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. 999 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
999 in last 12 months

Showing 38301–38320 of 53,829 recalls

Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548470 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: MM00548410 (XMD Recalled...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548680 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548950 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548650 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548830 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549570 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548850 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549390 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548560 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548750 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548920 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· MOOG Medical Devices Group

Recalled Item: Moog Curlin Infusion Recalled by MOOG Medical Devices Group Due to Moog is...

The Issue: Moog is recalling Curlin 4000, 6000, and PainSmart Infusion Pumps...

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

Class II — Potential Health HazardOngoing
FoodDecember 23, 2015· Milky Way Intl Trading Corp

Recalled Item: Mandarin Oranges (In Light Syrup) Recalled by Milky Way Intl Trading Corp...

The Issue: MW Polar Foods is recalling Mandarin Oranges due to possible glass in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 23, 2015· Nuway Distributors, LLC

Recalled Item: APEXXX tablets Recalled by Nuway Distributors, LLC Due to Marketed Without...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 22, 2015· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2015· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2015· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2015· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2015· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...

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

Class II — Potential Health HazardOngoing
Refund