor quality water.

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

Class II — Potential Health HazardOngoing
Refund