ADVANTA SLIDER GDSRecalls & reported problems across all models
Atrium Medical Corporation · 51 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
51 open recalls name at least one ADVANTA SLIDER GDS model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 76
- Deaths reported
- 1
- Injuries reported
- 29
- Recalls
- 51
We found 51 models of ADVANTA SLIDER GDS by Atrium Medical Corporation in the FDA's device registry (GUDID). Together they are named in 76 adverse event reports in the FDA's MAUDE database, received between Jul 27, 2016 and Sep 29, 2026 — classified as 1 death, 29 injuries, 46 malfunctions.
The most frequently reported specific device problem is “Obstruction of Flow” (17 reports).
51 FDA recall records name at least one of these models by its device identifier, 51 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
ADVANTA SLIDER GDS recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-2001-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-2000-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1999-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1998-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1997-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1996-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1995-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1994-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1993-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1992-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1991-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1990-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1989-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1988-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1987-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1986-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1985-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1984-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1983-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1982-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1981-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1980-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1979-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1978-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1977-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1976-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1975-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1974-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1973-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
- May 3, 2024Open, Classified
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Z-1972-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
…and 21 older recalls, listed on each model's page.
Most reported ADVANTA SLIDER GDS problems
Device problems
- Obstruction of Flow17
- Material Separation10
- Device Operates Differently Than Expected5
- Material Deformation5
- Material Integrity Problem5
- Peeled/Delaminated5
- Adverse Event Without Identified Device or Use Problem4
- Detachment of Device or Device Component4
Patient problems
- No Clinical Signs, Symptoms or Conditions28
- Obstruction/Occlusion10
- No Known Impact Or Consequence To Patient8
- No Information7
- Limb Pain6
- Insufficient Information4
- Thrombosis/Thrombus4
- Hematoma3
ADVANTA SLIDER GDS models
51 models, most reported first. Each model has its own page with its reports, recalls and device details.
- ADVANTA SLIDER GDS 22114PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall11 reports
- ADVANTA SLIDER GDS 22115PROSTHESIS, VASCULAR GRAFT, OF LESS THEN 6MM DIAMETER1 recall9 reports
- ADVANTA SLIDER GDS 22222PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall8 reports
- ADVANTA SLIDER GDS 22187PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall6 reports
- ADVANTA SLIDER GDS 22012PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall5 reports
- ADVANTA SLIDER GDS 22064PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall5 reports
- ADVANTA SLIDER GDS 22221PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall1 death5 reports
- ADVANTA SLIDER GDS 22072PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall4 reports
- ADVANTA SLIDER GDS 22062PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall3 reports
- ADVANTA SLIDER GDS 22209PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall3 reports
- ADVANTA SLIDER GDS 22059PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall2 reports
- ADVANTA SLIDER GDS 22075PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall2 reports
- ADVANTA SLIDER GDS 22185PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall2 reports
- ADVANTA SLIDER GDS 22186PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall2 reports
- ADVANTA SLIDER GDS 22225PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall2 reports
- ADVANTA SLIDER GDS 22227PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall2 reports
- ADVANTA SLIDER GDS 22063PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall1 report
- ADVANTA SLIDER GDS 22116PROSTHESIS, VASCULAR GRAFT, OF LESS THEN 6MM DIAMETER1 recall1 report
- ADVANTA SLIDER GDS 22176PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall1 report
- ADVANTA SLIDER GDS 22212PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall1 report
- ADVANTA SLIDER GDS 22214PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall1 report
- ADVANTA SLIDER GDS 22011PROSTHESIS, VASCULAR GRAFT, OF LESS THEN 6MM DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22014PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22016PROSTHESIS, VASCULAR GRAFT, OF LESS THEN 6MM DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22017PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22018PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22019PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22025INSTRUMENTS, SURGICAL, CARDIOVASCULAR1 recall0 reports
- ADVANTA SLIDER GDS 22026PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22027PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22028PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22058PROSTHESIS, VASCULAR GRAFT, OF LESS THEN 6MM DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22061PROSTHESIS, VASCULAR GRAFT, OF LESS THEN 6MM DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22070PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22071PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22076PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22092INSTRUMENTS, SURGICAL, CARDIOVASCULAR1 recall0 reports
- ADVANTA SLIDER GDS 22117PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22124PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22125INSTRUMENTS, SURGICAL, CARDIOVASCULAR1 recall0 reports
- ADVANTA SLIDER GDS 22169PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22170PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22175PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22190PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22192PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22213PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22220PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22232PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22266PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22267PROSTHESIS, VASCULAR GRAFT, OF LESS THEN 6MM DIAMETER1 recall0 reports
- ADVANTA SLIDER GDS 22297PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall0 reports
Recent ADVANTA SLIDER GDS adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjurySep 29, 2026Obstruction of Flow
As part of Post-Market Clinical Follow-up (PMCF) Registry for VXT and Flixene Grafts the following adverse event information was provided regarding a VXT graft.It was reported that following implantation of an Advanta VXT vascular graft, the patient developed pain in the left lower limb after gardening while crouching for an extended period. Doppler ultrasound confirmed thrombosis of the bypass graft. Clinical symptoms included a cyanotic, cold, and painful leg and foot.The patient underwent a successful percutaneous graft reintervention on (b)(6) 2020, including endovascular pharmacological thrombolysis. Graft patency was restored, no amputation was required. The adverse event subsequently resolved.
