State

Georgia product recalls

73,738 recalls have nationwide distribution and so reach Georgia. 9,632 additional recalls listed Georgia specifically in their distribution scope.

What the numbers show

Total: 9,632
Critical: 1,471
Severe: 2,565
Most recent: 2026-10-28

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.

35751–35775 of 83370

HighFDA (Devices)·Z-0139-2020·2019-10-23
ICU Medical Recalls Plum Microbore Infusion Sets Due to Fluid Leakage Risk
ICU Medical Inc is recalling 521 units of Plum Microbore Infusion Sets because air vents on inline filters may leak fluid. The recall covers nationwide and international distribution.
Product
Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as Primary PLUM Set, 15 Micron Filter in Sight Chamber, CLAVE Secondary Port, 0.2 Micron Filter, Polyethylene Lined Light Resistant Tubing, Distal Microbore Tubing, Secure…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0127-2020·2019-10-23
ICU Medical Recalls Plum Microbore Infusion Sets Due to Fluid Leakage
ICU Medical Inc is recalling specific Plum Microbore Infusion Sets because fluid may leak from the inline filter air vents.
Product
Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as Primary PLUM Set 0.2 Micron Filter, Prepierced Y-Site, Polyethylene Lined Light Resistant Tubing, Distal Microbore Tubing, Secure Lock, 104 Inch. 1 unit per pouch; 50…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0146-2020·2019-10-23
ICU Medical Recalls Sapphire Infusion Sets Due to Fluid Leakage Risk
ICU Medical Inc is recalling Sapphire Microbore Infusion Sets with Inline Filters due to a potential for fluid leakage out of air vents.
Product
Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Epidural Set with NRFit Connector Yellow-Striped Microbore, 0.2 Micron Filter 301 cm / 8.3 mL. 1 unit per blister; 40 blisters per case. Not distributed in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0036-2020·2019-10-23
Gullah Gourmet Recalls Nana's Been a Nut Bread for Missing Walnut Labeling
Gullah Gourmet, Inc. is recalling 673 bags of Nana's Been a Nut Bread because the ingredient statement does not list walnuts, posing a risk to consumers with walnut allergies.
Product
Nana's Been a Nut Bread NET WT. 11oz/311.74g cloth bag CONTAINS WHEAT AND SOY. MADE ON EQUIPMENT THAT MAKES PRODUCTS CONTAINING WHEAT, EGGS, MILK, SOY AND TREE NUTS. GULLAH BOURMET Inc. CHARLESTON, SC 29407 UPC 6 50305 01045 9
Category
Food
Distribution
16 states
HighNHTSA·19V755000·2019-10-23
BMW Recalls 2020 330i and M340i for Trunk Release Cable Defect
BMW is recalling 2020 330i and M340i vehicles because an improperly installed trunk release cable may prevent the trunk from opening from the inside.
Product
BMW — BMW 330I, M340I
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0143-2020·2019-10-23
ICU Medical Recalls Sapphire Microbore Infusion Sets Due to Leakage Risk
ICU Medical is recalling Sapphire Microbore Infusion Sets because fluid may leak from the inline filter air vents. The product was distributed in the U.S. and internationally.
Product
Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Epidural Set Yellow-Striped Microbore, 0.2 Micron Filter 301 cm / 8.3 mL. 1 unit per blister; 40 blisters per case . Not distributed in the U.S.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0125-2020·2019-10-23
OrthoPediatrics Recalls Adolescent Attachment Bolts Due to Interference Risk
OrthoPediatrics Corp is recalling 211 units of Adolescent attachment bolts used with the Pediatric Nailing Platform. The recall is due to potential interference between the bolt and nail, which may delay surgical procedures.
Product
OrthoPediatrics Adolescent attachment bolt used with the Pediatric Nailing Platform (PNP) targeting arm- intended as an orthopedic implant system (bolt is used to attach the targeting arm to the intramedullary fixation rod) Part number: 01-1503-0032
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0147-2020·2019-10-23
ICU Medical Recalls Sapphire Infusion Sets Due to Fluid Leakage Risk
