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. 1,921 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,921 in last 12 months

Showing 2502125040 of 53,829 recalls

FoodJanuary 17, 2019· Friendly Fruit Market dba Sid Wainer & Son

Recalled Item: JANSAL VALLEY Cocoa Dusted Chocolate Covered Almonds Recalled by Friendly...

The Issue: Product contains undeclared sesame seeds.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 17, 2019· CryoLife, Inc.

Recalled Item: On-X Aortic Heart Valve with Anatomic Sewing Ring Product Usage: Recalled by...

The Issue: On-X Valve was mislabeled with the incorrect serial number.

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

Class II — Potential Health HazardOngoing
DrugJanuary 16, 2019· KRS Global Biotechnology, Inc

Recalled Item: NORepinephrine 16 mg added to 0.9% Sodium Chloride (PF) Recalled by KRS...

The Issue: Labeling: Label mix-up

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2019· KRS Global Biotechnology, Inc

Recalled Item: NORepinephrine 4 mg added to 5% Dextrose 250 mL Bag (PF) Recalled by KRS...

The Issue: Labeling: Label mix-up

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 16, 2019· Polymer Technology Systems, Inc.

Recalled Item: CHOL+HDL+GLU test strips Recalled by Polymer Technology Systems, Inc. Due to...

The Issue: Some lots of test strips do not fit tightly into the optical block, and may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2019· Polymer Technology Systems, Inc.

Recalled Item: Lipid Panel test strips (as a component of smart bundles) Recalled by...

The Issue: Some lots of test strips do not fit tightly into the optical block, and may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2019· Polymer Technology Systems, Inc.

Recalled Item: Lipid Panel test strips Recalled by Polymer Technology Systems, Inc. Due to...

The Issue: Some lots of test strips do not fit tightly into the optical block, and may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2019· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences(R) IntraClude(TM) Intra-Aortic Occlusion Device is a...

The Issue: Edwards Lifesciences has received a limited number of customer reports...

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

Class II — Potential Health HazardOngoing
DrugJanuary 15, 2019· Tris Pharma Inc.

Recalled Item: infants* IBUPROFEN Recalled by Tris Pharma Inc. Due to Superpotent Drug:...

The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 15, 2019· Tris Pharma Inc.

Recalled Item: Infants' Ibuprofen Recalled by Tris Pharma Inc. Due to Superpotent Drug:...

The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 15, 2019· Tris Pharma Inc.

Recalled Item: Infants' Ibuprofen Recalled by Tris Pharma Inc. Due to Superpotent Drug:...

The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 15, 2019· LUPIN SOMERSET

Recalled Item: Fluocinolone Acetonide Topical Solution Recalled by LUPIN SOMERSET Due to...

The Issue: Failed Impurities/Degradation Specifications: Expansion of October 2018...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 15, 2019· Dr. Reddy's Laboratories, Inc.

Recalled Item: Ezetimibe and Simvastatin Tablets 10mg/80 mg Recalled by Dr. Reddy's...

The Issue: Presence of Foreign Substance: Product complaint of black speckles observed...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 15, 2019· Westmed, Inc.

Recalled Item: Neo-Vent Infant T-Piece Resuscitation Circuit With Infant Mask Recalled by...

The Issue: A repair was made to an adapter mold resulting in parts being produced with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2019· Westmed, Inc.

Recalled Item: Neo-Vent Infant T-Piece Resuscitation Circuit Recalled by Westmed, Inc. Due...

The Issue: A repair was made to an adapter mold resulting in parts being produced with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2019· Westmed, Inc.

Recalled Item: Neo-Vent Infant T-Piece Resuscitation Circuit With Neonatal Mask Recalled by...

The Issue: A repair was made to an adapter mold resulting in parts being produced with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2019· Miami Device Solutions, LLC.

Recalled Item: Proximal Humerus Plate Recalled by Miami Device Solutions, LLC. Due to Right...

The Issue: Right Proximal Humerus Plates. Product component parts MDS130108R, may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2019· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm FDR Go PLUS Recalled by Fujifilm Medical Systems U.S.A., Inc. Due...

The Issue: FUJIFILM Medical Systems U.S.A., Inc., Modality Systems became aware of the...

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

Class II — Potential Health HazardOngoing
FoodJanuary 14, 2019· Century Snacks LLC

Recalled Item: Snak Club Praline Pecans Made With Cane Sugar NET Wt. Recalled by Century...

The Issue: Mis-packaging; product was labeled as Praline Pecans when it was packed with...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 14, 2019· Teleflex Medical

Recalled Item: RUSCH Urinary Drainage bag Recalled by Teleflex Medical Due to The device...

The Issue: The device labels are not UDI compliant. The missing UDI compliance...

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

Class III — Low RiskOngoing