CardioCommand — Class III medical device recall Z-1773-2019
Terminated recall by Cardiocommand Inc., reported 2019-06-19, distributed nationwide. Possible corrosion of the battery contact(s).
| Recall number | Z-1773-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cardiocommand Inc., Tampa, FL, United States |
| Recall initiated | 2019-05-10 |
| Classified | 2019-06-12 |
| Reported by FDA | 2019-06-19 |
| Terminated | 2021-04-12 |
| Distributed | Nationwide (US) |
| Quantity | 5 units |
| Serial numbers | 8022, 8059, 8060, 8063, 8211 |
| Model numbers | 0101 |
Product
CardioCommand, Inc. Transesophageal Cardiac Pacing and Recording System, Model 7A, REF 0101 - Product Usage: Indications for Use: - Temporary left atrial pacing to treat bradycardia, hypotension or AV junctional rhythm - Acceleration of heart rate as an alternative to exercise or drugs during diagnostic cardiac studies such as echocardiography or radionuclide ventriculography. - Antitachycardia pacing for cardioversion of supraventricular tachycardia (SVT), including atrial flutter and re-entrant atrial or atrioventricular paroxysmal tachycardia. - Esophageal electrocardiography for differential diagnosis of complex atrial arrhythmia
Reason for recall
Possible corrosion of the battery contact(s).
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1773-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.