State

Georgia product recalls

73,734 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 73,734 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32601–32625 of 83366

HighFDA (Devices)·Z-1983-2020·2020-05-20
Access Scientific Recalls Saline Flush Syringes Due to Packaging Holes
Access Scientific LLC is recalling 110 units of BD PosiFlush SF Saline Flush Syringes because holes in the packaging compromised sterility.
Product
BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 5Fr 8cm Max Barrier Kit. REF/UDI / 94116/10859821006237 - Product Usage: is used to gain access to the vascular system to sample blood and administer fluids intravenously. It may be used for power injection of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1951-2020·2020-05-20
Cardiac Assist Recalls 38 TandemHeart ProtekDuo Kits Due to Assembly Error
Cardiac Assist, Inc. is recalling 38 TandemHeart ProtekDuo Kits because an assembly error may prevent the pump from priming.
Product
TandemHeart pump is assembled into kits: ProtekDuo Kit - DL29, Product: 5720-2916 - Product Usage: provides temporary extracorporeal circulatory system support with the unique ability to locally deliver an anticoagulant through the infusion system.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V290000·2020-05-20
Vac-Tron Vacuum Excavator Trailers Recalled for Lighting Defects
Vac-Tron is recalling 2016-2020 vacuum excavator trailers because front clearance lamps may be positioned improperly and reflectors may be missing, increasing crash risk.
Product
VAC-TRON — VAC-TRON LP 1273 XDT, CS 1270 GT, CS 1273 GT, CS 870 GT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1967-2020·2020-05-20
BD Alaris PCEA Administration Set Recalled for Potential Leaking
BD is recalling 110,350 Alaris PCEA Administration Sets because they may leak at the luer connection, potentially causing inadequate pain control.
Product
BD Alaris PCEA Administration Set, Microbore Tubing with Yellow Identification Stripe ASV, Catalog Number 30893-07 - Product Usage: Microbore Tubing with Yellow Identification Stripe Anti-siphon Valve Use Aseptic Technique Set cannot be used for gravity infusion. 1. Connect…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1956-2020·2020-05-20
Merit Medical Recalls Custom Sheath Introducer Kits Due to Labeling Error
Merit Medical Systems is recalling 15 Custom Sheath Introducer Kits because they were incorrectly labeled and contained the wrong sheath assembly.
Product
Custom Sheath Introducer Kit REF K21-00031 - Product Usage: intended use is to provide access and facilitate the percutaneous introduction of various devices into vein.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2007-2020·2020-05-20
Edwards Lifesciences Recalls Sterile Oxymetry Oligon Catheter Kits
Edwards Lifesciences is recalling 597 sterile catheter kits because their packaging was compromised, potentially affecting sterility.
Product
Sterile Oxymetry Oligon Catheter Kit. Pressure injectable. REF/UDI:XA3816SAFKT/ (01)00690103197181
Category
Medical Device
Distribution
15 states
ModerateFDA (Devices)·Z-1998-2020·2020-05-20
ICU Medical Recalls Central Venous Catheters Due to Guidewire Issue
ICU Medical is recalling 10 Central Venous Catheters because the included guidewire cannot pass through the needles.
Product
Central Venous Catheters are indicated for the assessment of hemodynamic status through right atrial, right ventricular, and pulmonary artery and/or wedge pressure monitoring for patients. Model # 41401-25.
Category
Medical Device
Distribution
19 states
ModerateFDA (Devices)·Z-1964-2020·2020-05-20
Bard PowerPort ClearVUE Slim Implantable Port Recalled for Incorrect Catheter Lock Size
Bard Peripheral Vascular Inc is recalling 200 units of PowerPort ClearVUE Slim Implantable Ports because the catheter locks may be 8Fr instead of the labeled 6Fr.
Product
BARD Access Systems PowerPort ClearVUE Slim Implantable Port With Smooth Septum and Attachable 6 F Polyurethane Open-Ended Single-Lumen Venous Catheter, Product #5676300 - Product Usage: All materials are biocompatible, can be used with virtually all injectable solutions…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1999-2020·2020-05-20
ICU Medical Recalls Central Venous Catheters Due to Guidewire Issue
ICU Medical is recalling 60 units of Model 41406-23 Central Venous Catheters because the included guidewires cannot pass through the needles.
Product
Central Venous Catheters are indicated for the assessment of hemodynamic status through right atrial, right ventricular, and pulmonary artery and/or wedge pressure monitoring for patients. Model # 41406-23
Category
Medical Device
Distribution
19 states
ModerateFDA (Devices)·Z-1928-2020·2020-05-20
Edwards HemoSphere Oximetry Cable Recalled for Inconsistent Connector Crimping
Edwards Lifesciences is recalling 35 HemoSphere oximetry cables due to intermittent communication caused by inconsistent crimping of connectors.
Product
Oxymetry Cable, Rxonly. REF/UDI: HEMOXSC100/(01)00690103196986 - Product Usage: The HemoSphere oximetry cable is a multi-use device that connects with a compatible Edwards monitor on one end and any approved Edwards oximetry catheter on the other end to continuously measure…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1942-2020·2020-05-20
Karl Storz Endoscopy Recalls Insufflation Tubing Due to Ethylene Oxide Residues
Karl Storz Endoscopy is recalling sterile insufflation tubing because it may contain higher ethylene oxide residues than the acceptable level.
Product
Insufflation tubing to be used with varies insufflator units. REF 031200-10; REF 031322-10; REF 031532-10; REF 031622-10
Category
Medical Device
Distribution
27 states
ModerateFDA (Devices)·Z-1970-2020·2020-05-20
C.R. Bard Recalls SureStep Foley Tray Systems Due to Residue
C.R. Bard is recalling 8,392 SureStep Foley Tray Systems because a white paper-type residue may be attached to the catheter.
Product
SureStep Foley Tray System - Product Usage: Intended for use in the drainage and/or collection and/or measurement of urine. Generally, drainage is accomplished by inserting the catheter through the urethra and into the bladder. However, drainage is sometimes accomplished by…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2002-2020·2020-05-20
ICU Medical Recalls Central Venous Catheters Due to Guidewire Issue
ICU Medical is recalling 15 units of Central Venous Catheters because the included guidewire cannot pass through the needles.
Product
Central Venous Catheters are indicated for the assessment of hemodynamic status through right atrial, right ventricular, and pulmonary artery and/or wedge pressure monitoring for patients. Model # 50456-01
Category
Medical Device
Distribution
19 states
ModerateFDA (Devices)·Z-2000-2020·2020-05-20
ICU Medical Recalls Central Venous Catheters Due to Guidewire Defect
ICU Medical is recalling 10 Central Venous Catheters because the included guidewire cannot pass through the needles. The defect prevents proper use of the device.
Product
Central Venous Catheters are indicated for the assessment of hemodynamic status through right atrial, right ventricular, and pulmonary artery and/or wedge pressure monitoring for patients. Model # 41411-25
Category
Medical Device
Distribution
19 states
ModerateFDA (Devices)·Z-2001-2020·2020-05-20
ICU Medical Recalls Central Venous Catheters Due to Guidewire Issue
ICU Medical is recalling 235 Central Venous Catheters because the included guidewire cannot pass through the needles.
Product
Central Venous Catheters are indicated for the assessment of hemodynamic status through right atrial, right ventricular, and pulmonary artery and/or wedge pressure monitoring for patients. Model # 41414-23
Category
Medical Device
Distribution
19 states
ModerateFDA (Devices)·Z-1971-2020·2020-05-20
BD Biosciences Recalls CD45 Reagent Due to False Positive Reactions
Becton, Dickinson and Company is recalling 1,473 vials of Analyte specific reagent (CD45) because of false positive reactions. The product is used for in vitro diagnostic testing.
Product
Analyte specific reagent. REF/UDI: 641408/641408-4012-1-1 (US); 641417/641417-1157-1-01 (OUS); 641399/641399-4012-1-01 (US Research Use Only) - Product Usage: CD45 is intended for in vitro diagnostic use in the identification of cells expressing the CD45 antigen, using a BD FAC…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1997-2020·2020-05-20
ICU Medical Recalls Central Venous Catheters Due to Guidewire Defect
ICU Medical is recalling 260 units of Central Venous Catheters because the included guidewire cannot pass through the needles.
Product
Central Venous Catheters are indicated for the assessment of hemodynamic status through right atrial, right ventricular, and pulmonary artery and/or wedge pressure monitoring for patients. Model # 41401-23.
