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 2878128800 of 51,768 recalls

DrugOctober 30, 2017· Pharmedium Services, LLC

Recalled Item: ePHEDrine Sulfate In 0.9% Sodium Chloride Recalled by Pharmedium Services,...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 30, 2017· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Meclizine hydrochloride tablets USP Recalled by Jubilant Cadista...

The Issue: Marketed without an approved NDA/ANDA: Bottles were released prior to final...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 28, 2017· NordicNeuroLab AS

Recalled Item: fMRI Hardware System - AudioSystem Recalled by NordicNeuroLab AS Due to...

The Issue: Report was of an interrupted MR scan after patient complained about acoustic...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2017· Physio-Control, Inc.

Recalled Item: LIFEPAK(R) Electrode Starter Kits Recalled by Physio-Control, Inc. Due to...

The Issue: The infant artwork on the product instructs incorrect pad placement. Also,...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 27, 2017· L3 Security & Detection

Recalled Item: L3 Security & Detection System Cabinet X-ray system used for Recalled by L3...

The Issue: L3 has determined in airport environments, there have been several cases...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2017· Physio-Control, Inc.

Recalled Item: LIFEPAK(R) defibrillation electrodes Recalled by Physio-Control, Inc. Due to...

The Issue: The infant artwork on the product instructs incorrect pad placement. Also,...

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

Class I — Serious Health HazardOngoing
DrugOctober 27, 2017· Fresenius Kabi USA, LLC

Recalled Item: Midazolam Injection Recalled by Fresenius Kabi USA, LLC Due to Labeling:...

The Issue: Labeling: Label MIX-UP. Blister Packages, Labeled as Midazolam injection,...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· ConvaTec, Inc

Recalled Item: SUR-FIT Natura Moldable Durahesive Skin Barrier with Hydrocolloid Flexible...

The Issue: A portion of Lot 7H02242 outer boxes (market units) of the SUR-FIT Natura...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Arterial Access Tray Recalled by Arrow International Inc Due to The povidone...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2017· Zimmer Biomet, Inc.

Recalled Item: A.L.P.S. MIS Calcaneus Locking Plate LG RT F.A.S.T. Guide inserts Recalled...

The Issue: The drill guides were manufactured with the incorrect color anodization.

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

Class II — Potential Health HazardOngoing
FoodOctober 25, 2017· E & E Enterprises

Recalled Item: Cheesey Bacon Dip Recalled by E & E Enterprises Due to Ingredients statement...

The Issue: Ingredients statement declared whey, powdered cheese and cheddar cheese but...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 25, 2017· E & E Enterprises

Recalled Item: Cheesey Pizza Dip Recalled by E & E Enterprises Due to Ingredients statement...

The Issue: Ingredients statement declared whey, powdered cheese and cheddar cheese but...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 25, 2017· Teva Pharmaceuticals USA

Recalled Item: Dutasteride and Tamsulosin HCl Capsules Recalled by Teva Pharmaceuticals USA...

The Issue: Failed dissolution specifications; all lots within expiry are being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 25, 2017· Fagron, Inc

Recalled Item: Estriol Recalled by Fagron, Inc Due to cGMP Deviations: lack of quality...

The Issue: cGMP Deviations: lack of quality assurance at the API manufacturer.

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

Class II — Potential Health HazardOngoing
Refund