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. 2,550 recalls have been distributed to Georgia in the last 12 months.
Showing 46521–46540 of 53,623 recalls
Recalled Item: Candied pecans: milk chocolate Recalled by Pecan Shed Due to Undeclared Soy
The Issue: Presence of undeclared soy allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Candied pecans: creamy white Recalled by Pecan Shed Due to Undeclared Soy
The Issue: Presence of undeclared soy allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Divinity with Pecans Fudge Recalled by Pecan Shed Due to Undeclared Allergens
The Issue: Presence of undeclared allergens soy, milk & pecans
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Butter Pecan Fudge Recalled by Pecan Shed Due to Undeclared Allergens
The Issue: Presence of undeclared allergens soy, milk, and pecans
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pumpkin Pie with Pecans Fudge Recalled by Pecan Shed Due to Undeclared Allergens
The Issue: Presence of undeclared allergens soy, milk, and pecans
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Candied pecans: dark chocolate Recalled by Pecan Shed Due to Undeclared Soy
The Issue: Presence of undeclared soy allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ExtenZe 600 mg Recalled by Schindele Enterprises dba Midwest Wholesale Due...
The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heparin Sodium 2000 USP Heparin Units per 1000 mL (2 Recalled by Hospira...
The Issue: Lack of Assurance of Sterility; potential leakage from administrative port.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SEXY MONKEY Recalled by Schindele Enterprises dba Midwest Wholesale Due to...
The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: XZONE GOLD Recalled by Schindele Enterprises dba Midwest Wholesale Due to...
The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Magic For Men Recalled by Schindele Enterprises dba Midwest Wholesale Due to...
The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BOOST ULTRA Recalled by Schindele Enterprises dba Midwest Wholesale Due to...
The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: XZEN PLATINUM Recalled by Schindele Enterprises dba Midwest Wholesale Due to...
The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MiracleZEN Platinum Recalled by Schindele Enterprises dba Midwest Wholesale...
The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aminosyn 3.5% M Sulfite-Free Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility; potential leakage from administrative port.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Smith & Nephew RENASYS Soft Port (The RENASYS Recalled by Smith & Nephew...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS-F XL with Soft Port REF #: Recalled by Smith & Nephew...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS-F Foam Dressing Kit with Soft Port REF #'s: 66800794...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Model 7305- Mosaic Aortic Obturator The Mosaic Aortic Recalled...
The Issue: Medtronic, Inc. initiated a recall of Medtronic Mosaic Aortic Obturator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products White Slides Recalled by Ortho-Clinical...
The Issue: An incorrect assay value (0.3785) was printed on the product carton for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.