State

Georgia product recalls

73,495 recalls have nationwide distribution and so reach Georgia. 9,624 additional recalls listed Georgia specifically in their distribution scope.

What the numbers show

Total: 9,624
Critical: 1,474
Severe: 2,561
Most recent: 2026-10-14

Of the 9,624 recalls naming Georgia we have scored against our rubric, 1,474 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,561 (27%) are Severe.

Which agencies issued them

These figures cover only the 9,624 recalls whose distribution notice names Georgia specifically. The 73,495 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23076–23100 of 83119

HighFDA (Drugs)·D-0873-2022·2022-05-25
Accupril Quinapril HCl Tablets Recalled for Elevated Nitrosamine Impurity
Pfizer is recalling Accupril (Quinapril HCl) 20 mg tablets nationwide and in Puerto Rico due to N-nitrosoquinapril levels exceeding acceptable limits. Affected lots include DX8682 and DG1188.
Product
Accupril (Quinapril HCl Tablets) 20 mg, 90 Tablets, Rx only NDC 0071-0532-23 Distributed by: Parke-Davis Division of Pfizer Inc. NY, NY 10017
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1084-2022·2022-05-25
Medical Device Maker Recalls Laboratory Instrument With Incorrect Power Connector Rating
Beckman Coulter Inc. is recalling 7 MicroScan WalkAway-96 plus instruments due to an AC power connector rated for 1 ampere instead of the required 10 amperes. The underated connector could fail or overheat during normal operation.
Product
MicroScan WalkAway-96 plus Instrument REF B1018-284
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1089-2022·2022-05-25
Acetaminophen tablets in first aid kits recalled for contamination risk
Total Resources International first aid kits containing acetaminophen tablets are being recalled due to potential cross-contamination from manufacturing equipment damage at the tablet supplier.
Product
Total Resources International First Aid Kits, Item Numbers: 10HBC01087, 10HBC01092A3PK, 10HBC01112, 10HBC01113, 10HBC01329GLRV1, 10OUT02086GLRV2, 16BLU01495, 20HBC01015CCREV3, 20HBC01084GLOWCC. Kit contents include ULTRAtab Laboratories Coated APAP 325 mg (Acetaminophen 325…
Category
Drug
Distribution
30 states
HighFDA (Devices)·Z-1091-2022·2022-05-25
ATLAS Stim Headbox Recalled: Unapproved Investigational Device Without Safety Testing
Neuralynx is recalling the ATLAS Stim Headbox, a neurophysiology device distributed without FDA investigational approval or electrical safety clearance.
Product
ATLAS Stim Headbox-NK For use only with the ATLAS Neurophysiology System. CAUTION--INVESTIGATIONAL DEVICE Limited by Federal (or United States) law to investigational use. Only for use in Non-Significant Risk studies under the supervision of an IRB.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1085-2022·2022-05-25
Medical diagnostic instrument recalled for electrical connector assembly defect
Beckman Coulter is recalling 40 DxM 1040 MicroScan WalkAway laboratory instruments due to an assembly defect: some units have an AC power connector inlet rated at 1 ampere instead of the correct 10-ampere rating, which could impair power delivery.
Product
DxM 1040 MicroScan WalkAway Instrument REF B1018-440
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1116-2022·2022-05-25
Olympus Uretero-reno Videoscope Bending Section May Crack and Deform
The bending section of the Olympus URF-V2 videoscope may crack and develop abnormal shape or angulation. This could affect the device's function during urological procedures.
Product
Olympus Uretero-reno videoscope, Model No. URF-V2
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1112-2022·2022-05-25
VITROS Immunodiagnostic Hormone Reagents Recalled for Measurement Imprecision
Specific lots of VITROS FSH, LH, and Prolactin reagent kits may produce falsely high or delayed test results at low measurement levels. Affected lots distributed worldwide; labs should discontinue use and contact the manufacturer.
Product
VITROS Immunodiagnostic Products FSH Reagent Pack- IVD 1931922
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1114-2022·2022-05-25
VITROS Prolactin Reagent Recalled for Low-End Measurement Imprecision
Ortho-Clinical Diagnostics is recalling VITROS Prolactin Reagent packs due to low-end measurement imprecision that may cause falsely high or delayed test results. Approximately 1,767 affected units are distributed worldwide.
Product
