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. 954 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
954 in last 12 months

Showing 48681–48700 of 51,768 recalls

DrugFebruary 27, 2013· Mutual Pharmaceutical Company, Inc.

Recalled Item: Fenofibric Acid Recalled by Mutual Pharmaceutical Company, Inc. Due to...

The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 27, 2013· Mutual Pharmaceutical Company, Inc.

Recalled Item: FIBRICOR (fenofibric acid) Tablets Recalled by Mutual Pharmaceutical...

The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 27, 2013· Mutual Pharmaceutical Company, Inc.

Recalled Item: Fenofibric Acid Recalled by Mutual Pharmaceutical Company, Inc. Due to...

The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 27, 2013· Hospira Inc.

Recalled Item: The LifeCare PCA infusion system with Hospira MedNet software allows...

The Issue: The infusion pump has a clear plastic door that, due to its design, allows...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2013· Hospira Inc.

Recalled Item: The PCA 3 infusion pump allows clinicians Recalled by Hospira Inc. Due to...

The Issue: The infusion pump has a clear plastic door that, due to its design, allows...

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

Class II — Potential Health HazardOngoing
FoodFebruary 27, 2013· Koda Farms Inc

Recalled Item: Mochiko Blue Star Sweet Rice Flour Recalled by Koda Farms Inc Due to Koda...

The Issue: Koda Farms received a report from a customer that a hard yellow material was...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 26, 2013· Kroger Co

Recalled Item: Tender Twist Wheat Bread NET WT 20 OZ (1 LB Recalled by Kroger Co Due to The...

The Issue: The firm was notified of bread with traces of visible ink was discovered...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 26, 2013· Kroger Co

Recalled Item: Tender Twist 100% Whole Wheat Bread 24 oz (1 LB Recalled by Kroger Co Due to...

The Issue: The firm was notified of bread with traces of visible ink was discovered...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 26, 2013· Kroger Co

Recalled Item: Fred Meyer Tender Twist Honey Cracked Wheat Bread 24 oz Recalled by Kroger...

The Issue: The firm was notified of bread with traces of visible ink was discovered...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 26, 2013· Kroger Co

Recalled Item: Kroger Value Wheat Bread Recalled by Kroger Co Due to The firm was notified...

The Issue: The firm was notified of bread with traces of visible ink was discovered...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 26, 2013· Hospira Inc.

Recalled Item: Diazepam Injection Recalled by Hospira Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 26, 2013· Hospira Inc.

Recalled Item: Furosemide Injection Recalled by Hospira Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 26, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Cefdinir for Oral Suspension Recalled by Teva Pharmaceuticals USA, Inc. Due...

The Issue: Defective Container: This recall is being carried out due to the potential...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 26, 2013· Hospira Inc.

Recalled Item: Sodium Acetate Injection Recalled by Hospira Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 26, 2013· Mylan Pharmaceuticals Inc.

Recalled Item: Lisinopril Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Tablets/Capsules Imprinted With Wrong ID: Pharmaceuticals are imprinted with...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 26, 2013· Hospira Inc.

Recalled Item: QUELICIN (succinylcholine chloride) Injection Recalled by Hospira Inc. Due...

The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: Cooper Surgical Gellhorn Flexible Pessary 3" Recalled by Cooper Surgical,...

The Issue: Pessary mislabeled outer package may not the size of the product contained...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: Cooper Surgical Incontinence Dish w/ Support Pessary #0 Recalled by Cooper...

The Issue: Pessary mislabeled outer package may not the size of the product contained...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2013· Hill-Rom, Inc.

Recalled Item: TotalCare SpO2RT2 bed. Product Usage: Bed Recalled by Hill-Rom, Inc. Due to...

The Issue: In certain situations a software problem with the TotalCare SpO2RT¿ 2 bed...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: Cooper Surgical Incontinence Ring Flexible Pessary #4 Recalled by Cooper...

The Issue: Pessary mislabeled outer package may not the size of the product contained...

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

Class III — Low RiskOngoing