State
73,827 recalls have nationwide distribution and so reach Georgia. 9,635 additional recalls listed Georgia specifically in their distribution scope.
Of the 9,635 recalls naming Georgia we have scored against our rubric, 1,471 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,567 (27%) are Severe.
Which agencies issued them
These figures cover only the 9,635 recalls whose distribution notice names Georgia specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Rabbit Creek Products Inc. is recalling Creme Brulee Brownie Mix because the flour used may have been contaminated with E. coli O121.
Ducati is recalling 2016-2017 XDiavel motorcycles because a loose side stand screw may cause the bike to fall or the engine to stall.
Rabbit Creek Products Inc. is recalling Cappuccino with Chocolate Chips Muffin Mix because the flour used may be contaminated with E. coli O121.
Rabbit Creek Products is recalling Buffalo Wing Beer Bread Mix because the flour used may have been contaminated with E. coli O121.
Rabbit Creek Products Inc. is recalling Paddy's Pub Classic Beer Bread Mix because it may contain flour contaminated with E. coli O121.
Rabbit Creek Products Inc. is recalling Million Dollar Brownie Mix because it may contain flour contaminated with E. coli O121. Consumers should stop using the product.
Rabbit Creek Products is recalling Flower Pot Parmesan Southwest Beer Bread Mix because it may contain flour contaminated with E. coli O121.
Rabbit Creek Products Inc. is recalling Caramel Pecan with Streusel Topping Quick Bread Mix because it may contain flour contaminated with E. coli O121.
Rabbit Creek Products Inc. is recalling Raspberry with Cabernet Wine Brownie Mix because it may contain flour contaminated with E. coli O121.
Rabbit Creek Products is recalling Redneck Brownie Mix because it may contain flour contaminated with E. coli O121.
Siemens is recalling 37 Ysio Max radiographic systems because a table part may detach, causing the table to tilt and potentially injure patients.
Ford is recalling 2017 Lincoln Continental vehicles because incorrect headlight lenses may reduce turn signal visibility, increasing crash risk.
Integra LifeSciences Corp. is recalling specific lots of Integra Drainage Accessory Kits because a final inspection found an incomplete packaging seal, potentially compromising sterility.
Trumpf Medical Systems is recalling 84 Stationary Column TruSystem 7599 units because they may unexpectedly descend approximately 20 centimeters.
Trumpf Medical Systems is recalling 84 TruSystem 7000 U operating tables because they may unexpectedly descend approximately 20 centimeters.
Trumpf Medical Systems is recalling 84 Floor Mounting Columns because they unexpectedly descended approximately 20 centimeters, posing a risk to patient safety during surgery.
Forest River is recalling 2016-2017 Coachmen Galleria recreational vehicles because the cargo capacity placard is inaccurate, which may lead to overloading.
ShowHauler is recalling 2014-2015 Garage Coaches because lift gate roller chains may fail, causing the platform to drop and increasing injury risk.
Siemens is recalling 37 Multix Fusion X-ray systems because an internal table part may detach, causing the table to tilt and potentially injure patients.
RaySearch is recalling RayStation software versions 2.5 through 5.0 due to dose calculation errors when using specific region of interest settings.
Integra LifeSciences Corp. is recalling 10 units of Straight Ventricular Catheters due to an incomplete packaging seal discovered during final inspection.
Integra LifeSciences Corp. is recalling 14 units of the Ventricular Catheter Accessory Kit due to an incomplete sterile packaging seal discovered during final inspection.
Siemens Healthcare Diagnostics is recalling Dimension Vista Calcium reagent cartridges that may produce inaccurate test results.
Siemens is recalling 37 Multix Fusion VA10 radiographic systems because a table part may detach, causing the table to tilt and potentially injure patients.
Microgenics Corporation is recalling the Thermo Scientific QMS Everolimus Assay because a reagent stability issue causes inaccurate test results for transplant patients.