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. 2,486 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,486 in last 12 months

Showing 4134141360 of 51,768 recalls

DrugJanuary 28, 2015· Pharmedium Services, LLC

Recalled Item: Bupivacaine HCl 0.0625% Recalled by Pharmedium Services, LLC Due to Presence...

The Issue: Presence of Particulate Matter: The firm manufactured products using Hospira...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 28, 2015· Pharmedium Services, LLC

Recalled Item: Morphine Sulfate Recalled by Pharmedium Services, LLC Due to Presence of...

The Issue: Presence of Particulate Matter: The firm manufactured products using Hospira...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 28, 2015· Akorn, Inc.

Recalled Item: Erythromycin Pledgets USP Recalled by Akorn, Inc. Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: Active Pharmaceutical...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 28, 2015· Medical Components, Inc dba MedComp

Recalled Item: 9F Plastic Dual Port Recalled by Medical Components, Inc dba MedComp Due to...

The Issue: The dual port with catheters was not covered under FDA clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2015· Zimmer, Inc.

Recalled Item: Persona Trabecular Metal Tibial Plate / Persona TM Tibia-Prosthesis Recalled...

The Issue: An increase in complaints of loosening and radiolucent lines.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2015· GE Healthcare

Recalled Item: GE Healthcare Engstrom Carestation Recalled by GE Healthcare Due to...

The Issue: Potential failure of the caster mounting hardware, which may result in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems Progesterone Kit Recalled by Siemens Healthcare...

The Issue: ADVIA Centaur Systems Progesterone Kit Lots Ending in 268 have a high bias...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems Progesterone Kit Recalled by Siemens Healthcare...

The Issue: ADVIA Centaur Systems Progesterone Kit Lots Ending in 268 have a high bias...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems Progesterone Kit Recalled by Siemens Healthcare...

The Issue: ADVIA Centaur Systems Progesterone Kit Lots Ending in 268 have a high bias...

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

Class II — Potential Health HazardOngoing
DrugJanuary 26, 2015· AnazaoHealth Corporation

Recalled Item: Compounded Plaquex Recalled by AnazaoHealth Corporation Due to Good...

The Issue: Good Manufacturing Practices Deviations: The product has an active...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 26, 2015· CooperSurgical, Inc.

Recalled Item: MediChoice WarmGel Infant Heel Warmer Recalled by CooperSurgical, Inc. Due...

The Issue: Products without expiration date have the remote potential for minor burn

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2015· CooperSurgical, Inc.

Recalled Item: CooperSurgical Infant Heel Gel Warmers Recalled by CooperSurgical, Inc. Due...

The Issue: Products without expiration date have the remote potential for minor burn

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2015· CooperSurgical, Inc.

Recalled Item: Fisher Brand Gel Infant Heel Gel Warmers Recalled by CooperSurgical, Inc....

The Issue: Products without expiration date have the remote potential for minor burn

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2015· CooperSurgical, Inc.

Recalled Item: NovaPlus Brand Warm Gel Infant Heel Gel Warmer Recalled by CooperSurgical,...

The Issue: Products without expiration date have the remote potential for minor burn

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

Class II — Potential Health HazardOngoing
DrugJanuary 25, 2015· Detox Transforms

Recalled Item: EDGE Amplified Weight Release capsules Recalled by Detox Transforms Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 25, 2015· Detox Transforms

Recalled Item: BtRiM Max capsules Recalled by Detox Transforms Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 25, 2015· Detox Transforms

Recalled Item: iNDiGO capsules Recalled by Detox Transforms Due to Undeclared Phenolphthalein

The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 25, 2015· Detox Transforms

Recalled Item: AMPD GOLD Bee Pollen capsules Recalled by Detox Transforms Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 25, 2015· Detox Transforms

Recalled Item: iNSANE Bee Pollen capsules Recalled by Detox Transforms Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 23, 2015· Hospira Inc.

Recalled Item: KETOROLAC Tromethamine Inj. Recalled by Hospira Inc. Due to Crystallization

The Issue: Crystallization

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

Class II — Potential Health HazardOngoing
Refund