Patient problems: Limb Pain; Thrombosis/Thrombus
MAUDE report 50930507 ↗InjurySep 25, 2026Obstruction of Flow
As part of Post-Market Clinical Follow-up (PMCF) Registry for VXT and Flixene Grafts the following adverse event information was provided regarding a VXT graft.It was reported that the patient experienced a decline in walking distance. Diagnostic evaluation by duplex ultrasound revealed occlusion of the femoro-femoral bypass graft, and a new crossover bypass was indicated. On (b)(6)2019, the patient underwent surgical reintervention, including explantation of the occluded graft and implantation of a new bypass graft. Blood flow was successfully restored, no amputation was required, and the event was reported as resolved following the procedure.
Patient problems: Obstruction/Occlusion
MAUDE report 50895279 ↗InjurySep 19, 2026Obstruction of Flow
Patient problems: Bacterial Infection
MAUDE report 50832636 ↗InjurySep 18, 2026Patient-Device Incompatibility
As part of Post-Market Clinical Follow-up (PMCF) Registry for VXT and Flixene Grafts the following adverse event information was provided regarding a VXT graft.The patient developed an infection of the left anterior femorotibial prosthesis, requiring graft removal and revascularization. On (b)(6) 2019, swelling was noted at the Scarpa approach, with a large inflammatory mass and underlying hematoma. Clinical findings included fever (38.2°C) and elevated inflammatory markers (CRP 150 mg/L). Bacteriological analysis confirmed penicillin-resistant Staphylococcus aureus infection. An infectious disease consultation on (b)(6) 2019 confirmed infection of the left anterior femorotibial prosthesis.A surgical reintervention was successfully performed on (b)(6) 2019 and included graft explantation and revascularization using a vein graft. No amputation was required. Following the procedure, patency was restored, and the adverse event resolved.
Patient problems: Drug Resistant Bacterial Infection
MAUDE report 50820383 ↗InjurySep 18, 2026Obstruction of Flow
As part of Post-Market Clinical Follow-up (PMCF) Registry for VXT and Flixene Grafts the following adverse event information was provided regarding a VXT graft.The patient developed acute lower extremity ischemia and presented with severe lower back pain radiating into both legs. On evaluation, the lower extremities were cold and tender, with absent palpable pulses and no sensory or motor deficits. CT angiography revealed a thrombus extending from the infrarenal aorta to the bilateral common iliac arteries.The patient underwent emergency surgical intervention, including a left axillo-femoral bypass and bilateral iliac, superficial femoral, deep femoral, and cross-bypass thrombectomies. A graft reintervention consisting of endovascular thrombectomy was successfully performed on (b)(6) 2022. Patency was restored, no amputation was required, and the adverse event subsequently resolved.
Patient problems: Ischemia; Limb Pain; Thromboembolism
MAUDE report 50816245 ↗InjurySep 12, 2026No Apparent Adverse Event
Patient problems: Hematoma
MAUDE report 50745773 ↗InjurySep 12, 2026Patient-Device Incompatibility
Patient problems: Bacterial Infection
MAUDE report 50745772 ↗InjurySep 12, 2026Obstruction of Flow
Patient problems: Limb Pain; Obstruction/Occlusion
MAUDE report 50745771 ↗InjurySep 12, 2026Obstruction of Flow
Patient problems: Limb Pain; Obstruction/Occlusion
MAUDE report 50745770 ↗InjurySep 11, 2026Obstruction of Flow
Patient problems: Implant Pain; Obstruction/Occlusion; Thrombosis/Thrombus
MAUDE report 50740338 ↗InjurySep 11, 2026Obstruction of Flow
Patient problems: Obstruction/Occlusion
MAUDE report 50740336 ↗InjurySep 11, 2026Obstruction of Flow
Patient problems: Obstruction/Occlusion
MAUDE report 50740335 ↗InjurySep 11, 2026Obstruction of Flow
Patient problems: Ischemia; Limb Pain; Thrombosis/Thrombus
MAUDE report 50739454 ↗InjuryAug 31, 2026Obstruction of Flow
As part of Post-Market Clinical Follow-up (PMCF) Registry for VXT and Flixene Grafts the following adverse event information was provided regarding a VXT graft.The patient underwent a Duplex ultrasound, which confirmed occlusion of the femoropopliteal bypass graft. Based on the findings, surgical intervention was planned. A successful percutaneous procedure was performed on (b)(6) 2026 to treat the occlusion. Following the procedure, the adverse event resolved without further reported complications.
Patient problems: Obstruction/Occlusion
MAUDE report 50519560 ↗InjuryAug 31, 2026Obstruction of Flow
As part of Post-Market Clinical Follow-up (PMCF) Registry for VXT and Flixene Grafts the following adverse event information was provided regarding a VXT graft.The patient underwent a CT scan that revealed occlusion of the lower limb arteries. Treatment was initiated with a femoroperoneal bypass and aponeurotomies however the patient's condition deteriorated, resulting in muscle compartment necrosis. On (b)(6) 2020, a surgical reintervention was performed, which included target limb amputation at or above the ankle. No procedural complications were reported, and the reintervention was considered successful. The adverse event was reported as resolved with sequelae.
Patient problems: Necrosis; Obstruction/Occlusion
MAUDE report 50519457 ↗
Other Atrium Medical Corporation products
All Atrium Medical Corporation devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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