State

Georgia product recalls

73,806 recalls have nationwide distribution and so reach Georgia. 9,635 additional recalls listed Georgia specifically in their distribution scope.

What the numbers show

Total: 9,635
Critical: 1,471
Severe: 2,567
Most recent: 2026-11-04

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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41076–41100 of 83441

HighFDA (Devices)·Z-0364-2019·2018-11-07
Baxter Recalls Exactamix Empty EVA Bags Due to Leak Risk
Baxter Healthcare is recalling 110,134 units of Exactamix Empty EVA Bags because they may leak after being used for compounding sterile solutions.
Product
EXACTAMIX Empty EVA Bags - 500 mL - Product Usage: A plastic container used to hold large-volume sterile solutions to be administered to a patient through an intravascular administration set.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0111-2019·2018-11-07
Sprayology Recalls AllergEase Homeopathic Oral Spray Due to CGMP Deviations
Sprayology is recalling 4,153 bottles of AllergEase Homeopathic Oral Spray because manufacturing conditions could result in possible microbial contamination.
Product
AllergEase, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0003-1
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0306-2019·2018-11-07
Philips IQon Spectral CT Software Recall for Misleading Calcium Score Reports
Philips is recalling IQon Spectral CT scanners with specific software versions because the Calcium Score report provides confusing and potentially misleading plaque analysis data.
Product
IQon Spectral CT (Model No. 728332), Software Version 4.7.0 or 4.7.2 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0117-2019·2018-11-07
Sprayology Recalls Arnica Power Homeopathic Oral Spray Due to CGMP Deviations
Sprayology is recalling 3,531 bottles of Arnica Power Homeopathic Oral Spray due to manufacturing deviations that could result in microbial contamination.
Product
Arnica Power, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879.NDC 61096-0032-1
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0311-2019·2018-11-07
Philips Brilliance iCT SP CT Scanners Recalled for Misleading Calcium Score Reports
Philips is recalling 626 Brilliance iCT SP CT scanners because specific software versions generate confusing calcium score reports that may lead to patient mistreatment.
Product
Brilliance iCT SP (Model No. 728311, Software Version 4.7.0 or 4.7.2 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0351-2019·2018-11-07
Trader Joe's Hummus Recalled for Potential Salmonella and Listeria Contamination
Bakkavor Foods USA is recalling Trader Joe's Hummus quartets due to potential Salmonella and Listeria monocytogenes contamination. Consumers should discard the product.
Product
Trader Joe's Hummus quartet; 20 oz. plastic container; Spicy Hummus Roasted Garlic Hummus, Regular Hummus and Tomato Basil Hummus. Perishable, Keep Refrigerated. SKU 39570
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0307-2019·2018-11-07
Philips CT Scanner Software Recall for Misleading Calcium Score Reports
Philips is recalling 145 CT scanners with software version 4.2.0 because the Calcium Score report may display confusing plaque analyses, potentially leading to patient mistreatment.
Product
Brilliance Big Bore Radiology CT (Model No. 728244) software version 4.2.0 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0313-2019·2018-11-07
BD Max Instrument Recall for False Positive Candida Results
Becton Dickinson is recalling 49 refurbished BD Max instruments due to a confirmed trend of false positive Candida glabrata results when Trichomonas vaginalis is present.
Product
BD Max Instrument, Catalog Number 441916 441927 (refurbished instrument) - Product Usage: The BD MAX System, used in conjunction with appropriate extraction kits and reagents, is capable of automated extraction and purification of nucleic acids from multiple specimen types. The…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0077-2019·2018-11-07
