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. 2,765 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,765 in last 12 months

Showing 1558115600 of 51,768 recalls

DrugJuly 30, 2021· Custopharm, Inc.

Recalled Item: FLUDARABINE PHOSPHATE FOR INJECTION Recalled by Custopharm, Inc. Due to Lack...

The Issue: Lack of Assurance of Sterility: the manufacturing firm had microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 30, 2021· Noven Pharmaceuticals Inc

Recalled Item: Combipatch (estradiol/norethindrone acetate transdermal system) 0.05/0.14 mg...

The Issue: Failed Stability Specifications; out of specification for shear.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 30, 2021· Noven Pharmaceuticals Inc

Recalled Item: Combipatch (estradiol/norethindrone acetate transdermal system) 0.05/0.25 mg...

The Issue: Failed Stability Specifications; out of specification for shear.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 30, 2021· Paragon 28, Inc.

Recalled Item: Phantom Nail System Recalled by Paragon 28, Inc. Due to A thin wall...

The Issue: A thin wall condition between the inner cannulation and the flutes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Leica Microsystems, Inc.

Recalled Item: BOND Ready-To-Use Primary Antibody CDX2 (EP25) Recalled by Leica...

The Issue: Product may not perform as specified in IFU.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Getinge Dominican Republic SA

Recalled Item: Arjo Disposable Repositioning Sling Recalled by Getinge Dominican Republic...

The Issue: Sling loop straps on device pose a trip hazard.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Philips North America Llc

Recalled Item: Ingenia Elition X-Magnetic Resonance Medical Electrical Systems indicated...

The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Philips North America Llc

Recalled Item: Ingenia 1.5T-Magnetic Resonance Medical Electrical Systems indicated for use...

The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Philips North America Llc

Recalled Item: Achieva 3.0T-Magnetic Resonance Medical Electrical Systems indicated for use...

The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Philips North America Llc

Recalled Item: Ingenia 1.5T Evoluton- Magnetic Resonance Medical Electrical Systems...

The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Philips North America Llc

Recalled Item: Ingenia 3.0T-Magnetic Resonance Medical Electrical Systems indicated for use...

The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Philips North America Llc

Recalled Item: Ingenia CX 3.0T-Magnetic Resonance Medical Electrical Systems indicated for...

The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Philips North America Llc

Recalled Item: Ingenia Elition S-Magnetic Resonance Medical Electrical Systems indicated...

The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...

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

Class II — Potential Health HazardOngoing
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Cyclobenzaprine Hydrochloride Tablets Recalled by Teva Pharmaceuticals USA...

The Issue: CGMP Deviations: Out of specification (OOS) test result for Total Aerobic...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Cyclobenzaprine Hydrochloride Tablets Recalled by Teva Pharmaceuticals USA...

The Issue: CGMP Deviations: Out of specification (OOS) test result for Total Aerobic...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teligent Pharma, Inc.

Recalled Item: Lidocaine Ointment USP Recalled by Teligent Pharma, Inc. Due to Failed...

The Issue: Failed Viscosity Specifications: lot does not meet specification for...

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

Class III — Low RiskOngoing
Refund
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Cyclobenzaprine Hydrochloride Tablets Recalled by Teva Pharmaceuticals USA...

The Issue: CGMP Deviations: Out of specification (OOS) test result for Total Aerobic...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teligent Pharma, Inc.

Recalled Item: Erythromycin Topical Solution USP Recalled by Teligent Pharma, Inc. Due to...

The Issue: Defective container: possibility for lack of seal integrity.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Epoprostenol Sodium for Injection Recalled by Teva Pharmaceuticals USA Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: DAUNOrubicin Hydrochloride Injection 20 mg/4mL Recalled by Teva...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund