State

Georgia product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42926–42950 of 83444

SevereFDA (Drugs)·D-0931-2018·2018-07-25
Avella Recalls Epinephrine Bags Due to Potential Leakage and Sterility Concerns
Avella of Deer Valley is recalling 420 bags of Epinephrine 4 mg in 5% Dextrose due to potential leakage that compromises sterility.
Product
EPINEPHrine (USP) 4 mg, 5% Dextrose For Inj. (USP) 250 mL Volume: 254 mL single dose bag. For: Peninsular Regional Medical Center. By: Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054. NDC 15082-855-25.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0951-2018·2018-07-25
Avella Recalls Magnesium Sulfate Bags Due to Sterility Concerns
Avella of Deer Valley, Inc. is recalling 25 bags of Magnesium Sulfate in Sodium Chloride due to potential leakage and lack of sterility assurance.
Product
MAGnesium 1gm in NS 100 mL (MAGnesium SULfate (USP) 1 gm, 0.9% Sodium Chloride (USP) 100 mL). Volume: 102 mL. Single dose bag. For: Salt Lake Regional Med Ctr By: Avella of Houston, 9256 Kirby Dr., Houston, TX 77054. NDC: 42852-906-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0963-2018·2018-07-25
Avella Recalls Ephedrine Sulfate Syringes Due to Sterility Concerns
Avella of Deer Valley is recalling 10,500 ephedrine sulfate syringes nationwide due to potential bag leakage and lack of sterility assurance.
Product
ePHEDrine Sulfate, USP 25 mg in 0.9% Sodium Chloride, USP QS 5mL. Volume 5 mL Single dose syringe. Avella of Houston, 9265 Kirby Dr., Houston, TX 77054 NDC 42852-805-67
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0932-2018·2018-07-25
Avella Recalls Epinephrine Bags Due to Potential Leakage and Sterility Concerns
Avella of Deer Valley, Inc. is recalling 700 bags of Epinephrine (USP) 4 mg due to potential leakage that compromises sterility.
Product
EPINEPHrine (USP) 4 mg, 0.9% Sodium Chloride (USP) 250 mL Volume: 254 mL single dose bag. Avella of Houston, 9265 Kirby Dr., Houston, TX 77054. NDC 42852-823-25.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0941-2018·2018-07-25
Avella Recalls Vancomycin Bags Due to Potential Leakage
Avella of Deer Valley is recalling 1,352 bags of Vancomycin 1.25gm in D5W 250 mL due to potential leakage that compromises sterility.
Product
Vancomycin 1.25gm in D5W 250 mL. ( Vancomycin HCL (USP) 1.25 gm, 5% Dextrose Inj. (USP) 250 mL) Volume: 262 mL. Single dose bag. Avella Specialty Pharmacy, 24416N 19th Avenue, Phoenix, AZ 85085. NDC 42852-617-25
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0946-2018·2018-07-25
Avella Recalls Fentanyl and Ropivacaine Cassettes Due to Sterility Concerns
Avella of Deer Valley is recalling 100 fentanyl and ropivacaine cassettes due to potential bag leakage and lack of sterility assurance.
Product
fentaNYL 2 mcg/mL, 0.125% ROPivacaine, Fentanyl Citrate, USP 300 mcg, Ropivacaine HCL PF, USP 187.5 mg, 0.9% Sodium Chloride, USP QS 150 mL. Volume: 150 mL. Single dose cassette For: Methodist Dallas Medical Center. By: Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054. NDC…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2513-2018·2018-07-25
Medtronic Tri-Staple 2.0 Reloads Recalled for Missing Sled Component
Medtronic is recalling Tri-Staple 2.0 Intelligent Reloads because a missing sled component may prevent staple formation, leading to bleeding or leakage.
Product
Tri-Staple 2.0 Intelligent Reload for use with Signia stapling system 30 mm Medium/Thick, Item Code SIG30AMT
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2504-2018·2018-07-25
Medtronic Endo GIA Reloads Recalled for Missing Sled Component
Medtronic is recalling specific Endo GIA 60 mm reloads because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.
