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. 1,076 recalls have been distributed to Georgia in the last 12 months.
Showing 21021–21040 of 53,623 recalls
Recalled Item: Ketorolac Tromethamine Injection Recalled by Hikma Pharmaceuticals USA Inc....
The Issue: Presence of Particulate Matter: particles identified as polydimethylsiloxane...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Injection Recalled by Hikma Pharmaceuticals USA Inc....
The Issue: Presence of Particulate Matter: particles identified as polydimethylsiloxane...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GREY GHOST BAKERY scratch-made cookies LEMON SUGAR NET WT 1.4 OZ (40 G)...
The Issue: The product contains undeclared sulfites.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 16MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer 6.0 Recalled by GE Healthcare, LLC Due to...
The Issue: Centricity Universal Viewer measurements saved into a DICOM Grayscale...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stratum Lapidus Plate - Small Rt Recalled by Nextremity Solutions Due to The...
The Issue: The product contains a different plate than indicated by the package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 12MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 10MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbiologics QC Sets and Panels Recalled by Microbiologics Inc Due to The...
The Issue: The recommended hydration fluid for the 8180 Gram-Positive Blood Culture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 18MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 2- IVD calibrator for VITROS...
The Issue: Potential for Negatively Biased Na+ Urine Results Using Several Lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 24MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NORepinephrine Bitartrate 8 mg added to 250 mL 5% Dextrose Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine Bitartrate 4 mg added to 250 mL 5% Dextrose Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrocortisone and Acetic Acid Otic Solution Recalled by Akorn Inc Due to...
The Issue: Subpotent Drug: Low Out of specification (OOS) assay results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine Bitartrate 8 mg added to 500 mL 5% Dextrose Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HOME CHEF HEAT & EAT Baked Macaroni & Cheese NET Recalled by Bakkavor Foods...
The Issue: The firm received a complaint from one of their customers that the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Plant Based WayFare Chocolate Pudding Organic Dairy Free Recalled by Wayfare...
The Issue: Product recalled due to consumer complaints for bloating of package, off...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Plant Based WayFare Vanilla Pudding Organic Dairy Free Recalled by Wayfare...
The Issue: Product recalled due to consumer complaints for bloating of package, off...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Plant Based WayFare Butterscotch Pudding Organic Dairy Free Recalled by...
The Issue: Product is recalled due to consumer complaints for bloating of package, off...
Recommended Action: Do not consume. Return to store for a refund or discard.