Product Recalls in Virginia

Product recalls affecting Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,813 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
2,813 in last 12 months

Showing 69216940 of 53,829 recalls

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
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· Howmedica Osteonics Corp.

Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM Recalled by Howmedica Osteonics...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM Recalled by Howmedica Osteonics...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: X3 TRIATHLON CS INSERT NO 6 10 MM Recalled by Howmedica Osteonics Corp. Due...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: X3 TRIATHLON CS INSERT NO 3 10 MM Recalled by Howmedica Osteonics Corp. Due...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing