Home › MEDTRONIC, INC. › NA
NA
MEDTRONIC, INC. · Model 53922US · UDI-DI 00643169305120
DTE
Prescription
2
510(k) clearances
13,075
Adverse events (87 deaths)
5
Recalls
17
Facilities
Description
COVER EPG 53922US 3 PK MKT US
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2019-05-28 | Bio-Detek, Inc. | Some of the electrodes may have been assembled incorrectly, preventing delivery of defibrillation or pacing therapy. |
| 2018-06-06 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | A subset of Medtronic Model 53401 Single Chamber External Pulse Generators (EPGs) may revert from programmed settings to nominal settings during use with a patient due to an unexpe |
| 2015-03-17 | Medtronic Inc. Cardiac Rhythm Disease Management | Possible performance issue when used with specific AA-sized (LR6) batteries. The negative terminal of a commercially available AA (LR6) battery did not maintain a sufficient connec |
| 2010-06-30 | Osypka Medical Inc | The recall was initiated after Osypka Medical received two (2) complaints from their Japanese distributor regarding an incompatibility of the PACE 203H with some new types of 9 V b |
| 2010-06-30 | Osypka Medical Inc | The recall was initiated after Osypka Medical received two (2) complaints from their Japanese distributor regarding an incompatibility of the PACE 203H with some new types of 9 V b |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.