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. 2,572 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,572 in last 12 months

Showing 4080140820 of 51,768 recalls

Medical DeviceMarch 12, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to GE Healthcare has recently...

The Issue: GE Healthcare has recently become aware of a potential safety issue due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2015· CareFusion 303, Inc.

Recalled Item: Alaris PC units Recalled by CareFusion 303, Inc. Due to CareFusion is...

The Issue: CareFusion is recalling the Alaris PC unit because of an error code. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2015· Biomet Spine, LLC

Recalled Item: Polaris 4.75 TI Spinal System Recalled by Biomet Spine, LLC Due to...

The Issue: Multiaxial screws may not meet internal requirements related to fatigue...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2015· Biomet Spine, LLC

Recalled Item: Lineum HF Torque Handle Limit (Lineum) Model Number 14-525035 P_roduct...

The Issue: Biomet is recalling the Lineum HF Torque Handle Limit (Lineum) and Torque...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2015· Biomet Spine, LLC

Recalled Item: Torque Limiting Handle (Aspen/ Alpine) Model Number 6200-1109 Product Usage:...

The Issue: Biomet is recalling the Lineum HF Torque Handle Limit (Lineum) and Torque...

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

Class II — Potential Health HazardOngoing
DrugMarch 12, 2015· Wockhardt Usa Inc.

Recalled Item: Captopril Tablets Recalled by Wockhardt Usa Inc. Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: out of specification for thickness.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 12, 2015· Trader Joes Company

Recalled Item: Cinnamon Almonds Recalled by Trader Joes Company Due to Undeclared Peanuts

The Issue: Trader Joes Company is recalling its 16 ounce packages of Trader Joes...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 12, 2015· Badia Spices, Inc.

Recalled Item: BADIA Ground Cumin Recalled by Badia Spices, Inc. Due to Undeclared Peanut

The Issue: Undeclared peanut protein.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 11, 2015· Toshiba American Medical Systems Inc

Recalled Item: INFX-8000V Interventional Angiography System. CAT-880B catheterization...

The Issue: The table base rotational brake that holds the table top may not always be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Nuclear gamma cameras (ADAC VERTEX PLUS/SOLUS/CARDIO Recalled by Philips...

The Issue: The firm was notified by a customer that the collimator exchange carriage...

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

Class II — Potential Health HazardOngoing
DrugMarch 11, 2015· Mylan Pharmaceuticals Inc.

Recalled Item: Fexofenadine HCl Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugMarch 11, 2015· Hospira Inc.

Recalled Item: LACTATED RINGER'S IRRIGATION Recalled by Hospira Inc. Due to Non-Sterility:...

The Issue: Non-Sterility: Confirmed customer report of dark, fibrous particulates...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 10, 2015· Ultra ZX Supplements

Recalled Item: ULTRA ZX DIETARY SUPPLEMENT (Extracto de Naranjo Amargo 70 Recalled by Ultra...

The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis confirmed...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 10, 2015· Mutual Pharmaceutical Company, Inc.

Recalled Item: Ergoloid Mesylates Recalled by Mutual Pharmaceutical Company, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: during long-term stability...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2015· the Compounder

Recalled Item: BIEST TD 50/50 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3))...

The Issue: Recalled products were made using an active ingredient that was recalled by...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2015· the Compounder

Recalled Item: ESTRIOL (E3) W/V (weight/volume) PGF 0.1% (1.0MG/ML) Transdermal cream...

The Issue: Recalled products were made using an active ingredient that was recalled by...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2015· the Compounder

Recalled Item: BIEST TD 83/17 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)...

The Issue: Recalled products were made using an active ingredient that was recalled by...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2015· the Compounder

Recalled Item: BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)...

The Issue: Recalled products were made using an active ingredient that was recalled by...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2015· the Compounder

Recalled Item: BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)...

The Issue: Recalled products were made using an active ingredient that was recalled by...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2015· the Compounder

Recalled Item: BIEST TD 80/20 (Estradiol (E2) Trit (yellow) / Estriol USP Recalled by the...

The Issue: Recalled products were made using an active ingredient that was recalled by...

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

Class II — Potential Health HazardOngoing
Refund