VITROS Immunodiagnostic Products Prolactin Reagent Pack Product Code: 1849793
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1096-2022·2022-05-25
BioPlex 2200 CMV IgM Reagent Pack Recalled for Variable Test Performance
Bio-Rad Laboratories recalls the BioPlex 2200 ToRC IgM Reagent Pack (Lot 301388) due to CMV IgM analyte showing variable elevated background levels depending on reagent handling.
Product
BioPlex 2200 REF 12000670 ToRC IgM Reagent Pack
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1113-2022·2022-05-25
FDA Recalls VITROS Immunodiagnostic LH Reagent Pack for measurement imprecision
Ortho-Clinical Diagnostics is recalling VITROS Immunodiagnostic Products LH Reagent Pack due to low-end imprecision that may produce falsely high or delayed patient and quality control results.
Product
VITROS Immunodiagnostic Products LH Reagent Pack Product Code: 1350198
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1115-2022·2022-05-25
Radiometer Arterial Blood Sampler recalled due to sterility guarantee loss
Radiometer Medical is recalling Arterial Blood Samplers (REF:956-552) because sterility cannot be guaranteed throughout the product's shelf life. The recall affects 7,228 boxes distributed worldwide.
Product
Radiometer, REF:956-552, PIC050- Arterial Blood Sampler 1 X 2 mL, 80 IU electrolyte-balanced heparin. Not for injection. , IVD, Rx Only, Sterile EO, CE
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0874-2022·2022-05-25
Pfizer Accupril Blood Pressure Tablets Recalled for Nitrosamine Contamination
Pfizer is recalling specific lots of Accupril (quinapril HCl) 40 mg tablets distributed nationwide and in Puerto Rico because the product contains N-nitrosoquinapril above acceptable limits, a manufacturing deviation.
Product
Accupril (Quinapril HCl Tablets) 40 mg, 90 Tablets, Rx only NDC 0071-0535-23 Distributed by: Parke-Davis Division of Pfizer Inc. NY, NY 10017
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1083-2022·2022-05-25
MicroScan WalkAway-40 plus Instrument recalled for incorrect AC power connector
Beckman Coulter is recalling 22 MicroScan WalkAway-40 plus Instruments with an AC power entry connector rated at 1 ampere instead of the correct 10 amperes, creating a potential electrical hazard.
Product
MicroScan WalkAway-40 plus Instrument REF B1018-283
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1082-2022·2022-05-25
EXALT Model D Single-Use Duodenoscope: Updated Instructions for Perforation Risk
Boston Scientific issued updated instructions for the EXALT Model D Single-Use Duodenoscope to highlight the known risk of perforation and provide best practices for safe insertion, advancement, and removal.
Product
EXALT Model D Single-Use Duodenoscope (Box 2) UPN: M0054242CE1 Intended Use: sterile, single-use, flexible video duodenoscope intended for use with the EXALT" Controller to examine duodenum and perform various procedures within the duodenum including endoscopy and endoscopic…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1081-2022·2022-05-25
EXALT Model D Duodenoscope Updated Instructions Address Known Perforation Risk
Boston Scientific is updating instructions for the EXALT Model D Single-Use Duodenoscope to highlight the known risk of perforation during use and provide best clinical practices for insertion, advancement, and removal.
Product
EXALT Model D Single-Use Duodenoscope (Box 1) UPN:M0054242CE0 Intended Use: sterile, single-use, flexible video duodenoscope intended for use with the EXALT" Controller to examine duodenum and perform various procedures within the duodenum including endoscopy and endoscopic…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1078-2022·2022-05-25
Getinge Washer Disinfector models recalled for inadequate installation documentation
Getinge USA is recalling 127 Washer Disinfector models worldwide due to inadequate documentation verifying proper installation. The issue could lead to installation failures and potentially hazardous situations.
Product
Getinge 9100-Series Washer Disinfector models: 9120E, 9125E, 9127E, 9128E, 9122EW, 9128EW.
Category
Medical Device
Distribution
34 states
ModerateFDA (Drugs)·D-0880-2022·2022-05-25
Nitrofurantoin Capsules 100 mg recalled for failed dissolution specifications
American Health Packaging is recalling Nitrofurantoin Capsules 100 mg due to dissolution failure. The drug release results were above specification. No illnesses have been reported.
Product
Nitrofurantoin Capsules, USP (Monohydrate/Macrocrystals), 100 mg, 100 Capsules (10 x 10), 10-count blisters per card, 10 cards per carton, Unit Dose NDC 68084-446-11, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217, NDC: 68084-446-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1101-2022·2022-05-25
Medical Device Swabs Recalled Due to Manufacturing Validation Uncertainty
Convenience kits containing Prevantics swabs used in medical procedures are being recalled because the manufacturer failed to adequately validate the manufacturing test methods used during production.
Product
Prevantics swabs and/or swabsticks contained inside the following Aligned Medical Solutions convenience kits with Name/Pack numbers: Ports Cath Pack (1794)/AMS6569, Minor Procedure Pack (20527)/AMS6570B, Breast Biopsy Pack (24771)/AMS6572A, Bone Marrow Pack (11862)/AMS6573…
Category
Medical Device
Distribution
4 states
ModerateFDA (Devices)·Z-1080-2022·2022-05-25
EXALT Model D Single-Use Duodenoscope Updated Guidance on Perforation Risk
Boston Scientific updated instructions for the EXALT Model D Single-Use Duodenoscope to address the known risk of duodenal perforation and provide best clinical practices for proper insertion, advancement, and removal of the device.
Product
EXALT Model D Single- Use Duodenoscope (Box 2) UPN: M00542421 Intended Use: sterile, single-use, flexible video duodenoscope intended for use with the EXALT" Controller to examine duodenum and perform various procedures within the duodenum including endoscopy and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0881-2022·2022-05-25
Sirolimus Oral Solution Recalled for Failed Dissolution Specifications
Apotex Corp. recalls Sirolimus Oral Solution lot RZ1598 for exceeding dissolution specifications at the 14-month timepoint. Approximately 2,353 bottles were distributed nationwide.
Product
SIROLIMUS — SIROLIMUS (SIROLIMUS)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0872-2022·2022-05-25
Accupril tablets recalled by Pfizer for nitrosamine impurity
Pfizer is recalling 2,079 bottles of Accupril (Quinapril HCl) 10 mg tablets due to N-nitrosoquinapril exceeding acceptable limits. The affected lot was distributed nationwide and in Puerto Rico.
Product
Accupril (Quinapril HCl Tablets) 10 mg, 90 Tablets Rx only NDC 0071-0530-23 Distributed by: Parke-Davis Division of Pfizer Inc. NY, NY 10017
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1090-2022·2022-05-25
Total Resources International First Aid Kits Recalled Due to Cross-Contamination Risk
Total Resources International is recalling 891 First Aid Kits due to a potential cross-contamination issue from a manufacturing equipment breach. The kits contain electrolyte tablets that may have been exposed to pharmaceutical contaminants below therapeutic dose levels.
Product
Total Resources International First Aid Kits, Item Numbers: 01REF2621, 10OUT02086REV3. Kit contents include ULTRAtab Laboratories Electrolyte Tablets under the Brand of Medique and Medi-Lyte, Product Code: M963.
Category
Medical Device
Distribution
30 states
ModerateFDA (Devices)·Z-1110-2022·2022-05-25
Documentation errors recalled in HeartWare HVAD instructions and manuals
Medtronic is recalling instruction materials for the HeartWare HVAD ventricular assist device due to errors and inconsistencies in product documentation.
Product
Instructions for Use, Patient Manuals, and Emergency Responder Guides for HeartWare Ventricular Assist Device (HVAD) System. HVAD System. IFUs are distributed as part of the Pump Implant Kits models: 1103, MCS1705PU, 1104, and 1104JP. Additionally, IFUs, ERGs, and PMs are…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·22V371000·2022-05-24
Cross Country Recalls 2022 Trailers Due to Improperly Welded Couplers
Cross Country is recalling 2022 trailers because improperly welded couplers may cause the trailer to separate from the tow vehicle, increasing crash risk.
Product
CROSS COUNTRY — CROSS COUNTRY CROSS COUNTRY TRAILER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V370000·2022-05-24
Braun Ambulances Recall 2020-2021 Models Due to Lighting Failure Risk
Braun Ambulances is recalling 2020-2021 models because a defective circuit board can cause vehicle lighting to fail, increasing crash risk.
Product
BRAUN — BRAUN, BRAUN AMBULANCES TLC, EXPRESS PLUS TYPE I, CHIEF XL TYPE I
Category
Vehicle
Distribution
Distributed nationwide