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. 2,017 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
2,017 in last 12 months

Showing 70617080 of 53,829 recalls

Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: : INS7260 / Integra¿ Cranial Access Kit. For access Recalled by Integra...

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: : INS7270 / Integra¿ Cranial Access Kit. For access Recalled by Integra...

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: : HITHSP06 / Integra Cranial Access Kit. For access Recalled by Integra...

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· W.L. Gore & Associates, Inc.

Recalled Item: GORE VIABIL Short Wire Biliary Endoprosthesis Recalled by W.L. Gore &...

The Issue: Devices without transmural drainage holes may be mislabeled as devices with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: : HITHSP04 / Integra Cranial Access Kit. For access Recalled by Integra...

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: : INS7250 / Integra Cranial Access Kit. For access Recalled by Integra...

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
DrugJanuary 19, 2024· Bestco LLC

Recalled Item: Equate Cherry Cough Drops Recalled by Bestco LLC Due to CGMP Deviations:...

The Issue: CGMP Deviations: Potential Glass and Silicone particulates in product

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 19, 2024· OMEZA LLC

Recalled Item: Omeza Lidocaine Lavage pain relief oil 10*2mL VIALS Recalled by OMEZA LLC...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 19, 2024· OMEZA LLC

Recalled Item: Omeza Skin Protectant Recalled by OMEZA LLC Due to CGMP Deviations

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 19, 2024· Bestco LLC

Recalled Item: Family Wellness Cherry Cough Drops Menthol cough suppressant/Oral Anesthetic...

The Issue: CGMP Deviations: Potential Glass and Silicone particulates in product

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 19, 2024· Bestco LLC

Recalled Item: Kroger Cherry Cough Drops Recalled by Bestco LLC Due to CGMP Deviations:...

The Issue: CGMP Deviations: Potential Glass and Silicone particulates in product

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 19, 2024· Bestco LLC

Recalled Item: Meijer Cherry Cough Drops Recalled by Bestco LLC Due to CGMP Deviations:...

The Issue: CGMP Deviations: Potential Glass and Silicone particulates in product

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 19, 2024· Bestco LLC

Recalled Item: CVS Health Cherry Cough Drops Recalled by Bestco LLC Due to CGMP Deviations:...

The Issue: CGMP Deviations: Potential Glass and Silicone particulates in product

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 19, 2024· STRATASYS LTD

Recalled Item: TrueDent Clear Recalled by STRATASYS LTD Due to Customers unable to use...

The Issue: Customers unable to use cartridges due to formatting error in expiration...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 19, 2024· STRATASYS LTD

Recalled Item: TrueDent White Recalled by STRATASYS LTD Due to Customers unable to use...

The Issue: Customers unable to use cartridges due to formatting error in expiration...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 19, 2024· STRATASYS LTD

Recalled Item: TrueDent Magenta Recalled by STRATASYS LTD Due to Customers unable to use...

The Issue: Customers unable to use cartridges due to formatting error in expiration...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 19, 2024· STRATASYS LTD

Recalled Item: TrueDent Yellow Recalled by STRATASYS LTD Due to Customers unable to use...

The Issue: Customers unable to use cartridges due to formatting error in expiration...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 19, 2024· STRATASYS LTD

Recalled Item: TrueDent Cyan Recalled by STRATASYS LTD Due to Customers unable to use...

The Issue: Customers unable to use cartridges due to formatting error in expiration...

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

Class III — Low RiskOngoing
DrugJanuary 18, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Zolpidem Tartrate Extended-Release Tablets Recalled by SUN PHARMACEUTICAL...

The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Febuxostat Tablets 80 mg Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due...

The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...

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

Class II — Potential Health HazardOngoing
Refund