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. 2,433 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,433 in last 12 months

Showing 4898149000 of 51,768 recalls

Medical DeviceJanuary 28, 2013· Sorin Group USA, Inc.

Recalled Item: Isoline Implantable Defibrillation Lead Recalled by Sorin Group USA, Inc....

The Issue: Isoline defibrillation leads distributed may have internal insulation breach.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2013· Philips Healthcare Inc.

Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290 The...

The Issue: Philips HeartStart XL+ Defibrillator/Monitor may become locked out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2013· ConMed Corporation

Recalled Item: ELECTROLASE(R) HYFRECATOR(R) ELECTRODES - BLUNT Recalled by ConMed...

The Issue: Some devices had broken through the seal of the sterile pouch. ConMed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2013· ConMed Corporation

Recalled Item: ELECTROLASE HYFRECATOR(R) ELECTRODES - SHARP Recalled by ConMed Corporation...

The Issue: Some devices had broken through the seal of the sterile pouch. ConMed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2013· Varian Medical Systems, Inc. Oncology Systems

Recalled Item: Varian Eclipse Treatment Planning System for Radiotherapy Recalled by Varian...

The Issue: The calculation of dose dynamic plans containing different energy fields is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2013· Prism Medical Services USA

Recalled Item: Prism Medical C-Series Carry Bar Recalled by Prism Medical Services USA Due...

The Issue: The firm replaced the recalled carry bar with a plastic insert with a carry...

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

Class II — Potential Health HazardOngoing
DrugJanuary 25, 2013· Hospira Inc.

Recalled Item: Lactated Ringer's and 5% Dextrose Injection Recalled by Hospira Inc. Due to...

The Issue: Non-Sterility: Confirmed customer complaint of product contaminated with mold.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 25, 2013· Mandalay Trading Corporation

Recalled Item: Tausi Brand Salted Black Beans Recalled by Mandalay Trading Corporation Due...

The Issue: Mandalay Trading is recalling Tausi Brand Salted Black Beans because it may...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 25, 2013· Mc-NEIL-PPC, Inc.

Recalled Item: KY SENSITIVE TM JELLY Personal Lubricant. The product is packaged Recalled...

The Issue: This product is not cleared for marketing in the US.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2013· Nellcor Puritan Bennett Inc. (dba Covidien LP)

Recalled Item: Puritan Bennett 700 Series Ventilators (PB740 and PB760) PB700 Series...

The Issue: Covidien is correcting labeling to clarify the operational life of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2013· Nellcor Puritan Bennett Inc. (dba Covidien LP)

Recalled Item: Puritan Bennett 840 Series Ventilator PB840 Operators Manual Addendum PN...

The Issue: Covidien is correcting labeling to clarify the operational life of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2013· Edwards Lifesciences, LLC

Recalled Item: Proplege Coronary Sinus Catheter model PR9 Recalled by Edwards Lifesciences,...

The Issue: Edwards Lifesciences is recalling certain Proplege Coronary Sinus Catheter,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2013· Mc-NEIL-PPC, Inc.

Recalled Item: KY SilkE Vaginal Moisturizer and Personal Lubricant. The product is Recalled...

The Issue: This product is not cleared for marketing in the US.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2013· Mc-NEIL-PPC, Inc.

Recalled Item: KY TINGLING JELLY Personal Lubricant. The product is packaged into Recalled...

The Issue: This product is not cleared for marketing in the US.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2013· Cenorin, LLC

Recalled Item: HLD System Recalled by Cenorin, LLC Due to The temperature sensor/control...

The Issue: The temperature sensor/control system in the HLD Systems Model 610 may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2013· Stelkast Co

Recalled Item: Stelkast Cross-over Acetabular Shell and Liner Hip System Recalled by...

The Issue: Firm was made aware of incidents relating to the difficulty of properly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2013· Linvatec Corp. dba ConMed Linvatec

Recalled Item: D3000I Advantage Drive System Recalled by Linvatec Corp. dba ConMed Linvatec...

The Issue: The Membrane Switch Panel ( to as "front panel" of the component part number...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 24, 2013· Linvatec Corp. dba ConMed Linvatec

Recalled Item: D3000 Advantage Drive System Recalled by Linvatec Corp. dba ConMed Linvatec...

The Issue: The Membrane Switch Panel ( to as "front panel" of the component part number...

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

Class III — Low RiskOngoing
DrugJanuary 23, 2013· Mission Pharmacal Co

Recalled Item: Sodium Sulfacetamide 10% and Sulfur 5% Lotion Recalled by Mission Pharmacal...

The Issue: Superpotent: Drug product active ingredients were formulated incorrectly...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 23, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Terazosin Hydrochloride Capsules Recalled by Teva Pharmaceuticals USA, Inc....

The Issue: Presence of Foreign Tablets/Capsules: Recall is being conducted due to a...

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

Class II — Potential Health HazardOngoing
Refund