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. 1,898 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,898 in last 12 months

Showing 2748127500 of 53,829 recalls

Medical DeviceJuly 6, 2018· Smiths Medical ASD Inc.

Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...

The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...

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

Class III — Low RiskOngoing
Medical DeviceJuly 6, 2018· Smiths Medical ASD Inc.

Recalled Item: smiths medical portex First Breath Nasal Oxygen Cannula Recalled by Smiths...

The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...

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

Class III — Low RiskOngoing
Medical DeviceJuly 6, 2018· Smiths Medical ASD Inc.

Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...

The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...

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

Class III — Low RiskOngoing
Medical DeviceJuly 6, 2018· Smiths Medical ASD Inc.

Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...

The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...

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

Class III — Low RiskOngoing
Medical DeviceJuly 6, 2018· Smiths Medical ASD Inc.

Recalled Item: smiths medical portex First Breath Nasal Oxygen Cannula Recalled by Smiths...

The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...

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

Class III — Low RiskOngoing
Medical DeviceJuly 6, 2018· Neotract Inc

Recalled Item: UroLift System Number: UL400-4 Tray Contents: UroLift System Recalled by...

The Issue: Upon implant deployment, the Capsular Tab may not be delivered as the needle...

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

Class II — Potential Health HazardOngoing
DrugJuly 5, 2018· Sanofi-Aventis U.S. LLC

Recalled Item: Admelog Solostar (insulin lispro injection) Recalled by Sanofi-Aventis U.S....

The Issue: Temperature Abuse: Product samples of Admelog may not have been shipped at...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 5, 2018· The Hain Celestial Group, Inc. - Worldwide HQ

Recalled Item: alba BOTANICA sport mineral sunscreen (titanium dioxide 7.0% and zinc...

The Issue: Incorrect Product Formulation: wrong sunscreen product in the package.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 5, 2018· Teva Pharmaceuticals USA

Recalled Item: Fluocinolone Acetonide Topical Solution Recalled by Teva Pharmaceuticals USA...

The Issue: Failed Impurities and Degradation Specifications and Subpotent Drug:...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 5, 2018· Gourmet International Inc.

Recalled Item: SPARKLING SOUR CHERRY JUICE DRINK Recalled by Gourmet International Inc. Due...

The Issue: Gourmet International Inc. is voluntarily recalling LItaly Sparkling Juice...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 5, 2018· Gourmet International Inc.

Recalled Item: SPARKLING POMEGRANETE JUICE DRNK Recalled by Gourmet International Inc. Due...

The Issue: Gourmet International Inc. is voluntarily recalling LItaly Sparkling Juice...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 5, 2018· Gourmet International Inc.

Recalled Item: SPARKLING MANDARIN JUICE DRINK Recalled by Gourmet International Inc. Due to...

The Issue: Gourmet International Inc. is voluntarily recalling LItaly Sparkling Juice...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 5, 2018· Gourmet International Inc.

Recalled Item: SPARKLING GRAPEFRUIT JUICE DRINK Recalled by Gourmet International Inc. Due...

The Issue: Gourmet International Inc. is voluntarily recalling LItaly Sparkling Juice...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 5, 2018· Gourmet International Inc.

Recalled Item: SPARKLING LEMON JUICE DRINK Recalled by Gourmet International Inc. Due to...

The Issue: Gourmet International Inc. is voluntarily recalling LItaly Sparkling Juice...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 5, 2018· Gourmet International Inc.

Recalled Item: SPARKLING LIME JUICE DRINK Recalled by Gourmet International Inc. Due to...

The Issue: Gourmet International Inc. is voluntarily recalling LItaly Sparkling Juice...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 3, 2018· Medgyn Products, Inc.

Recalled Item: Monsel's Solution (Ferric Subsulfate) Recalled by Medgyn Products, Inc. Due...

The Issue: CGMP Deviations: The manufacturer of this product recalled because they were...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 3, 2018· Radiometer America Inc

Recalled Item: ABL800 analyzer Recalled by Radiometer America Inc Due to The analyzer...

The Issue: The analyzer software may cause a mis-match of patient demographics and test...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2018· ConvaTec, Inc

Recalled Item: AbViser AutoValve IAP (intra- abdominal pressure) Monitoring Device Recalled...

The Issue: Bubble Leak Testing on AbViser AutoValve IAP Monitoring Devices without...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2018· Arrow International Inc

Recalled Item: Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip...

The Issue: One lot of product is from product code AK-22502 so it contains a 2-lumen, 5...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2018· Abbott Vascular

Recalled Item: PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recommended Recalled...

The Issue: Incorrect expiration being entered for one lot.

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

Class II — Potential Health HazardOngoing