State
73,738 recalls have nationwide distribution and so reach Georgia. 9,632 additional recalls listed Georgia specifically in their distribution scope.
Of the 9,632 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 2,565 (27%) are Severe.
Which agencies issued them
These figures cover only the 9,632 recalls whose distribution notice names Georgia specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Skacel Collection is recalling US 6 (4.0mm) addi® FlipStix knitting needles because the aluminum shafts can split or burst, posing a laceration hazard.
GE Healthcare is recalling 43 CardioLab/ComboLab Recording Systems because a failure in connected devices could cause electrical shock to patients.
Blue Bird is recalling 2013-2020 Vision school buses with Ford engines because brake lights may stay on continuously, increasing crash risk.
Valeritas is recalling 60 DEMO No Needle Corrugated Cartons because they may contain a needle. The units were distributed nationwide in the U.S.
Valeritas is recalling DEMO No Needle Corrugated Cartons because there is a potential for the units to contain a needle.
Valeritas is recalling 852 DEMO No Needle Corrugated Cartons because they may contain a needle. The units were distributed nationwide in the U.S.
Baxter Healthcare is recalling 504 TherMax Blood Warmer Units because they may not meet electrical safety standards for protective earth connections.
Stryker Neurovascular is recalling 831 units of Synchro2 Soft Guidewires due to a potential loss of sterility. The recall covers units distributed worldwide.
Blue Bird is recalling 2013-2020 Vision transit buses with Ford engines because a defective brake light switch bracket may cause brake lights to stay on, increasing crash risk.
Valeritas is recalling 21,714 DEMO No Needle Corrugated Cartons because they may contain a needle. The recall covers units distributed nationwide in the U.S.
Pajunk GmbH is recalling Sprotte Lumbar Puncture Needles because a packaging sealing issue may affect sterility. The recall covers 40,475 devices distributed worldwide.
LivaNova USA Inc. is recalling SORIN Heater-Cooler System 3T units because a chemical reaction may render the water preservative ineffective, potentially allowing micro-organism growth.
Senseonics is recalling 1,344 Eversense CGM sensors nationwide because they may stop working early due to inadequate hydration of the glucose-sensing surface.
Glenmark Pharmaceuticals is recalling Estradiol Vaginal Inserts because the applicator plunger may be difficult to push.
Stryker Neurovascular is recalling Synchro2 guidewires because the product labels contain a typographical error in the millimeter dimension for the outer diameter.
Alto Development Corp is recalling 209 Thorecon Plating System Kits because a molding defect renders the disposable tensioners inoperable.
Blue Bell Creameries is recalling specific lots of Butter Crunch Ice Cream due to possible foreign material in the product.
Mindray is recalling 13 Accutorr 3 Vital Signs Monitors because the NIBP valve assembly board contains software features not included in the current marketing clearance.
Stryker Neurovascular is recalling 305 Synchro2 guidewires because the product labels contain a typographical error in the millimeter dimension.
Taro Pharmaceuticals is recalling 5,280 bottles of Children's Ibuprofen Oral Suspension due to the presence of small inert plastic particles.
Alto Development Corp is recalling 209 Thorecon Plating System Kits because a molding defect renders the disposable tensioners inoperable.
Labstyle Innovations is recalling the Dario Blood Glucose Monitoring System Android app versions 4.3.0-4.3.2 because it may duplicate blood glucose readings.
Stryker Neurovascular is recalling 107 Synchro2 guidewires because the product labels contain a typographical error in the millimeter dimension for the outer diameter.
Alto Development Corp is recalling 209 Thorecon Plating System Kits because a molding defect renders the tensioners inoperable.
Implant Direct is recalling 107 Scan Adapter Assemblies due to incorrect assembly that may prevent clinicians from capturing implant positions, causing patient delays.