ICU Medical is recalling Sapphire Microbore Infusion Sets because fluid may leak from the inline filters. The recall covers units distributed nationwide and internationally.
Product
Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Epidural Set with NRFit Connector Yellow-Striped Microbore, 0.2 Micron Filter, PAV, 123 Inch. 1 unit per pouch; 50 pouches per case
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0135-2020·2019-10-23
ICU Medical Recalls Sapphire Infusion Sets Due to Fluid Leakage Risk
ICU Medical is recalling Sapphire Microbore Infusion Sets because fluid may leak from the inline filters. The recall covers 4,600 units distributed nationwide and internationally.
Product
Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Epidural Set with NRFit Connector Yellow-Striped Microbore, 0.2 Micron Filter 119 Inch. 1 unit per pouch; 50 pouches per case
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0137-2020·2019-10-23
ICU Medical Recalls Plum Microbore Infusion Sets Due to Fluid Leakage Risk
ICU Medical Inc is recalling specific Plum Microbore Infusion Sets because fluid may leak from the inline filters. The affected units were distributed nationwide and internationally.
Product
Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as Primary PLUM Set 15 Micron Filter in Sight Chamber, CLAVE Secondary Port, 0.2 Micron Filter, CLAVE Y-Site, Polyethylene Lined Light Resistant Tubing, Distal Microbore…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0145-2020·2019-10-23
ICU Medical Recalls Plum Microbore Infusion Sets Due to Leakage Risk
ICU Medical Inc is recalling 7,920 units of Plum Microbore Infusion Sets because fluid may leak from the inline filters.
Product
Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as PLUM Epidural Set with NRFit Connector Yellow-Striped Tubing, Distal Microbore Tubing, 0.2 Micron Filter, 107 Inch. 1 unit per pouch; 48 pouches per case
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0148-2020·2019-10-23
Siemens Atellica CH 930 Analyzer Recalled for Erroneous Hemolysis and Lipemia Indices
Siemens Healthcare Diagnostics is recalling 1,125 Atellica CH 930 Analyzers worldwide due to software errors that may produce incorrect hemolysis and lipemia indices.
Product
Siemens Atellica CH 930 Analyzer. Siemens Material Number (SMN): 11067000 Product Usage: automated, clinical chemistry analyzer to perform in vitro diagnostic tests on clinical specimens
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0151-2020·2019-10-23
Xodus Medical Recalls Cautery Tip Cleaners Due to Sterile Barrier Concerns
Xodus Medical Inc is recalling 255,000 Cautery Tip Cleaners because the sterile barrier of some devices may have been affected.
Product
Cautery Tip Cleaner REF: 30500 Product Usage: electrosurgical accessory
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0150-2020·2019-10-23
Xodus Medical Recalls Electrosurgical Tip Cleaners Due to Sterile Barrier Concerns
Xodus Medical Inc is recalling 460,000 Electrosurgical Tip Cleaners because the sterile barrier of some devices may have been affected.
Product
Electrosurgical Tip Cleaner REF: 62-8499-001 Product Usage: electrosurgical accessory
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0159-2020·2019-10-23
Olympus Berkeley Disposa-Filter Recall Due to Weld Defect
Olympus is recalling Berkeley Disposa-Filters used with the VC-10 Vacuum Curettage System because an ultrasonic weld defect may cause the housing to separate.
Product
Berkeley Disposa-Filter used with Berkeley VC-10 Vacuum Curettage System - Product Usage: designed for rapid transcervical aspiration of the uterine cavity. Part# 54298-10/pack
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0158-2020·2019-10-23
Vital Scientific Selectra ProS Analyzer Recalled for Power Supply Failure
Vital Scientific is recalling six Selectra ProS Analyzers due to power supply failures that cause instrument malfunction and prevent the production of patient results.
Product
