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. 1,955 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
1,955 in last 12 months

Showing 2578125800 of 53,623 recalls

Medical DeviceSeptember 28, 2018· TriMed Inc.

Recalled Item: TriMed Wrist Hook Dorsal Impactor Recalled by TriMed Inc. Due to The WHD/WHV...

The Issue: The WHD/WHV impactors can rust over time due to an improper manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· Tosoh Bioscience Inc

Recalled Item: AIA-2000 Analyzer Recalled by Tosoh Bioscience Inc Due to Tosoh Bioscience...

The Issue: Tosoh Bioscience has become aware of a potential issue with the AIA-900 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· Tosoh Bioscience Inc

Recalled Item: AIA-900Analyzer Recalled by Tosoh Bioscience Inc Due to Tosoh Bioscience has...

The Issue: Tosoh Bioscience has become aware of a potential issue with the AIA-900 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· Tosoh Bioscience Inc

Recalled Item: AIA-2000 Analyzer Recalled by Tosoh Bioscience Inc Due to There is a...

The Issue: There is a possibility that the liquid suction pump on some AIA-2000...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· Tosoh Bioscience Inc

Recalled Item: Tosoh AIA-900 immunoassay Analyzer Recalled by Tosoh Bioscience Inc Due to A...

The Issue: A software issue may cause the liquid volume detection entries for 2nd and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Thermal Chamber Motor Cable located in the following models:...

The Issue: Thermal chamber motors have electrical cables with single insulation rather...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· Siemens Medical Solutions USA, Inc.

Recalled Item: Biograph mCT: a) S(64)-3R Recalled by Siemens Medical Solutions USA, Inc....

The Issue: The terminals on the plug may become loose and overheat.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· Siemens Medical Solutions USA, Inc.

Recalled Item: Biograph Horizon a) 3R Recalled by Siemens Medical Solutions USA, Inc. Due...

The Issue: The terminals on the plug may become loose and overheat.

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

Class II — Potential Health HazardOngoing
FoodSeptember 27, 2018· Aldi Inc

Recalled Item: Millville Maple & Brown Sugar Instant Oatmeal 15.1 oz. 10 Recalled by Aldi...

The Issue: Complaints of insects in product

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing