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. 2,624 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,624 in last 12 months

Showing 2872128740 of 51,768 recalls

Medical DeviceNovember 10, 2017· Zevex Incorporated (dba Moog Medical Medical Devices Group)

Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...

The Issue: Particulate found on the Curlin spike.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2017· Zevex Incorporated (dba Moog Medical Medical Devices Group)

Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...

The Issue: Particulate found on the Curlin spike.

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

Class II — Potential Health HazardOngoing
FoodNovember 10, 2017· New Century Snacks LLC

Recalled Item: Happy Belly Deluxe Mixed Nuts - roasted and salted with sea salt. Cashews...

The Issue: Firm was notified by customer that the back panel (ingredients and nutrition...

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

Class III — Low RiskOngoing
Refund
FoodNovember 10, 2017· New Century Snacks LLC

Recalled Item: Happy Belly Cranberry & Nuts Trail Mix - dried cranberries Recalled by New...

The Issue: Firm was notified by customer that the back panel (ingredients and nutrition...

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

Class III — Low RiskOngoing
Refund
FoodNovember 9, 2017· Figi's, Inc

Recalled Item: Dark Chocolate covered Gingersnaps. Packaged as follows: 1. in clear...

The Issue: Figi's is recalling Gift #0368 Christmas Gingersnap Variety and Bulk Dark...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2017· Mayne Pharma Inc

Recalled Item: Liothyronine Sodium Tablets Recalled by Mayne Pharma Inc Due to Failed...

The Issue: Failed Dissolution Specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2017· Teva Pharmaceuticals USA

Recalled Item: Clozapine Tablets USP Recalled by Teva Pharmaceuticals USA Due to Failed...

The Issue: Failed Tablet/Capsule Specifications; potential presence of broken tablets.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2017· Kareway Products Inc

Recalled Item: GERICARE Eyewash Recalled by Kareway Products Inc Due to Non-sterility:...

The Issue: Non-sterility: confirmed microbial contamination with Achromobacter xylosoxidans

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 9, 2017· Vascular Insights, LLC

Recalled Item: ClariVein IC infusion catheter Recalled by Vascular Insights, LLC Due to...

The Issue: Certain catheters could have a compromised catheter shaft due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista System LOCI 8 CALIBRATOR The LOCI 8 Calibrator Recalled by...

The Issue: An increase in the number of failed calibration events or negative bias with...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2017· Bard Medical Division

Recalled Item: Medivance(R) ARCTIC SUN(R) ARCTICGEL(TM) Pads: Description Recalled by Bard...

The Issue: Specific lots of ArcticGel Pads have potential issues which may result in...

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

Class II — Potential Health HazardOngoing
DrugNovember 8, 2017· L. Perrigo Company

Recalled Item: Maximum Strength Zephrex-D Recalled by L. Perrigo Company Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 7, 2017· Dominguez Family Enterprises, Inc

Recalled Item: Juanita's Brand OJOS Mexican Pastry. Product are pink balls of Recalled by...

The Issue: Juanita 's Brand OJOS Mexican Pastry, 6 counts in plastic bag, is recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2017· Claris Lifesciences Inc

Recalled Item: Ciprofloxacin in Dextrose (5%) Injection Recalled by Claris Lifesciences Inc...

The Issue: Superpotent

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

Class III — Low RiskOngoing
Refund
DrugNovember 6, 2017· West-Ward Pharmaceuticals Corp.

Recalled Item: Dexamethasone Sodium Phosphate Injection Recalled by West-Ward...

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

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

Class III — Low RiskOngoing
Refund
DrugNovember 6, 2017· West-Ward Pharmaceuticals Corp.

Recalled Item: Dexamethasone Sodium Phosphate Injection Recalled by West-Ward...

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

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 6, 2017· Boston Scientific Corporation

Recalled Item: Innova Self-Expanding Stent System Recalled by Boston Scientific Corporation...

The Issue: Stent possibly unable to be fully released from the delivery system.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2017· CareFusion 303, Inc.

Recalled Item: Alaris Extension Sets with microbore tubing Model 20022 and 30914 Recalled...

The Issue: Reports of incorrect priming volume due to manufacturing with incorrect tubing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2017· Owen Mumford USA, Inc.

Recalled Item: Unifine Pentips 5mm x 31G pen needles Recalled by Owen Mumford USA, Inc. Due...

The Issue: Device may potentially be compromised by water in end user packaging....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2017· Owen Mumford USA, Inc.

Recalled Item: Unifine Pentips 5mm x 31G pen needles Recalled by Owen Mumford USA, Inc. Due...

The Issue: Device may potentially be compromised by water in end user packaging....

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

Class II — Potential Health HazardOngoing