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. 2,794 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,794 in last 12 months

Showing 1028110300 of 51,768 recalls

Medical DeviceMarch 1, 2023· Atrium Medical Corporation

Recalled Item: Atrium Pneumostat Chest Drain Valve Recalled by Atrium Medical Corporation...

The Issue: The Instructions for Use (IFU) for the Pneumostat Chest Drain Valve and the...

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

Class II — Potential Health HazardOngoing
DrugFebruary 28, 2023· Sagent Pharmaceuticals Inc

Recalled Item: Heparin Sodium Injection Recalled by Sagent Pharmaceuticals Inc Due to...

The Issue: Labeling: Not elsewhere classified

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 28, 2023· BA Sports Nutrition, LLC

Recalled Item: BODYARMOR SportWater 24/700mL Recalled by BA Sports Nutrition, LLC Due to...

The Issue: Potential for plastic pieces in product

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 28, 2023· Omega Medical Imaging, Inc.

Recalled Item: Omega Medical Imaging Elevating Monitor Suspension Recalled by Omega Medical...

The Issue: An actuator separated from the pivot mechanism on a lower monitor boom...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2023· Bio-Rad Laboratories, Inc.

Recalled Item: BioPlex 2200 Recalled by Bio-Rad Laboratories, Inc. Due to APLS IgM reagent...

The Issue: APLS IgM reagent kits were packaged with the incorrect conjugate, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2023· Encore Medical, LP

Recalled Item: EMPOWR Porous Knee Patella Over Drill Recalled by Encore Medical, LP Due to...

The Issue: Patella drills are marked with incorrect diameter size of 5.6mm, when they...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2023· Bard Peripheral Vascular Inc

Recalled Item: Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM Recalled by...

The Issue: The external diameter of the biopsy instrument is larger than the internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2023· Elekta Inc

Recalled Item: Monaco RTP System. Used to make treatment plans for patients Recalled by...

The Issue: Re-optimization, after adding contours without forced density outside the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2023· FUJIFILM Healthcare Americas Corporation

Recalled Item: FujiFilm FDR AQRO (Model DR-XD1000)- A digital mobile X-ray system Recalled...

The Issue: Arm which holds the tube head in place is susceptible to breaking, if the...

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

Class II — Potential Health HazardOngoing
DrugFebruary 24, 2023· Global Pharma Healthcare Private Limited

Recalled Item: Delsam Pharma's Artificial Eye Ointment (Mineral Oil 15% Recalled by Global...

The Issue: Non-Sterility: FDA analysis found unopened tubes to be contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 24, 2023· Ecometics, Inc.

Recalled Item: Unguentine Original Maximum Strength Pain Relieving/Antiseptic Ointment...

The Issue: CGMP DEVIATIONS

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 24, 2023· Ecometics, Inc.

Recalled Item: Alcolado Relampago (menthol 1% Recalled by Ecometics, Inc. Due to CGMP...

The Issue: CGMP DEVIATIONS

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 24, 2023· Ecometics, Inc.

Recalled Item: Activator Concentrate (sodium fluoride 0.96% in Activator) 1 fl. Oz Recalled...

The Issue: CGMP DEVIATIONS

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 24, 2023· Ecometics, Inc.

Recalled Item: Vencedor medicated balm (capsaicin 0.028%) 1.5 oz. (43g) tubes Recalled by...

The Issue: CGMP DEVIATIONS

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 24, 2023· Ecometics, Inc.

Recalled Item: Unguentine Original Ointment for Burns (Camphor 3.0% Recalled by Ecometics,...

The Issue: CGMP DEVIATIONS

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 24, 2023· Ecometics, Inc.

Recalled Item: Soltice Quick-RUB (Menthol 5.1% Recalled by Ecometics, Inc. Due to CGMP...

The Issue: CGMP DEVIATIONS

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 24, 2023· Ecometics, Inc.

Recalled Item: Nose Better Gel (0.75% Camphor Recalled by Ecometics, Inc. Due to CGMP...

The Issue: CGMP DEVIATIONS

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 24, 2023· SCA Pharmaceuticals

Recalled Item: Fentanyl 1 Recalled by SCA Pharmaceuticals Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 24, 2023· Tobii Dynavox Llc

Recalled Item: Tobii Dynavox TD I-110 Speech Device-tablet style speech generating device...

The Issue: Problem maintaining the stable placement of the battery may come loose from...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2023· Iradimed Corporation

Recalled Item: Iradimed Corporation MRidium MRI 1000 Series Infusion Sets Recalled by...

The Issue: Certain Iradimed 1057 Syringe Adapter Sets, used with the MRidium MRI...

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

Class II — Potential Health HazardOngoing