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. 2,745 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,745 in last 12 months

Showing 1696116980 of 51,768 recalls

Medical DeviceFebruary 22, 2021· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Smart Port CT-Implantable Port Catalogue #: CT96STSD-VI Recalled by...

The Issue: AngioDynamics, Inc. is recalling a specific batch of AngioDynamics...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE¿ FIXED BEARING KNEE - Product Usage: composed of individually...

The Issue: Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+)...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· DePuy Orthopaedics, Inc.

Recalled Item: The ATTUNE¿ Rotating Platform (RP) Total Knee System - Product Recalled by...

The Issue: Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+)...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· DePuy Orthopaedics, Inc.

Recalled Item: The LCS COMPLETE P.F.C.TM SIGMA RP Mobile Bearing Total Knee Recalled by...

The Issue: Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+)...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· Sirtex Medical Limited

Recalled Item: SIROS D-Vial Prep Set Recalled by Sirtex Medical Limited Due to There is a...

The Issue: There is a potential presence of particulate matter in the D-Vial.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Mindray BeneVision Distributed Monitoring System( DMS) 1. p/n 115-051209-00...

The Issue: BeneVision DMS may intermittently freeze and require a manual reboot after...

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

Class II — Potential Health HazardOngoing
DrugFebruary 19, 2021· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Methylprednisolone Tablets USP Recalled by Jubilant Cadista Pharmaceuticals,...

The Issue: Labeling: Illegible label: Customer complaint received of mis-alignment...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 19, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due...

The Issue: Failed Impurities/Degradation Specifications:presence of ATV cyclo IP and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 19, 2021· Noven Pharmaceuticals Inc

Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 30 mg over 9 hours...

The Issue: Defective Delivery System: Out of specification for mechanical peel.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 19, 2021· Noven Pharmaceuticals Inc

Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for mechanical peel.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 19, 2021· Noven Pharmaceuticals Inc

Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for mechanical peel.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 19, 2021· Noven Pharmaceuticals Inc

Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 20 mg over 9 hours...

The Issue: Defective Delivery System: Out of specification for mechanical peel.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 18, 2021· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Acyclovir Sodium Injection 1000mg/20mL (50mg/mL) vial NDC 68382-049-01...

The Issue: Crystallization: customer complaints for crystallization in finished product.

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 18, 2021· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Acyclovir Sodium Injection 500mg/10mL (50mg/mL) vial NDC 68382-048-01...

The Issue: Crystallization: customer complaints for crystallization in finished product.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 18, 2021· Ferrara Candy Company

Recalled Item: Ferrara Candy Company assorted candy Heart Box Recalled by Ferrara Candy...

The Issue: Undeclared ingredients on retail packaging, including but not limited to...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 18, 2021· Sunstar Americas, Inc.

Recalled Item: SUNSTAR G.U.M. HYDRAL DRY MOUTH RELIEF On-the-go Oral Spray Recalled by...

The Issue: The product may be contaminated with Burkholderia cepacia

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2021· Smisson-Cartledge Biomedical, LLC

Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...

The Issue: Customers are being notified of results from a Toxicological Risk Assessment...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 18, 2021· Smisson-Cartledge Biomedical, LLC

Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...

The Issue: Customers are being notified of results from a Toxicological Risk Assessment...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 18, 2021· Smisson-Cartledge Biomedical, LLC

Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...

The Issue: Customers are being notified of results from a Toxicological Risk Assessment...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 18, 2021· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products Calibrator Kit 4-(Calibrator values for TIBC...

The Issue: Potential total iron-binding capacity (TIBC) results. The VITROS TIBC...

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

Class II — Potential Health HazardOngoing