State
72,984 recalls have nationwide distribution and so reach Georgia. 9,588 additional recalls listed Georgia specifically in their distribution scope.
Of the 9,588 recalls naming Georgia we have scored against our rubric, 1,464 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,164 (23%) are Severe.
Which agencies issued them
These figures cover only the 9,588 recalls whose distribution notice names Georgia specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Zenshi Handcrafted Sushi Happy Heart Platter #2 is being recalled over cucumbers recalled for possible Salmonella. 2,609 trays are affected.
Harris Teeter is recalling ZENSHI Handcrafted Sushi Hawaiian Roll products because the cucumbers used in production were recalled due to possible Salmonella contamination.
Zenshi Handcrafted Sushi Cream Cheese Roll with salmon is being recalled over cucumbers recalled for possible Salmonella. 5,350 trays are affected.
Zicam Nasal AllClear swabs are being recalled because of fungal contamination of the nasal swabs. All lots are affected, covering 13,632 cartons.
Zenshi Handcrafted Sushi Hawaiian Roll is being recalled because it was made with cucumbers recalled over possible Salmonella. 1,269 trays are affected.
Sandoz Cefazolin for Injection 1 gram is being recalled after cartons were found to contain vials labeled as penicillin G potassium. 208,300 vials are affected.
Harris Teeter is recalling ZENSHI Handcrafted Sushi Happy Heart Platter #3 (Crunchy Dragon Tempura) because recalled cucumbers used in the product may contain Salmonella.
Zenshi Handcrafted Sushi Hybrid Ni Platter is being recalled because it was made with cucumbers recalled over possible Salmonella. 7 trays are affected.
Zenshi Handcrafted Sushi Yuzu Teriyaki Sauce is being recalled because it was made with cucumbers recalled over possible Salmonella. 39 trays are affected.
The Philips Respironics BiPAP V30 Auto Ventilator is being recalled because the device does not indicate for use in patients with respiratory failure. 5,958 units affected.
Philips Ultrasound, Inc is recalling 5,230 Philips 3D9-3v Transducer devices because they were refurbished beyond their useful life, posing a risk of device failure during medical use.
Zenshi Handcrafted Sushi Ultimate Chili Roll with tuna is being recalled over cucumbers recalled for possible Salmonella. 1,365 trays are affected.
Harris Teeter is recalling ZENSHI HANDCRAFTED SUSHI Crunchy CA Roll (Brown Rice) due to possible Salmonella contamination from recalled cucumbers used in the product.
Tailstorm Health Inc. is recalling bupivacaine HCL sterile injection vials nationwide due to FDA inspection findings regarding concerns with the sterile manufacturing process.
Zenshi Handcrafted Sushi California Salad Roll is being recalled over cucumbers recalled for possible Salmonella. 2,883 trays are affected.
Hardy Diagnostics is recalling HardyCHROM CRE culture medium (Catalog No. G323) distributed across 22 US states and Puerto Rico. The product failed quality control testing due to breakthrough growth of Klebsiella pneumoniae.
Zicam Cold Remedy Medicated Nasal Swabs are being recalled because of fungal contamination of the swabs. All lots are affected, covering 3,374,918 cartons.
Zenshi Handcrafted Sushi Spicy California Roll is being recalled because it was made with cucumbers recalled over possible Salmonella. 30,174 trays are affected.
Zenshi Handcrafted Sushi Mango Red Rock is being recalled because it was made with cucumbers recalled over possible Salmonella. 184 trays are affected.
Servo-u MR Ventilator System (Model 6888800) may measure patient circuit compliance inaccurately due to incorrect pre-use leakage testing and incorrect active humidifier use.
Harris Teeter is recalling ZENSHI HANDCRAFTED SUSHI Crunchy Roll - Salmon products due to possible Salmonella contamination from recalled cucumbers used in production.
C.R. Bard Inc is recalling 63 units of the Bard Urologist's Tray due to cather packaging that may contain the incorrect French size, which could affect device use.
Philips Ultrasound, Inc. is recalling Philips C9-5EC transducer devices that were refurbished beyond their useful life, which may affect device performance and safety.
Apex Knee System components are being recalled because the age of the nylon packaging material has caused a loss of integrity of some pouches. 341 units are affected.
Medline Industries is recalling specific Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters because the needle may be slow to retract or fail to retract during catheter insertion.