Category
Medical Device
Distribution
19 states
ModerateFDA (Devices)·Z-1996-2020·2020-05-20
ICU Medical Recalls Central Venous Catheters Due to Guidewire Issue
ICU Medical is recalling 20 Central Venous Catheters because the included guidewire cannot pass through the needles. The product was distributed to US consignees and Canada.
Product
Central Venous Catheters are indicated for the assessment of hemodynamic status through right atrial, right ventricular, and pulmonary artery and/or wedge pressure monitoring for patients. LOT Number 4330832. Product not distributed in US, UDI: 1 0840619 04197 4
Category
Medical Device
Distribution
19 states
ModerateFDA (Devices)·Z-2006-2020·2020-05-20
Ra Medical Systems Recalls DABRA Catheters Due to Calibration Failure Risk
Ra Medical Systems is recalling DABRA catheters because the actual shelf life is shorter than labeled, potentially causing calibration failures.
Product
Ra Medical Systems DABRA Catheter 5F (1.5mm), REF: 1222-5000-01, LOT: 18-090400-094, USE BY: 2019-09-24, MFR DATE: 2018-09-24, CE, Laser Radiation, STERILE (Gamma Sterilized), Single Use Only Revised Label: Product Label - Ra Medical Systems DABRA Catheter 5F (1.5mm)…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1930-2020·2020-05-20
Ortho-Clinical Diagnostics Recalls VITROS CKMB Slides Due to Incorrect Instructions
Ortho-Clinical Diagnostics is recalling VITROS CKMB Slides because Spanish and Swedish instructions incorrectly state the assay can be tested with plasma, which could result in biased results.
Product
VITROS Chemistry Products CKMB Slides, Creatine Kinase MB, Product Code 805 8232-300 slides, UDI Number 10758750004294 - Product Usage: The VITROS Chemistry Product Slides are used to measure creatine kinase MB (CK-MB) activity in serum which used to be ordered to detect…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2005-2020·2020-05-20
Genicon EZee Specimen Retrieval Bag Recall for Labeling Clarity
Genicon is recalling 1,550 units of the EZee Single Use Specimen Retrieval Bag to provide updated labeling instructions for multiple specimen retrieval.
Product
Genicon EZee Single Use Specimen Retrieval Bag - Product Usage: This device is disposable and is packaged and sterilized for single use only. The bag may be used for multiple specimen retraction.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1949-2020·2020-05-20
Cardiac Assist Recalls TandemHeart Kits Due to Assembly Error
Cardiac Assist, Inc. is recalling five TandemHeart pump kits because an assembly error may prevent the device from priming.
Product
TandemHeart pump is assembled into kits: TandemHeart Kit - TS62/A15, Product: 5710-6215 - Product Usage: provides temporary extracorporeal circulatory system support with the unique ability to locally deliver an anticoagulant through the infusion system.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1931-2020·2020-05-20
Ortho-Clinical Diagnostics Recalls VITROS CKMB Slides Due to Incorrect Instructions
Ortho-Clinical Diagnostics is recalling VITROS CKMB Slides because Spanish and Swedish instructions incorrectly state the assay can be tested with plasma, which could result in biased results.
Product
VITROS Chemistry Products CKMB Slides, Creatine Kinase MB, Product Code 8001133-90 slides, UDI Number 10758750004201 - Product Usage: The VITROS Chemistry Product Slides are used to measure creatine kinase MB (CK-MB) activity in serum which used to be ordered to detect…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1941-2020·2020-05-20
Medtronic Recalls Vertex Select Multi Axial Screws Due to Length Discrepancy
Medtronic is recalling 83 Vertex Select Multi Axial Screws because the product length is shorter than labeled. The recall covers units distributed in California and Michigan.
Product
VERTEX SELECT MULTI AXIAL SCREW. 4.0 X 38MM MULTI AXIAL SCREW. Lot H5517628
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1946-2020·2020-05-20
Becton Dickinson Recalls PowerGlide ST Midline Catheter Kits Missing Lidocaine
Becton Dickinson is recalling 655 PowerGlide ST Midline Catheter Maximal Barrier Kits because they were packaged without the required lidocaine.
Product
PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length Catalog Number: ST018101D
Category
Medical Device
Distribution
14 states