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. 1,788 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,788 in last 12 months

Showing 4188141900 of 51,768 recalls

DrugDecember 5, 2014· Eisai Inc

Recalled Item: BELVIQ¿ (Lorcaserin HCl) Tablets Recalled by Eisai Inc Due to...

The Issue: Labeling:Missing Label: Bottles may not have a product label, or have a...

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

Class III — Low RiskOngoing
Refund
FoodDecember 5, 2014· Safeway Inc

Recalled Item: Safeway Select French Salted Caramel (Fleur De Sel) Premium Ice Cream...

The Issue: The recipe's caramel cups ingredient was replaced with peanut butter cups...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 4, 2014· Abdallah Candies, Inc

Recalled Item: Abdallah Milk Chocolate Bites CARAMEL Recalled by Abdallah Candies, Inc Due...

The Issue: Abdallah Candies is recalling red and silver foil wrapped Holiday Caramel...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 4, 2014· Micro Labs Usa, Inc S

Recalled Item: Simvastatin Tablets Recalled by Micro Labs Usa, Inc S Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Product failed a known...

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

Class III — Low RiskOngoing
Refund
DrugDecember 4, 2014· Micro Labs Usa, Inc S

Recalled Item: Simvastatin Tablets Recalled by Micro Labs Usa, Inc S Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Product failed a known...

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

Class III — Low RiskOngoing
Refund
DrugDecember 4, 2014· K C Pharmaceuticals Inc

Recalled Item: Eye Drops Industrial Strength (Polyethylene glycol 400 1% Recalled by K C...

The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...

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

Class III — Low RiskOngoing
Refund
DrugDecember 4, 2014· K C Pharmaceuticals Inc

Recalled Item: Eye Drops A.C. (Tetrahydrozoline HCl 0.05% Recalled by K C Pharmaceuticals...

The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...

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

Class III — Low RiskOngoing
Refund
DrugDecember 4, 2014· Baxter Healthcare Corp

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corp Due to...

The Issue: Presence of Particulate Matter: Confirmed customer complaints received for...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 4, 2014· K C Pharmaceuticals Inc

Recalled Item: Eye Drops (Tetrahydrozoline HCl 0.05%) Recalled by K C Pharmaceuticals Inc...

The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...

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

Class III — Low RiskOngoing
Refund
DrugDecember 4, 2014· K C Pharmaceuticals Inc

Recalled Item: Eye Drops Advanced Relief (Dextran 70 0.1% Recalled by K C Pharmaceuticals...

The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...

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

Class III — Low RiskOngoing
Refund
DrugDecember 4, 2014· Micro Labs Usa, Inc S

Recalled Item: Simvastatin Tablets Recalled by Micro Labs Usa, Inc S Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Product failed a known...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 4, 2014· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Imbibe Aliquot Needle Bone Cement Needle- Model...

The Issue: There is the potential for a breach in the inner or outer packaging pouches...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2014· Hansen Medical Inc

Recalled Item: Sensei X Robotic Catheter System Recalled by Hansen Medical Inc Due to The...

The Issue: The Set Up Joint subassembly of the Sensei X Robotic Catheter System may...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2014· Zimmer Manufacturing B.V.

Recalled Item: Trilogy¿ Fiber Metal Acetabular Shell Size 54 mm OD The Recalled by Zimmer...

The Issue: Zimmer received a single complaint wherein a Trilogy® Fiber Metal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2014· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Imbibe Bone Marrow Aspiration Needle Recalled by...

The Issue: There is the potential for a breach in the inner or outer packaging pouches...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2014· Musculoskeletal Transplant Foundation, Inc.

Recalled Item: DBX Mix Recalled by Musculoskeletal Transplant Foundation, Inc. Due to The...

The Issue: The seal on the DBX Mix outer PETG/Aclar tray with foil lid packaging for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Arjo Hospital Equipment AB

Recalled Item: Rotoprone Therapy System. The Rotoprone Therapy System is an advanced...

The Issue: The recalled devices labeling and instructions for use contain unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Arjo Hospital Equipment AB

Recalled Item: RotoRest Delta Advanced Therapy System. The RotoRest Delta Advanced Kinetic...

The Issue: The recalled devices labeling and instructions for use contain unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Arjo Hospital Equipment AB

Recalled Item: TriaDyne Proventa Critical Care Therapy System. The TriaDyne Proventa...

The Issue: The recalled devices labeling and instructions for use contain unapproved...

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

Class II — Potential Health HazardOngoing
DrugDecember 3, 2014· Hospira Inc.

Recalled Item: MitoXANTRONE Injection Recalled by Hospira Inc. Due to Failed Stability...

The Issue: Failed Stability Specifications: Product is subpotent and has out of...

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

Class I — Serious Health HazardOngoing
Refund