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. 2,643 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,643 in last 12 months

Showing 3046130480 of 53,623 recalls

Medical DeviceJuly 4, 2017· Stanmore Implants Worldwide Ltd.

Recalled Item: JTS External Drive Unit JTS Distal Femoral Extendible Implant Femur Recalled...

The Issue: Three (3) complaints were identified in which the potential for utilization...

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

Class II — Potential Health HazardOngoing
FoodJuly 3, 2017· The Kroger Co

Recalled Item: Comforts FOR BABY Purified Water with Flouride Added. 1 GAL Recalled by The...

The Issue: the firm received a complaint of mold found in the product.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 30, 2017· Sorin Group USA, Inc.

Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...

The Issue: Plastic heat exchanger fibers separating the blood compartment from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Sorin Group USA, Inc.

Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...

The Issue: Plastic heat exchanger fibers separating the blood compartment from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Sorin Group USA, Inc.

Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...

The Issue: Plastic heat exchanger fibers separating the blood compartment from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Sorin Group USA, Inc.

Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...

The Issue: Plastic heat exchanger fibers separating the blood compartment from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Alcon Research, Ltd.

Recalled Item: ORA System with VerifEye Recalled by Alcon Research, Ltd. Due to Some ORA...

The Issue: Some ORA Carts have the potential to return an incorrect IOL power...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Sorin Group USA, Inc.

Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...

The Issue: Plastic heat exchanger fibers separating the blood compartment from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Sorin Group USA, Inc.

Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...

The Issue: Plastic heat exchanger fibers separating the blood compartment from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Elekta, Inc.

Recalled Item: MOSAIQ Medical Charged-Particle Radiation Therapy System Recalled by Elekta,...

The Issue: The table shift in the vertical direction was inverted during the use of CMA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Alcon Research, Ltd.

Recalled Item: ORA System with VerifEye+ Cart Recalled by Alcon Research, Ltd. Due to Some...

The Issue: Some ORA Carts have the potential to return an incorrect IOL power...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· R82 A/S

Recalled Item: Heron toilet and bath chair Model 880505-01 & 880505-11 Recalled by R82 A/S...

The Issue: Replacement campaign on all units that have a gas spring head in aluminum.

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

Class II — Potential Health HazardOngoing
DrugJune 29, 2017· Teva Pharmaceuticals USA

Recalled Item: Buprenorphine and Naloxone Sublingual Tablets Recalled by Teva...

The Issue: Failed Impurities/Degradation Specifications: out of specification test...

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

Class III — Low RiskOngoing
Refund
DrugJune 29, 2017· Teva Pharmaceuticals USA

Recalled Item: Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg 30 tablets per...

The Issue: Failed Impurities/Degradation Specifications: out of specification test...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 29, 2017· Boston Scientific Corporation

Recalled Item: EMBLEM MRI S-ICD Model 219 Recalled by Boston Scientific Corporation Due to...

The Issue: The device can deliver an atypical amount of energy due to memory corruption...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Roche Diagnostics Corporation

Recalled Item: Brand Name: ¿ cobas c 6000 MODULAR Series System e Recalled by Roche...

The Issue: Roche has confirmed that a possible sample mismatch issue may occur on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: STERILE SAMPLE SORIN GROUP Recalled by Sorin Group USA, Inc. Due to...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing