ADVANTA SLIDER GDS 22092Recalls & reported problems
Atrium Medical Corporation · 6MMX45CM, SW, CH, ADVANTA VXT, GDS · Class 1 · Implant
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. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- 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 · 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
- Lead Clippers G20003Cook Vandergrift Inc. · INSTRUMENTS, SURGICAL, CARDIOVASCULAR1 recall0 reports
- ADVANTA SLIDER GDS 22125Atrium Medical Corporation · INSTRUMENTS, SURGICAL, CARDIOVASCULAR1 recall0 reports
- Needle NDL-107-04Galt Medical Corp. · Instruments, Surgical, Cardiovascular1 recall0 reports
- PILLING IPN005932Teleflex Incorporated · INSTRUMENTS, SURGICAL, CARDIOVASCULAR18 reports
- PILLING IPN915270Teleflex Incorporated · INSTRUMENTS, SURGICAL, CARDIOVASCULAR16 reports
- PILLING IPN915271Teleflex Incorporated · INSTRUMENTS, SURGICAL, CARDIOVASCULAR5 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.