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. 2,831 recalls have been distributed to Georgia in the last 12 months.
Showing 6141–6160 of 53,623 recalls
Recalled Item: Grande Lactose SKU 30600. Grade A. Pasteurized. Net Wt Recalled by GRANDE...
The Issue: Possible Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Grande Grande Primo Y45 Cultured Dairy Product. Product Code: 32400....
The Issue: Possible Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Grande Bravo 600 Functional Whey Protein SKU 32106. 34% Protein. Recalled by...
The Issue: Possible Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Grande Bravo 500 Functional Whey Protein SKU 32103. 34% Protein. Recalled by...
The Issue: Possible Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Grande Ultra 9150 Whey Protein Isolate. Product Code: 32324. 90% Recalled by...
The Issue: Possible Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sirolimus Tablets 1mg Tablets 100-count bottle Recalled by Dr. Reddy's...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Meijer Magnesium Citrate Saline Laxative Oral Solution Dye Free Recalled by...
The Issue: Microbial Contamination of Non-Sterile Products - Presence of Acetobacter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CVS Health Magnesium Citrate Saline Laxative Oral Solution DYE FREE Recalled...
The Issue: Microbial Contamination of Non-Sterile Products - Presence of Acetobacter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The D*Clot¿ HD Rotational Thrombectomy System is a percutaneous...
The Issue: Internal product testing failed bubble leak testing (ASTM F2096), which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardura XL (doxazosin) extended release tablets 8mg Recalled by Viatris Inc...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardura XL (doxazosin) extended release tablets 4mg Recalled by Viatris Inc...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl 1000mcg/100mL (10mcg/mL) in 0.9% Sodium Chloride Injection Recalled...
The Issue: Labeling: Wrong Barcode
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZOLL 731 Ventilator (EMV+ Recalled by ZOLL Medical Corporation Due to...
The Issue: Operator's Guide & Quick Guide (QRG) ZOLL 731 Ventilator for MRI Compatible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TabloCart with Prefiltration Drawer PN-0006813 Recalled by Outset Medical,...
The Issue: A cart with prefiltration drawer, an optional hemodialysis system accessory,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE STERILE IRIS SCISSORS CVD/STD (case) and DYNJ04049H Recalled by...
The Issue: There is the potential of the tip protector to fall off 4.5" sterile,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phenylephrine in 0.9% Sodium Chloride Injection Preservative Free Recalled...
The Issue: Labeling: Label mix-up - ephedrine syringes mislabeled as phenylephrine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Decompression Table Model E9011. This device applies cervical and/or lumbar...
The Issue: This product is being recalled due to potentially insufficient rework on a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.