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. 1,003 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,003 in last 12 months

Showing 35401–35420 of 53,829 recalls

Medical DeviceAugust 5, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.x picture archiving and communication system Syngo.x is a software...

The Issue: Software error. Incorrect values for the volume calculation from a freehand...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.via picture archiving and communication system Syngo via is a Recalled...

The Issue: Software error. Incorrect values for the volume calculation from a freehand...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Medtronic Inc.

Recalled Item: CareLink iPro Version 1.10 Recalled by Medtronic Inc. Due to Medtronic...

The Issue: Medtronic MiniMed is recalling the CareLink iPro Therapy Management Software...

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

Class II — Potential Health HazardOngoing
FoodAugust 5, 2016· Sprouts Extraordinaire, LLC

Recalled Item: 5 lb Living Alfalfa Sprouts. One package per case. Distributed Recalled by...

The Issue: Sprouts Extraordinaire, LLC is recalling 5 lb Living Alfalfa Sprout cases...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 4, 2016· Level Ground Trading Limited

Recalled Item: Organic Cacao Nibs Recalled by Level Ground Trading Limited Due to Product...

The Issue: Product may contain glass fragments

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

Class III — Low RiskOngoing
Refund
DrugAugust 4, 2016· Amerisource Health Services

Recalled Item: buPROPion Hydrochloride Extended-Release Tablets Recalled by Amerisource...

The Issue: Failed dissolution specifications - the out of specification result for...

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

Class III — Low RiskOngoing
Refund
DrugAugust 4, 2016· Hospira Inc., A Pfizer Company

Recalled Item: Bupivacaine Hydrochloride Inj. Recalled by Hospira Inc., A Pfizer Company...

The Issue: Presence of particulate matter: Confirmed customer report for the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 4, 2016· Genzyme Corporation / Genzyme Biosurgery

Recalled Item: Mozobil (plerixafor injection) 24 mg/1.2 mL (20 mg/mL) per vial Recalled by...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 4, 2016· Beckman Coulter Inc.

Recalled Item: UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System Recalled by...

The Issue: Beckman Coulter is recalling the UniCel DxH Slidemaker Stainer Coulter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2016· Integra LifeSciences Corp. d.b.a. Integra Pain Management

Recalled Item: INTEGRA Spinal Tray Recalled by Integra LifeSciences Corp. d.b.a. Integra...

The Issue: Integra LifeSciences is recalling Spinal Trays, Cat No. 3404875, because of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2016· Terumo Medical Corp

Recalled Item: MISAGO RX Self Expanding Peripheral Stem Recalled by Terumo Medical Corp Due...

The Issue: During recent routine testing, the MISAGO Peripheral Stent was found not to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· LeMaitre Vascular, Inc.

Recalled Item: 1.5 mm HYDRO LeMaitre Valvulotome Recalled by LeMaitre Vascular, Inc. Due to...

The Issue: Wire which deploys the loop may be come detached at the handle causing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· C.R. Bard, Inc.

Recalled Item: BARD¿ 70cc Piston Syringe with Catheter Tip Recalled by C.R. Bard, Inc. Due...

The Issue: Package Defect: Products may be at risk for having a slit defect on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· C.R. Bard, Inc.

Recalled Item: BARD¿ Irrigation Recalled by C.R. Bard, Inc. Due to Package Defect: Products...

The Issue: Package Defect: Products may be at risk for having a slit defect on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· C.R. Bard, Inc.

Recalled Item: BARD¿ Piston Syringe Recalled by C.R. Bard, Inc. Due to Package Defect:...

The Issue: Package Defect: Products may be at risk for having a slit defect on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· C.R. Bard, Inc.

Recalled Item: BARDIA¿ 60cc Piston Irrigation Syringe Recalled by C.R. Bard, Inc. Due to...

The Issue: Package Defect: Products may be at risk for having a slit defect on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ Calcium (CA) Flex¿ reagent cartridge Device Listing No.:...

The Issue: Siemens Healthcare Diagnostics determined that the Dimension Vista Calcium...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· LeMaitre Vascular, Inc.

Recalled Item: 1.5 mm HYDRO LeMaitre Valvulotome Recalled by LeMaitre Vascular, Inc. Due to...

The Issue: Wire which deploys the loop may be come detached at the handle causing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· LeMaitre Vascular, Inc.

Recalled Item: 1.5 mm HYDRO LeMaitre Valvulotome without LeMills Recalled by LeMaitre...

The Issue: Wire which deploys the loop may be come detached at the handle causing the...

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

Class II — Potential Health HazardOngoing
FoodAugust 3, 2016· Whole Foods Market

Recalled Item: Grassfields Onion N Garlic Cheese Recalled by Whole Foods Market Due to...

The Issue: Possible contamination with Shiga toxin-producing E. coli (STEC).

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

Class I — Serious Health HazardOngoing
Refund