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. 2,793 recalls have been distributed to Georgia in the last 12 months.
Showing 11741–11760 of 53,623 recalls
Recalled Item: Budesonide Inhalation Suspension 0.25mg/2mL Recalled by CIPLA Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: B. Braun CARESITE Port Access Kit w/Tegaderm Recalled by Medical Action...
The Issue: The kits were incorrectly labeled with an extended expiration date of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESITE SMALLBORE EXT SET T-PORT 5 IN. Recalled by B. Braun Medical, Inc....
The Issue: The extension set has a high probability of potential failure which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTRASITE US04TL Smallbore T-Port Extension Set Recalled by B. Braun...
The Issue: The extension set has a high probability of failure which could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Tube Sodium Fluoride: 100 mg Recalled by Becton Dickinson &...
The Issue: The affected product contains isobutylene which has recently demonstrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extension Set Recalled by B. Braun Medical, Inc. Due to The extension set...
The Issue: The extension set has a high probability of failure which could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phytonadione Injectable Emulsion USP Recalled by Dr. Reddy's Laboratories,...
The Issue: Failed Stability Specifications: Out of specification results reported at...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ARIES SARS-CoV-2 Assay Recalled by Luminex Corporation Due to A part defect...
The Issue: A part defect with the wash 1 syringe of an SARS-CoV-2 assay could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW Pressure Injectable Arrowg+ard Blue Advance Two-Lumen Midline Kit...
The Issue: Mislabeling: the corrugate label, lidstock, banner card, and peel sticker...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex HF20 Set (product code 109841). For use in providing Recalled by...
The Issue: Within the current Prismaflex set IFU (instructions for use), there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex ST Set: ST60 (product code 107643) Recalled by Baxter Healthcare...
The Issue: Within the current Prismaflex set IFU (instructions for use), there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex M Set: M60 (product code 106696) Recalled by Baxter Healthcare...
The Issue: Within the current Prismaflex set IFU (instructions for use), there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex M Set: M150 (product code 109990). For use in Recalled by Baxter...
The Issue: Within the current Prismaflex set IFU (instructions for use), there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex HF Set: HF1000 (product code 107140) Recalled by Baxter...
The Issue: Within the current Prismaflex set IFU (instructions for use), there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lisinopril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to Foreign...
The Issue: Presence of Foreign Substance: Foreign material (metal piece) embedded in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NovoTHOR Gen 2.5 Regular whole body red light therapy bed Recalled by Thor...
The Issue: Failure of ball stud components causing the gas strut on one side to detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovoTHOR Gen 2.0 whole body red light therapy bed Recalled by Thor...
The Issue: Failure of ball stud components causing the gas strut on one side to detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G041 POD Recalled by Thor Photomedicine Ltd Due to Failure of ball stud...
The Issue: Failure of ball stud components causing the gas strut on one side to detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovoTHOR Gen 2.5 XL whole body red light therapy bed Recalled by Thor...
The Issue: Failure of ball stud components causing the gas strut on one side to detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triamcinolone Acetonide cream Recalled by Direct Rx Due to CGMP Deviations:...
The Issue: CGMP Deviations: Product complaints reporting the product to have a gritty...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.