Product
Endo GIA 60 mm Articulating Medium/Thick Reload with Tri-StapleTechnology, Item Code EGIA60AMT
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2515-2018·2018-07-25
Medtronic Tri-Staple 2.0 Curved Tip Intelligent Reload Recall for Missing Sled
Medtronic is recalling Tri-Staple 2.0 Curved Tip Intelligent Reloads because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.
Product
Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia stapling system 45 mm Vascular/Medium, Item Code SIG45ACTAVM
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0933-2018·2018-07-25
Avella Recalls Fentanyl Syringes Due to Potential Leakage and Sterility Concerns
Avella of Deer Valley is recalling 120 fentanyl syringes due to potential bag leakage and lack of assurance of sterility.
Product
fentaNYL (10 mcg per mL) in 0.95 Sodium Chloride, USP QS 1mL. Volume 1mL. Single dose Syringe. For: Hunt Regional Medical Center, By: Advanced Pharma, 9265 Kirby Dr,., Houston, TX 77054. NDC 15082-210-70
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0954-2018·2018-07-25
Avella Recalls Morphine Syringes Due to Potential Sterility Compromise
Avella of Deer Valley, Inc. is recalling 740 single-dose Morphine 150 mg syringes due to a lack of assurance of sterility caused by potential bag leakage.
Product
MORphine 150 mg (Morphine Sulfate, USP 150mg in 0.9% Sodium Chloride, USP QS 30mL). Volume 30 mL. Single dose syringe. Avella of Houston, 9265 Kirby Dr., Houston, TX 77054. NDC 42852-243-63
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2501-2018·2018-07-25
Medtronic Recalls Visualase Cooled Laser Applicator Systems Due to Calibration Issues
Medtronic is recalling 1,283 Visualase Cooled Laser Applicator Systems because calibration errors may cause low laser energy output or fiber burnout.
Product
Visualase Cooled Laser Applicator System (VCLAS) labeled as: a. Part Number 9735559, Visualase¿ Cooled Laser Applicator System 3mm Tip; b. Part Number 9735560 Visualase¿ Cooled Laser Applicator System 10mm Tip; c. Part Number 9735561 Visualase¿ Cooled Laser Applicator…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0942-2018·2018-07-25
Avella Recalls Ropivacaine Infusion Bags Due to Sterility Concerns
Avella of Deer Valley, Inc. is recalling 20 bags of 0.2% Ropivacaine infusion cassettes due to potential leakage that compromises sterility.
Product
0.2% ROPivacaine, (Ropivacaine HCL PF, USP 500mg, 0.9% Sodium Chloride, USP QS 250 mL). Volume 250 mL. Single dose Cassette. For: Parkland Memorial Hospital. By: Advanced Pharma, 9225 Kirby Dr. Houston, TX 77054. Parkland Memorial Hospital NDC 15082-002-87
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0934-2018·2018-07-25
Avella Recalls Heparin Bags Due to Potential Leakage and Sterility Concerns
Avella of Deer Valley is recalling 240 bags of Heparin 25,000 Units in 5% Dextrose due to potential bag leakage and lack of sterility assurance.
Product
HEPARIN 25,000 Units in 5% Dextrose (Heparin Sodium, USP 25,000 Units, 5% Dextrose Inj., USP 250 mL) Volume: 255 mL. Single dose bag. Avella Specialty Pharmacy, 24416 N 19th Avenue, Pheonix AZ 85085. NDC 42852-729-25
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2494-2018·2018-07-25
Cardinal Health Recalls Hydroline Trumpet Valves Due to Suction Defect
Cardinal Health is recalling Hydroline Trumpet Valves because the suction valve may not close properly, potentially causing continuous suction.
Product
Hydroline Trumpet Valve, Trumpet Valve, No Probe, Single Spike, Ref ASU1220, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
Category
Medical Device
Distribution
34 states
HighFDA (Devices)·Z-2466-2018·2018-07-25
Ethicon Recalls Pronova Suture Due to Packaging Perforation Risk
Ethicon is recalling 516 units of Pronova Suture Blue because the needle may perforate the packaging, posing a risk of soft tissue injury or infection.