Forager Project Organic Protein Plant Shake Recalled for Undeclared Almonds
Forager Project LLC is recalling 2,256 cases of Organic Protein Plant Shake due to undeclared tree nuts (almonds).
Product
Forager Project Organic Protein Plant Shake Nuts & Vanilla 12 fl oz. UPC: 8 14558 02038 6
Category
Food
Distribution
13 states
HighFDA (Devices)·Z-0305-2019·2018-11-07
Philips Brilliance iCT Scanners Recalled for Misleading Calcium Score Reports
Philips is recalling Brilliance iCT scanners because software errors create confusing calcium score reports that may lead to patient mistreatment.
Product
Brilliance iCT (Model No. 728306), Software Version 4.1.6 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0331-2019·2018-11-07
Buddy's Kitchen Mushroom & Thyme Flatbread Pizza Recalled for Contamination Risk
Buddy's Kitchen is recalling Mushroom & Thyme Flatbread Pizza due to potential Listeria or Salmonella contamination linked to a McCain Foods recall.
Product
Mushroom & Thyme Flatbread Pizza, Item 70610. Net Weight 7.65 lbs. 48-2.55 oz. portions. Keep Frozen. For institutional use only. Buddy's Kitchen, Inc., Burnsville, MN 55337
Category
Food
Distribution
8 states
HighFDA (Drugs)·D-0165-2019·2018-11-07
Pharm D Solutions Recalls Levocarnitine Injectable Due to Sterility Concerns
Pharm D Solutions is recalling Levocarnitine 170 mg/mL Injectable because the product lacks assurance of sterility. The recall covers 3,000 milliliters distributed nationwide.
Product
Levocarnitine 170 mg/mL Injectable, Pharm D Solutions, Houston, Texas --- NDC 69699-1617-10
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0332-2019·2018-11-07
Buddy's Kitchen Recalls Huevos Rancheros Benedict Due to Listeria Risk
Buddy's Kitchen is recalling Huevos Rancheros Style Benedict products due to potential Listeria or Salmonella contamination linked to a McCain Foods recall.
Product
Huevos Rancheros Style Benedict with Seasoned Black Beans, Item 70614. Net Weight 9.60 lbs. 24-6.40 oz. portions. Keep Frozen. For institutional use only. Buddy's Kitchen, Inc., Burnsville, MN 55337
Category
Food
Distribution
8 states
HighFDA (Drugs)·D-0190-2019·2018-11-07
Pharm D Solutions Recalls Tri-Mix XL Injectable Due to Sterility Concerns
Pharm D Solutions is recalling 553 vials of Tri-Mix XL injectable and powder nationwide due to a lack of assurance of sterility.
Product
Tri-Mix XL 150 mg/10 mg/100 mcg a) Injectable NDC 69699-1353-10; b) (LYO) Powder NDC 69699-1353-10, Pharm D Solutions, Houston, Texas
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0302-2019·2018-11-07
Philips Recalls Vereos PET/CT Software Due to Image Errors
Philips Medical Systems is recalling 61 units of Vereos PET/CT software version 2.0.1 due to errors that may produce incorrect images or disrupt procedures.
Product
Vereos PET/CT, Software version 2.0.1. Model Number: 882446 Product Usage: The Philips Vereos PET/CT system is a diagnostic imaging device that combines Positron Emission Tomography (PET) and X-ray Computed Tomography (CT) systems. The CT subsystem images anatomical…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0156-2019·2018-11-07
Pharm D Solutions Recalls HCG Lyophilized Injectable Due to Sterility Concerns
Pharm D Solutions is recalling 2,219 vials of HCG Lyophilized 5000 IU Injectable because the product lacks assurance of sterility.
Product
HCG Lyophilized 5000 IU Injectable Pharm D Solutions, Houston, Texas ---- NDC 69699-1707-10
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0308-2019·2018-11-07
Philips Ingenuity CT Software Recall for Misleading Calcium Score Reports
Philips is recalling Ingenuity CT scanners with software version 4.1.6 because the Calcium Score report may display confusing information, potentially leading to patient mistreatment.
Product
