ADVANTA SLIDER GDS 22125Recalls & reported problems
Atrium Medical Corporation · 4-7MMX45CM, SW, SH, CH, ADVNTA VXT, GDS · Class 1 · Implant
All models of ADVANTA SLIDER GDS (51)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 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, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Recalls naming this device
- May 3, 2024Class IIOpen, 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 ↗
Other INSTRUMENTS, SURGICAL, CARDIOVASCULAR devices
- ACCESSRAIL Platform (Standard Blade) SB-1000Maquet Cardiovascular LLC · Instruments, Surgical, Cardiovascular1 recall6 reports
- ADVANTA SLIDER GDS 22025Atrium Medical Corporation · INSTRUMENTS, SURGICAL, CARDIOVASCULAR1 recall0 reports
- ADVANTA SLIDER GDS 22092Atrium Medical Corporation · INSTRUMENTS, SURGICAL, CARDIOVASCULAR1 recall0 reports
- Needle NDL-107-04Galt Medical Corp. · Instruments, Surgical, Cardiovascular1 recall0 reports
- Lead Clippers G20003Cook Vandergrift Inc. · INSTRUMENTS, SURGICAL, CARDIOVASCULAR1 recall0 reports
- PILLING IPN005932Teleflex Incorporated · INSTRUMENTS, SURGICAL, CARDIOVASCULAR18 reports
- PILLING IPN915270Teleflex Incorporated · INSTRUMENTS, SURGICAL, CARDIOVASCULAR16 reports
- NA APU544Medtronic, Inc. · INSTRUMENTS, SURGICAL, CARDIOVASCULAR5 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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