Product Recalls in Georgia

Product recalls affecting Georgia — including food, drugs, consumer products, medical devices, and vehicles distributed to Georgia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,819 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,819 in last 12 months

Showing 92219240 of 29,505 recalls

Medical DeviceAugust 25, 2021· Deerfield Imaging, Inc.

Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...

The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Atrium Medical Corporation

Recalled Item: Atrium ADVANTA VXT Vascular Graft Recalled by Atrium Medical Corporation Due...

The Issue: The product package may potentially contain a mismatched graft that does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Deerfield Imaging, Inc.

Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...

The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2021· Accelerated Care Plus Corporation

Recalled Item: Omnisound Gel Recalled by Accelerated Care Plus Corporation Due to...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 25, 2021· Deerfield Imaging, Inc.

Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...

The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Zhejiang Kindly Medical Devices Co., Ltd.

Recalled Item: HENRY SCHEIN Safety Blood Collection Needle 22Gx 1 1/4 Inch Recalled by...

The Issue: Potential for difficulty in safety mechanism activation.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Zhejiang Kindly Medical Devices Co., Ltd.

Recalled Item: HENRY SCHEIN Safety Blood Collection Needle 21Gx 1 1/4 Inch Recalled by...

The Issue: Potential for difficulty in safety mechanism activation.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Zhejiang Kindly Medical Devices Co., Ltd.

Recalled Item: McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder...

The Issue: Potential for difficulty in safety mechanism activation.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Zhejiang Kindly Medical Devices Co., Ltd.

Recalled Item: McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder...

The Issue: Potential for difficulty in safety mechanism activation.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Zhejiang Kindly Medical Devices Co., Ltd.

Recalled Item: McKesson PREVENT HT Safety Blood Collection Needles Recalled by Zhejiang...

The Issue: Potential for difficulty in safety mechanism activation.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Zhejiang Kindly Medical Devices Co., Ltd.

Recalled Item: McKesson PREVENT HT Safety Blood Collection Needles Recalled by Zhejiang...

The Issue: Potential for difficulty in safety mechanism activation.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Bard Peripheral Vascular Inc

Recalled Item: Catalog # BEK4511 Recalled by Bard Peripheral Vascular Inc Due to Due to...

The Issue: Due to misbranded products shipped to customers.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Bard Peripheral Vascular Inc

Recalled Item: Catalog # BEK3411 Recalled by Bard Peripheral Vascular Inc Due to Due to...

The Issue: Due to misbranded products shipped to customers.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· National Distribution & Contracting Inc

Recalled Item: ECO 50TS Gel Tens Ultrasound 1in X 5L cube 1 Dispenser Btl Recalled by...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 24, 2021· National Distribution & Contracting Inc

Recalled Item: ECO 85CB Lotion Ultrasound 8.5 oz 24/cs ECO 40JBC Gel Recalled by National...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 24, 2021· Medtronic Perfusion Systems

Recalled Item: DLP Left Heart Vent Catheters Recalled by Medtronic Perfusion Systems Due to...

The Issue: Potential for a wire protrusion through the left heart vent catheter tip

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Medtronic Perfusion Systems

Recalled Item: DLP Left Heart Vent Catheters Recalled by Medtronic Perfusion Systems Due to...

The Issue: Potential for a wire protrusion through the left heart vent catheter tip

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2021· Aesthetics Systems Usa Inc

Recalled Item: Action De Gala Recalled by Aesthetics Systems Usa Inc Due to Ultrasound gels...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 20, 2021· ConvaTec, Inc

Recalled Item: DuoDERM Control Gel Formula Border Dressings 15x15cm (1x5pk) Recalled by...

The Issue: Primary packaging labeling may be incorrect.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2021· Microbiologics Inc

Recalled Item: SARS-CoV-2 Process Control (Pellet) - Product Usage: intended for use...

The Issue: The SARS-CoV-2 Process Control (Pellet) contains RNA transcripts that...

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

Class II — Potential Health HazardOngoing