Ingenuity CT (Model No. 728326), software version 4.1.6 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0199-2019·2018-11-07
Pharm D Solutions Recalls Trimix Powder Due to Sterility Concerns
Pharm D Solutions is recalling 715 vials of Trimix powder nationwide due to a lack of assurance of sterility.
Product
Trimix Papaverine/Phentolamine/Alprostadil 30 mg/1 mg/10 mcg Powder Pharm D Solutions, Houston, Texas --- NDC 69699-1365-10
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0335-2019·2018-11-07
Buddy's Kitchen Recalls Frozen Stir Fry Wraps Due to Contamination Risk
Buddy's Kitchen is recalling frozen Stir Fry Wrap with Rice, Broccoli & Peppers due to potential Listeria or Salmonella contamination linked to a McCain Foods recall.
Product
Stir Fry Wrap with Rice, Broccoli & Peppers, Item 70668. Net Weight 17.50 lbs. 56 - 5.00 oz. portions. Keep Frozen. For institutional use only. Buddy's Kitchen, Inc., Burnsville, MN 55337
Category
Food
Distribution
8 states
HighFDA (Devices)·Z-0312-2019·2018-11-07
BD Max Instrument Reader Spare Part Recalled for False Positive Results
Becton Dickinson is recalling 23 BD Max Instrument Reader Spare Parts due to a confirmed trend of false positive Candida glabrata results.
Product
BD Max Instrument Reader Spare Part, Catalog Number 8090369/443364, 44336409 (Repaired Reader spare part) - Product Usage: The BD MAX System, used in conjunction with appropriate extraction kits and reagents, is capable of automated extraction and purification of nucleic acids…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0295-2019·2018-11-07
Arthrex Recalls Li-ion Battery Housings for AR-400 DrillSaw Sports 400 System
Arthrex, Inc. is recalling 335 Li-ion Battery Housings for the AR-400 DrillSaw Sports 400 System because they may not provide a complete seal, allowing for potential fluid ingress.
Product
Li-ion Battery Housing for AR-400 DrillSaw Sports 400 System Product Usage: The battery housing is used to house the battery that powers the AR-400 DrillSaw Sports 400 device.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0285-2019·2018-11-07
Magellan LeadCare II Blood Lead Test Kit Recalled for Calibration Defect
Magellan Diagnostics is recalling LeadCare II Blood Lead Test Kits because a calibration defect causes all patient results to display as HIGH.
Product
Magellan LeadCare¿ II Blood Lead Test Kit. In Vitro Test for the measurement of lead in fresh whole blood. Catalog Number: 70-6762 Primary DI No: 00850355006000 The LeadCare II Blood Lead Test Kit is for in vitro diagnostic use only. The test kit is for the quantitative…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0122-2019·2018-11-07
Sprayology Recalls ImmunoBooster Homeopathic Oral Spray Due to CGMP Deviations
Sprayology is recalling 2,837 bottles of ImmunoBooster Homeopathic Oral Spray nationwide due to manufacturing conditions that could result in microbial contamination.
Product
ImmunoBooster, Homeopathic Oral Spray 1.38 fl. oz. (41 mL). Manufactured by Sprayology Gaithersburg, MD 20879. NDC 61096-0038-1
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0309-2019·2018-11-07
Philips CT Scanner Software Recall for Misleading Calcium Score Reports
Philips is recalling Ingenuity Core CT scanners with software version 4.1.6 because the Calcium Score report may display confusing plaque analyses, potentially leading to patient mistreatment.
Product
Ingenuity Core (Model No. 728321), Software version 4.1.6 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0113-2019·2018-11-07
Sprayology Recalls DigestivEase Homeopathic Oral Spray Due to CGMP Deviations
Sprayology is recalling 1,465 bottles of DigestivEase Homeopathic Oral Spray due to manufacturing conditions that could result in microbial contamination.
Product
DigestivEase, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879.NDC 61096-0005-1
Category
Drug
Distribution
Distributed nationwide