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. 1,003 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
1,003 in last 12 months

Showing 42721–42740 of 53,623 recalls

Medical DeviceJanuary 21, 2015· Merge Healthcare, Inc.

Recalled Item: Merge Hemo Recalled by Merge Healthcare, Inc. Due to A system freeze-up of...

The Issue: A system freeze-up of the Merge Hemo system, that included the PHASEIN End...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2015· iCAD, Inc.

Recalled Item: DynaLOC Breast Interventional Planning Software Versions 3.1 and 3.2...

The Issue: A device malfunction may cause the biopsy needle to fail to reach the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2015· TeraRecon, Inc.

Recalled Item: Aquarius iNtuition Client Viewer. Findings Workflow module Recalled by...

The Issue: Software anomaly related to RECIST1.1 target lesion evaluation criteria in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens LANTIS Oncology Information System Servers Recalled by Siemens...

The Issue: There is a potential safety risk when using LANTIS server software with...

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

Class II — Potential Health HazardOngoing
DrugJanuary 21, 2015· Sun Pharma Global Fze

Recalled Item: Levetiracetam Recalled by Sun Pharma Global Fze Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications: 6 month time point.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 21, 2015· Sun Pharma Global Fze

Recalled Item: Ketorolac Tromethamine Ophthalmic Solution Recalled by Sun Pharma Global Fze...

The Issue: Presence of Particulate Matter: lot is not meeting the specification limit...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 20, 2015· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter; Hospira has identified the particulate as a...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 20, 2015· Pacifico National, Inc. dba AmEx Pharmacy

Recalled Item: Avastin (Bevacizumab) 1.25 mg/0.05 mL syringe Recalled by Pacifico National,...

The Issue: Non-Sterility: Product tested positive for bacterial contamination.

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 20, 2015· Pacifico National, Inc. dba AmEx Pharmacy

Recalled Item: Avastin (Bevacizumab) 2 mg/0.08 mL syringe Recalled by Pacifico National,...

The Issue: Non-Sterility: Product tested positive for bacterial contamination.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 19, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Systems Drug Calibrator I Recalled by Siemens Healthcare...

The Issue: Incorrect calibrator lot values were assigned for ADVIA Chemistry Systems...

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

Class II — Potential Health HazardOngoing
FoodJanuary 19, 2015· Ungar's Food Products, Inc.

Recalled Item: Dr. Praeger's Sensible Foods Bombay Curry Veggie Burgers 11 oz Recalled by...

The Issue: Ungar's Food Products Inc. was notified by a supplier that cumin, an...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 16, 2015· Aron Streit Inc.

Recalled Item: Streit's Kids Dark CHOCOLATE Coins Recalled by Aron Streit Inc. Due to...

The Issue: State of New York Department of Agriculture and Markets tested revealed...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 16, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Artis One Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The possibility exists that the monitor may fail and requires a power circle...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2015· HeartWare Inc

Recalled Item: HeartWare Ventricular Assist System (HeartWare Controller) Product Usage:...

The Issue: The affected clinical trial Controllers exhibit a higher susceptibility to...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 16, 2015· CME America, LLC

Recalled Item: BodyGuard 323 pump Recalled by CME America, LLC Due to CME America is...

The Issue: CME America is recalling the BodyGuard and BodyGuard 323 Infusion pumps due...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2015· Brainlab AG

Recalled Item: The Brainlab Offset Cup Impactor Universal. Part of the Brainlab Recalled by...

The Issue: The recommended sterilization and drying parameters are not effective to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2015· Invacare Corporation

Recalled Item: TDX Electric Wheelchair. Invacare FDX Recalled by Invacare Corporation Due...

The Issue: If the slack in the wires is not routed and secured correctly, flexing of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2015· Intuitive Surgical, Inc.

Recalled Item: da Vinci Si Surgical System Recalled by Intuitive Surgical, Inc. Due to The...

The Issue: The Wall chart has been updated because it was noted that Wall Chart (PN...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2015· Churchill Medical Systems, Inc.

Recalled Item: 4" Trifurcated set with Bionectors and check valves Recalled by Churchill...

The Issue: Potential for leaking caused by insufficient bond between needleless device...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2015· Churchill Medical Systems, Inc.

Recalled Item: 4" Microbore T-Port Set Recalled by Churchill Medical Systems, Inc. Due to...

The Issue: Potential for leaking caused by insufficient bond between needleless device...

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

Class II — Potential Health HazardOngoing