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. 2,805 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,805 in last 12 months

Showing 68616880 of 51,768 recalls

Medical DeviceFebruary 7, 2024· Beckman Coulter, Inc.

Recalled Item: Access Substrate Recalled by Beckman Coulter, Inc. Due to On 07 February...

The Issue: On 07 February 2024 Beckman Coulter made the decision to conduct a field...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2024· Natus Neurology Inc

Recalled Item: TENSIVE Conductive Adhesive Gel Recalled by Natus Neurology Inc Due to Natus...

The Issue: Natus has become aware that its third-party supplier Parker Laboratories...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2024· Smiths Medical ASD Inc.

Recalled Item: smiths medical Pneupac paraPAC plus 310 ventilator kit with PEEP and CPAP...

The Issue: When a paraPAC plus ventilator is switched to the operating mode of...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 7, 2024· Smiths Medical ASD Inc.

Recalled Item: smiths medical Pneupac paraPAC plus 300 ventilator kit without PEEP and CPAP...

The Issue: When a paraPAC plus ventilator is switched to the operating mode of...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 7, 2024· Natus Neurology Inc

Recalled Item: natus neurology Recalled by Natus Neurology Inc Due to Natus has become...

The Issue: Natus has become aware that its third-party supplier Parker Laboratories...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: DCA Systems HbA1c Reagent Kit Recalled by Siemens Healthcare Diagnostics,...

The Issue: The reason for the recall is that the Siemens DCA HbA1c Reagent Kit was...

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

Class II — Potential Health HazardOngoing
FoodFebruary 6, 2024· Reser's Fine Foods, Inc.

Recalled Item: Item # 407034 Recalled by Reser's Fine Foods, Inc. Due to Potential Listeria...

The Issue: Listeria monocytogenes. The recalled Cotija cheese was repackaged into...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 6, 2024· Reser's Fine Foods, Inc.

Recalled Item: Item 404764 Recalled by Reser's Fine Foods, Inc. Due to Potential Listeria...

The Issue: Listeria monocytogenes. The recalled Cotija cheese was repackaged into...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 6, 2024· Reser's Fine Foods, Inc.

Recalled Item: FCF Item 403949 Recalled by Reser's Fine Foods, Inc. Due to Potential...

The Issue: Listeria monocytogenes. The recalled Cotija cheese was repackaged into...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 6, 2024· Reser's Fine Foods, Inc.

Recalled Item: FCF Item 403953 Recalled by Reser's Fine Foods, Inc. Due to Potential...

The Issue: Listeria monocytogenes. The recalled Cotija cheese was repackaged into...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 6, 2024· Reser's Fine Foods, Inc.

Recalled Item: FCF Item 406957 Recalled by Reser's Fine Foods, Inc. Due to Potential...

The Issue: Listeria monocytogenes. The recalled Cotija cheese was repackaged into...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 6, 2024· Reser's Fine Foods, Inc.

Recalled Item: FCF Item #404967 Recalled by Reser's Fine Foods, Inc. Due to Potential...

The Issue: Listeria monocytogenes. The recalled Cotija cheese was repackaged into...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 6, 2024· Mallinckrodt Hospital Products Inc.

Recalled Item: Acthar Gel (repository corticotropin injection) 400 USP units/5mL (80 USP...

The Issue: cGMP deviations: Temperature excursion due to shipping delay from...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2024· Mallinckrodt Hospital Products Inc.

Recalled Item: Terlivaz (terlipressin for injection) Recalled by Mallinckrodt Hospital...

The Issue: cGMP deviations: Temperature excursion due to shipping delay from...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2024· Today The World

Recalled Item: Arize Herbal Dietary Supplement Recalled by Today The World Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 6, 2024· Today The World

Recalled Item: SCHWINNNG Herbal Dietary Supplement Recalled by Today The World Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 6, 2024· Today The World

Recalled Item: Sustain Herbal Dietary Supplement Recalled by Today The World Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to be...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 6, 2024· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...

The Issue: Due to two complaints, has come to our attention that additional guidance is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...

The Issue: Due to two complaints, has come to our attention that additional guidance is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...

The Issue: Due to two complaints, has come to our attention that additional guidance is...

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

Class II — Potential Health HazardOngoing