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. 1,777 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,777 in last 12 months

Showing 4646146480 of 51,768 recalls

Medical DeviceAugust 29, 2013· Vital Diagnostics, Inc.

Recalled Item: Consult Diagnostics¿ Eon Calcium Reagent For In-Vitro Diagnostic Use PN:...

The Issue: High positive calcium bias on plasma sample versus results on serum

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Boston Scientific CRM Corp

Recalled Item: Boston Scientific TELIGEN Recalled by Boston Scientific CRM Corp Due to The...

The Issue: The performance of a low voltage capacitor in a subset of COGNIS CRT-Ds and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Steris Corporation

Recalled Item: Reliance Endoscope Processing System (REPS) Recalled by Steris Corporation...

The Issue: The air pipe that delivers unfiltered ambient air from the procedure room...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: Combiset Blood Line Hemodialysis use Catalog Number: 03-2622-3. Intended for...

The Issue: Updated Instructions for Use: Bloodline connections not tightened per...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Carestream Health Inc.

Recalled Item: DRX- Revolution Recalled by Carestream Health Inc. Due to Carestream Health...

The Issue: Carestream Health Inc. has conducted a voluntary field action which includes...

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

Class II — Potential Health HazardOngoing
DrugAugust 29, 2013· Dr. Reddy's Laboratories, Inc.

Recalled Item: IBU (TM) IBUPROFEN Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Labeling: Incorrect or missing lot and/or exp date- This product is being...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2013· Procter & Gamble Co

Recalled Item: Vicks NyQuil Cold and Flu Nighttime Relief Recalled by Procter & Gamble Co...

The Issue: Incorrect/ Undeclared Excipients: NyQuil Liquid Original bottles were...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2013· Cubist Pharmaceuticals, Inc.

Recalled Item: Cubicin (daptomycin for injection) Recalled by Cubist Pharmaceuticals, Inc....

The Issue: Presence of Particulate Matter; Glass particulates observed in vials

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 29, 2013· Hospira Inc.

Recalled Item: 5% Lidocaine HCl and 7.5% Dextrose Injection Recalled by Hospira Inc. Due to...

The Issue: Presence of Particulate Matter; report of visible particulates in the glass...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 28, 2013· SpineFrontier, Inc.

Recalled Item: S-LIFT Extension Shims Extension shims are manufactured from grade 5...

The Issue: Fit variation among all lots of S-LIFT extension shims with corresponding...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2013· Globus Medical, Inc.

Recalled Item: Globus Medical MicroFuse Putty Recalled by Globus Medical, Inc. Due to The...

The Issue: The sterility of this product to a Sterility Assurance Level (SAL) of 10(-6)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens RAD Fluoro Uro System (Ysio Recalled by Siemens Medical Solutions...

The Issue: When using systems operating with software versions VD10A/G during a RAD...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2013· Zimmer, Inc.

Recalled Item: VerSys¿ Cemented Revision Calcar (CRC) Hip System Femoral Stems VerSys...

The Issue: Based on a review of historic packaging validations, it was determined that...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2013· Carefusion 2200 Inc

Recalled Item: *** 1) Cat. 4341B Recalled by Carefusion 2200 Inc Due to Catheters included...

The Issue: Catheters included in Thoracentesis Tray and Safe-T Thoracentesis Tray -...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

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

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 27, 2013· Siemens Healthcare Diagnostics

Recalled Item: T3F Recalled by Siemens Healthcare Diagnostics Due to Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics confirmed customer complaints regarding an...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2013· H & H Associates

Recalled Item: H&H Emergency Cricothyrotomy Kit (Part No. HHECT01/ HHECTK01 Recalled by H &...

The Issue: Medical device tubing used for endotracheal airway application may become...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 27, 2013· Clark Laboratories, Inc. (dba,Trinity Biotech USA)

Recalled Item: Captia Syphilis-G Test Kit Product Usage: This is an enzyme Recalled by...

The Issue: Trinity Biotech recalled Trinity Biotech Captia Syphilis IgG kits due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2013· Siemens Healthcare Diagnostics

Recalled Item: T3F Recalled by Siemens Healthcare Diagnostics Due to Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics confirmed customer complaints regarding an...

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

Class II — Potential Health HazardOngoing
FoodAugust 27, 2013· Snoqualmie Falls Candy Factory, LLC

Recalled Item: Coconut Peanut Brittle's label is read in parts:"***COCONUT PEANUT...

The Issue: Finished product labels declared butter or cream but milk is not listed.

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

Class II — Potential Health HazardOngoing
Refund