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CareLink SmartSync™
MEDTRONIC, INC. · Model 24970A · UDI-DI 00763000201289
0
510(k) clearances
9
Adverse events (1 deaths)
2
Recalls
10
Facilities
Description
PROGRAMMER 24970A US MKT BASE ONLY
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2005-08-31 | Remington Medical Inc. | The vector selector has an electrical design flaw which prevents RV pacing. |
| 2004-10-20 | Medtronic Inc. Cardiac Rhythm Managment | A specific lot of leads are labeled incorrectly. The leads are 45 cm in length and labeled as 52 cm lead length. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.