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. 2,840 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,840 in last 12 months

Showing 31613180 of 51,768 recalls

Medical DeviceFebruary 20, 2025· Microbiologics Inc

Recalled Item: Helix Elite" Inactivated Standard: Inactivated SARS-CoV-2 Whole Virus...

The Issue: The A549 human cell target (human cells for sample adequacy control) may...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Wayson Hydrocolloid Models: 1) MJ BANDAGE HYDROCOLLOID HEEL OVAL 6CT...

The Issue: There is a potential for the sterility of the device to be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Wayson Hydrocolloid Models: 1) Model Number: CUR5103 Recalled by MEDLINE...

The Issue: There is a potential for the sterility of the device to be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2025· Calyxo, Inc.

Recalled Item: CVAC Aspiration System Recalled by Calyxo, Inc. Due to Aspiration system,...

The Issue: Aspiration system, for endoscopic examination/treatment of urinary tract and...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 19, 2025· MIM Software Inc

Recalled Item: MIM software Recalled by MIM Software Inc Due to In situations where two...

The Issue: In situations where two images with differing Fields of View (FOV) complete...

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

Class II — Potential Health HazardOngoing
FoodFebruary 18, 2025· Growland Inc

Recalled Item: Dried Longan Pulp- Made in China Recalled by Growland Inc Due to Elevated...

The Issue: Elevated levels of Sulfites in Dried Longan Pulp

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 18, 2025· Turbare Manufacturing

Recalled Item: Avastin 1.25 mg/0.05 mL in 0.25 mL Syringe Recalled by Turbare Manufacturing...

The Issue: Lack of Assurance of Sterility: due to a quality control process deviation....

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 18, 2025· CareFusion 303, Inc.

Recalled Item: BD Alaris Systems Manager Recalled by CareFusion 303, Inc. Due to Software...

The Issue: Software issue that may result in outdated automated programming...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 18, 2025· CareFusion 303, Inc.

Recalled Item: BD Care Coordination Engine (CCE) Infusion Adapter Recalled by CareFusion...

The Issue: Software issue that may result in outdated automated programming...

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

Class I — Serious Health HazardOngoing
DrugFebruary 17, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CURAD Alcohol Prep Pads Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Alcohol Prep Pads Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2025· Safecor Health, LLC

Recalled Item: Ergocalciferol - Vitamin D Supplement - 10 mcg (400 Units) Recalled by...

The Issue: Defective Delivery System: Leakage observed after oral solution was...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2025· Safecor Health, LLC

Recalled Item: Lorazepam 0.5 mg per 0.25 mL Oral Syringe Recalled by Safecor Health, LLC...

The Issue: Defective Delivery System: Leakage observed after oral solution was...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2025· Safecor Health, LLC

Recalled Item: Ferrous Sulfate 7.5 mg Iron/0.5 mL Oral Syringe Recalled by Safecor Health,...

The Issue: Defective Delivery System: Leakage observed after oral solution was...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2025· Safecor Health, LLC

Recalled Item: Morphine Sulfate 5 mg per 0.25 mL Oral Syringe Recalled by Safecor Health,...

The Issue: Defective Delivery System: Leakage observed after oral solution was...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2025· Safecor Health, LLC

Recalled Item: Simethicone 20 mg per 0.3 mL Oral Syringe Recalled by Safecor Health, LLC...

The Issue: Defective Delivery System: Leakage observed after oral solution was...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: Initiation 18 Coated Regular and 18 Coated Super Tampons Recalled by DAYE...

The Issue: Product lacks 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: Initiation 18 Coated Regular and 18 Nude Regular Tampons Recalled by DAYE...

The Issue: Product lacks 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: 18 Coated Regular and 18 Nude Regular Tampons Recalled by DAYE (ANNE'S DAY...

The Issue: Product lacks 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: 3 Month All in One Bundle Recalled by DAYE (ANNE'S DAY LTD) Due to Product...

The Issue: Product lacks 510(k) clearance.

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

Class II — Potential Health HazardOngoing