Product
PRONOVA SUTURE BLUE 122CM M1.5, D10189
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-2453-2018·2018-07-25
Ethicon Prolene Suture Recall Due to Packaging Perforation Risk
Ethicon is recalling specific Prolene suture products because a packaging design issue may allow needles to perforate the package, posing injury and infection risks.
Product
PROLENE SUTURE 36"(90CM) 4-0 BLUE, D7768
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-2449-2018·2018-07-25
Ethicon Proline Suture Recall Due to Packaging Perforation Risk
Ethicon is recalling 1,728 units of Proline suture because a packaging design issue allows needles to perforate the package, posing injury and infection risks.
Product
PROLENE SUTURE BLUE 4X90CM M1.5 USP 4/0 DA RB-1 +P, D5981
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-2488-2018·2018-07-25
Cardinal Health Recalls Hydroline Trumpet Valves Due to Suction Defect
Cardinal Health is recalling Hydroline Trumpet Valves because the suction valve may not close properly, potentially causing continuous suction.
Product
Hydroline Trumpet Valve with Pulse Wave Cassette, Trumpet Valve with Single Spike and no Probe, Ref ASC1220, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
Category
Medical Device
Distribution
34 states
HighFDA (Devices)·Z-2490-2018·2018-07-25
Cardinal Health Recalls Hydroline Trumpet Valves Due to Suction Defect
Cardinal Health 200, LLC is recalling Hydroline Trumpet Valves because the suction valve may not close properly, potentially causing continuous suction.
Product
Hydroline Trumpet Valve, Trumpet Valve, 5mm x 33cm Probe, Single Spike, Ref ASU1200, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
Category
Medical Device
Distribution
34 states
HighNHTSA·18E061000·2018-07-25
Rock Run Recalls LP Bottle Ring Brackets for Propane Tank Safety
Rock Run Industries is recalling LP Bottle Ring Brackets that may break, potentially causing propane cylinders to fall from vehicles.
Product
EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS:TANK ASSEMBLY recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0948-2018·2018-07-25
Avella Recalls Heparin Bags Due to Potential Leakage and Sterility Concerns
Avella of Deer Valley, Inc. is recalling 40 bags of Heparin 1,000 Units in NS 250mL due to potential leakage that compromises sterility.
Product
HEPARIN 1,000 Units in NS 250mL. (Heparin Sodium, USP 1,000 Units, 0.9% Sodium Chloride, USP 250 mL) Volume: 251 mL. Single dose bag. For: Adventist Medical Center Hanford. By: Avella of Huston, 9265 Kirby Dr., Houston TX, 77054. NDC 42852-747-25
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2441-2018·2018-07-25
Zeiss UV Disinfection Unit Recalled for Potential Radiation Exposure
Zeiss is recalling 8 UV disinfection units for the Celldiscoverer 7 microscope because a firmware issue may allow the unit to activate outside its housing, exposing users to harmful UV radiation.
Product
Disinfection unit UV (432332-9020-000) for the Celldiscoverer 7 microscope
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2487-2018·2018-07-25
Cardinal Health Recalls Hydroline Trumpet Valves Due to Suction Defect
Cardinal Health is recalling Hydroline Trumpet Valves because the suction valve may not close properly, potentially causing continuous suction.
Product
Hydroline Trumpet Valve with Pulse Wave Cassette, Trumpet Valve with Cassette, 5mm x 33cm Composite Probe, Double Spike, Ref ASC1201, packaged 1/box, 12 boxes/case, single use, RX, Sterile.
Category
Medical Device
Distribution
34 states
HighFDA (Food)·F-1656-2018·2018-07-25
Odwalla Superfood Fruit Smoothie Recalled for Potential Metal Fragments
The Coca-Cola Company is recalling Odwalla Superfood fruit smoothies due to the potential for tiny wire metal fragments in the bottles.
Product
Odwalla Superfood fruit smoothie 15.2 oz. (450mL) plastic bottle; Sold in 8 pack case Unit UPC: 000-14054-06405-5 Odwalla Life Food- Canada only - Unit UPC: 000-14054-03125-5 Ingredients: Apple Juice from concentrate, peach and mango purees from concentrate, banana…
Category
Food
Distribution
33 states