Selectra ProS Analyzer, Catalog # 6003-600/UDI # 03661540600418 Product Usage: :clinical chemistry system intended for use in clinical laboratories.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0155-2020·2019-10-23
Vital Scientific Viva-E Automated Chemistry Analyzer Recalled for Power Supply Failure
Vital Scientific N.V. is recalling 75 Viva-E automated chemistry analyzers due to power supply failures that prevent the instruments from producing patient results.
Product
Viva-E, Catalog # 6002-380, UDI # 03661540600050 Product Usage: automated chemistry analyzer intended for clinical use
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0156-2020·2019-10-23
Vital Scientific V-Twin Automated Chemistry Analyzer Recalled for Power Supply Failure
Vital Scientific N.V. is recalling 39 V-Twin automated chemistry analyzers due to a power supply failure that prevents the instruments from producing patient results.
Product
V-Twin, Catalog # 6002-800, UDI # 03661540600180 Product Usage: automated chemistry analyzer intended for clinical use
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0143-2020·2019-10-23
Aurobindo Recalls Amphetamine Mixed Salts Tablets for Out-of-Specification Weight
Aurobindo Pharma USA Inc. is recalling 11,129 bottles of 20mg Amphetamine Mixed Salts tablets because they failed weight and thickness specifications.
Product
DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0146-2020·2019-10-23
Ingenus Recalls Leucovorin Calcium Injection Due to Crystallization
Ingenus Pharmaceuticals is recalling Leucovorin Calcium Injection vials due to the presence of particulate matter identified as API crystallization.
Product
Leucovorin Calcium Injection, USP 500 mg*/50 mL (10 mg/mL) 50 mL Single-Dose Vial NDC 50742-464-50 Rx Only Ingenus Pharmaceuticals, LLC. Orlando, FL 32839
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0154-2020·2019-10-23
Vital Scientific Viva-JR Automated Chemistry Analyzer Recalled for Power Supply Failure
Vital Scientific N.V. is recalling four Viva-JR automated chemistry analyzers due to power supply failures that cause instrument malfunction and prevent the production of patient results.
Product
Viva - JR, catalog # 6002-940, UDI # 03661540600210 Product Usage: automated chemistry analyzer intended for clinical use
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0152-2020·2019-10-23
Roche Diagnostics Recalls cobas Integra Albumin Gen.2 Test Kits
Roche Diagnostics is recalling cobas Integra Albumin Gen.2 test kits due to low quality control recovery and invalid calibration.
Product
Roche Diagnostics cobas Integra Albumin Gen.2 Catalog Number: 05166861190 - Product Usage: In vitro test for the quantitative determination of the albumin in human serum and plasma on Roche/Hitachi cobas c systems.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0142-2020·2019-10-23
KVK-Tech Recalls Methylphenidate Hydrochloride Oral Solution Due to Foreign Particles
KVK-Tech is recalling 384 bottles of Methylphenidate Hydrochloride Oral Solution because of the presence of fiber particles.
Product
Methylphenidate Hydrochloride Oral Solution 5mg per 5mL, 500 mL Bottle, Sugar Free Alcohol Free, Rx Only, Mfd by: KVK Tech, Inc., Newtown, PA 18940, NDC 10702-0163-50.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0153-2020·2019-10-23
Roche Cobas c Bilirubin Total Gen.3 Recalled for Quality Control Issues
Roche Diagnostics is recalling 2,304 units of the Cobas c Bilirubin Total Gen.3 in vitro test due to low quality control recovery and invalid calibration.
Product
Cobas c Bilirubin Total Gen.3 Catalog Number: 05795419190 - Product Usage: In vitro test for the quantitative determination of the total bilirubin in serum and plasma of adults and neonates on Roche/Hitachi cobas c systems.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·20010·2019-10-22
Blackhawk T-Series L2C Gun Holsters Recalled for Injury Hazard
Federal Cartridge is recalling Blackhawk T-Series L2C gun holsters because the design can accidentally change a firearm's safety switch, posing an injury risk.
Product
Blackhawk T-Series L2C gun holsters
Category
Consumer Product
Distribution
Distributed nationwide