Transvenous Pacing Electrode TrayRecalls & reported problems across all models
Argon Medical Devices, Inc. · 2 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one Transvenous Pacing Electrode Tray model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 2 models of Transvenous Pacing Electrode Tray by Argon Medical Devices, Inc. in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
1 FDA recall record name at least one of these models by its device 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. 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
Transvenous Pacing Electrode Tray 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.
- Jun 1, 2026Open, Classified
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
Z-2704-2026 · Root cause: Material/Component Contamination · names 2 of these models · Recall details · FDA record ↗
Transvenous Pacing Electrode Tray models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Transvenous Pacing Electrode Tray 008416ACardiovascular Procedure Kit1 recall0 reports
- Transvenous Pacing Electrode Tray 008566ACardiovascular Procedure Kit1 recall0 reports
Other Argon Medical Devices, Inc. products
- First PICC S/L Peripherally Inserted Central Catheter5 models · 174 reports
- BioPince Ultra Full Core Biopsy Instrument10 models · 85 reports · 1 recall
- BioPince Full Core Biopsy Instrument5 models · 60 reports · 1 recall
- L-Cath PICC S/L2 models · 30 reports · 1 recall
- Tru-Core II Biopsy Instrument8 models · 13 reports · 1 recall
- Scorpion2 models · 7 reports · 1 recall
- Arterial Line Kit2 models · 2 reports · 1 recall
- Tru-Core II URO Biopsy Instrument2 models · 2 reports · 1 recall
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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