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. 2,630 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,630 in last 12 months

Showing 3376133780 of 53,623 recalls

FoodDecember 7, 2016· Publix Super Markets, Inc.

Recalled Item: Publix Premium Pumpkin Pancake & Waffle Mix Recalled by Publix Super...

The Issue: Milk powder used as ingredient may contain Salmonella.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 7, 2016· Cardiovascular Systems Inc

Recalled Item: DIAMONDBACK 360 Peripheral 1.50 Classic Recalled by Cardiovascular Systems...

The Issue: CSI discovered that a 1.50mm Solid Crown OAD was labeled as a 1.50mm Crown OED.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2016· Stanmore Implants Worldwide Ltd.

Recalled Item: Femoral Shaft L=120mm Recalled by Stanmore Implants Worldwide Ltd. Due to...

The Issue: The recalling firm has received 5 customer inquiries reporting that at least...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2016· Stanmore Implants Worldwide Ltd.

Recalled Item: DF Coated Integral Shaft & Stem 15x30x38 Recalled by Stanmore Implants...

The Issue: The recalling firm has received 5 customer inquiries reporting that at least...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2016· Stanmore Implants Worldwide Ltd.

Recalled Item: Tibial Component Metal Cased Small Long Recalled by Stanmore Implants...

The Issue: The recalling firm has received 5 customer inquiries reporting that at least...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2016· Stanmore Implants Worldwide Ltd.

Recalled Item: Femoral Integral Shaft & Stem 15x27 HA Coated Recalled by Stanmore Implants...

The Issue: The recalling firm has received 5 customer inquiries reporting that at least...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2016· Medacta Usa Inc

Recalled Item: Medacta International SA Recalled by Medacta Usa Inc Due to Damaged...

The Issue: Damaged packaging, lack of sterility assurance

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2016· Stanmore Implants Worldwide Ltd.

Recalled Item: Tibial Component Fixed Hinge Small Long Recalled by Stanmore Implants...

The Issue: The recalling firm has received 5 customer inquiries reporting that at least...

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

Class II — Potential Health HazardOngoing
DrugDecember 7, 2016· Novum Pharma, LLC

Recalled Item: Novacort Gel Sample Packets (2% hydrocortisone acetate Recalled by Novum...

The Issue: Subpotent Drug: Out of specification result for pramoxine hydrochloride

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 6, 2016· Stryker Sustainability Solutions

Recalled Item: Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT Recalled by...

The Issue: A breach in the sterile packaging may have occurred resulting in potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2016· Stryker Sustainability Solutions

Recalled Item: Reprocessed Electrophysiology Catheter Cables Catalog Number: CB3434CT...

The Issue: A breach in the sterile packaging may have occurred resulting in potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· BARD PERIPHERAL VASCULAR, INC

Recalled Item: Halo One 5F Introducer Sheath 90 cm Product Code: HAL590 Recalled by BARD...

The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 2, 2016· BARD PERIPHERAL VASCULAR, INC

Recalled Item: Halo One 5F Introducer Sheath 45 cm Product Code: HAL545 Recalled by BARD...

The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 2, 2016· Elekta, Inc.

Recalled Item: MOSAIQ Oncology Information System The product is used to manage Recalled by...

The Issue: Edits to Particle field definition parameters may not be saved when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Reunion TSA Peg Alignment Sound Catalog #5901-1038 The Peg Alignment...

The Issue: Reunion TSA Peg Alignment Sound broke during surgery.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· CareFusion 303, Inc.

Recalled Item: Alaris Pump Module Recalled by CareFusion 303, Inc. Due to During an...

The Issue: During an infusion, a false Air-in-Line (AIL) alarm would cause the infusion...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 2, 2016· BARD PERIPHERAL VASCULAR, INC

Recalled Item: Halo One 5F Introducer Sheath 10 cm 5 pack Product Recalled by BARD...

The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.

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

Class I — Serious Health HazardOngoing
FoodDecember 2, 2016· Phil-Am Trading, Inc.

Recalled Item: Phil-Am Smoked Mackerel (Hasa Hasa) Net. Wt. 200g (7.05 oz.) Recalled by...

The Issue: Phil-am Trading, Inc. is recalling Phil-am Smoked Mackerel (Hasa-Hasa),...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 2, 2016· K2M, Inc

Recalled Item: K2M Special Connector Instruments (Special Connector Recalled by K2M, Inc...

The Issue: Instruments were developed without adequate consideration given to the need...

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

Class II — Potential Health HazardOngoing
DrugDecember 2, 2016· Shire PLC

Recalled Item: Pentasa (mesalamine) Controlled-Release Capsules Recalled by Shire PLC Due...

The Issue: Presence of Foreign Tablets/Capsules; 500 mg capsules were found in bottles...

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

Class III — Low RiskOngoing
Refund