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. 1,936 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,936 in last 12 months

Showing 2072120740 of 53,829 recalls

Medical DeviceJanuary 22, 2020· Braemar Manufacturing, LLC

Recalled Item: Braemar Manufacturing LLC DL900 Holter Monitor 1285 Corporate Center Dr....

The Issue: An issue with the DL900 and DL950 Series Holter Recorder was recognized on...

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

Class II — Potential Health HazardOngoing
FoodJanuary 21, 2020· ABH Nature's Products, Inc.

Recalled Item: All Dietary Supplement manufactured and distributed by ABH Nature's Products...

The Issue: Firm ordered by consent decree to recall all products because the products...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 21, 2020· Aesculap Implant Systems LLC

Recalled Item: Columbus R/PS TIB.PLATEAU Cemented Recalled by Aesculap Implant Systems LLC...

The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2020· Aesculap Implant Systems LLC

Recalled Item: COLUMBUS CRA/PSA TIB.PLAT.CEMENTED Recalled by Aesculap Implant Systems LLC...

The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2020· Aesculap Implant Systems LLC

Recalled Item: COLUMBUS CR/PS TIB.PLAT.PLASMAPORE Recalled by Aesculap Implant Systems LLC...

The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2020· Aesculap Implant Systems LLC

Recalled Item: AS COLUMBUS CR/PS TIB.PLAT.CEMENTED Recalled by Aesculap Implant Systems LLC...

The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2020· Aesculap Implant Systems LLC

Recalled Item: COLUMBUS REV F TIBIA OFFSET CEMENTED Recalled by Aesculap Implant Systems...

The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2020· Polymer Technology Systems, Inc.

Recalled Item: PTS Detect Cotinine Recalled by Polymer Technology Systems, Inc. Due to The...

The Issue: The firm is removing the product from the market after discussions with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2020· Hologic, Inc.

Recalled Item: Selenia Dimensions Mammography System Recalled by Hologic, Inc. Due to The...

The Issue: The recalling firm has received reports from the field of the C-arm on the...

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

Class II — Potential Health HazardOngoing
DrugJanuary 20, 2020· Macleods Pharma Usa Inc

Recalled Item: Montelukast Sodium Chewable Tablets Recalled by Macleods Pharma Usa Inc Due...

The Issue: Failed Dissolution Specifications: testing revealed low out of specification...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 19, 2020· EHOB, Inc.

Recalled Item: Econocare Plus Overlay Item: 1025EC. Intended to aid in the Recalled by...

The Issue: Due to a nonconformance of product contamination (human blood) of Econocare...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Kentec Medical, Inc

Recalled Item: Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes....

The Issue: Feeding tube plastic tethered closure cap may possibly fracture or break....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Kentec Medical, Inc

Recalled Item: Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes....

The Issue: Feeding tube plastic tethered closure cap may possibly fracture or break....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Kentec Medical, Inc

Recalled Item: Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes....

The Issue: Feeding tube plastic tethered closure cap may possibly fracture or break....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Kentec Medical, Inc

Recalled Item: Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes....

The Issue: Feeding tube plastic tethered closure cap may possibly fracture or break....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Kentec Medical, Inc

Recalled Item: Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes....

The Issue: Feeding tube plastic tethered closure cap may possibly fracture or break....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Kentec Medical, Inc

Recalled Item: Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes....

The Issue: Feeding tube plastic tethered closure cap may possibly fracture or break....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Kentec Medical, Inc

Recalled Item: Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes....

The Issue: Feeding tube plastic tethered closure cap may possibly fracture or break....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Beckman Coulter Inc.

Recalled Item: LabPro Data Management System Recalled by Beckman Coulter Inc. Due to A...

The Issue: A security-only update was released via remote diagnostics on January 14,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Ormco/Sybronendo

Recalled Item: SnapLink Recalled by Ormco/Sybronendo Due to The action is being taken due...

The Issue: The action is being taken due to an increase in complaints relating to the...

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

Class II — Potential Health HazardOngoing