Home › Device types › LDF
Electrode, Pacemaker, Temporary
FDA product code LDF · Class 2 · Cardiovascular
501
Registered devices
2,012
Adverse events
15
Recalls
130
510(k) clearances
Devices with this code
SoloPace Fusion Ground Pad — SOLO PACE INC.Myo/Wire — A & E MEDICAL CORPORATIONMYLER™ Temporary Pacing Electrode Catheter — C. R. Bard, Inc.Myo/Wire — A & E MEDICAL CORPORATIONE-PACK — Ethicon Inc.E-PACK — Ethicon Inc.Flexon — Covidien LPHELIOS — Oscor Inc.E-PACK — Ethicon Inc.Temporary Myocardial Heartwire — Oscor Inc.TB — Oscor Inc.MYO/Wire® Ultra-Thin Temporary Pacing Wires — A & E MEDICAL CORPORATIONE-PACK — Ethicon Inc.E-PACK — Ethicon Inc.MYO/Wire® Ultra-Thin Temporary Pacing Wires — A & E MEDICAL CORPORATIONMYO/Wire® Ultra-Thin Temporary Pacing Wires — A & E MEDICAL CORPORATIONMyo/Wire — A & E MEDICAL CORPORATIONTB — Oscor Inc.Myo/Wire — A & E MEDICAL CORPORATIONNA — MEDTRONIC, INC.E-PACK — Ethicon Inc.NA — MEDTRONIC, INC.Myo/Wire — A & E MEDICAL CORPORATIONMyo/Wire — A & E MEDICAL CORPORATION
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-04-21 | ARROW INTERNATIONAL, LLC | Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality iss |
| 2024-04-08 | MEDLINE INDUSTRIES, LP - Northfield | Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have bee |
| 2024-04-08 | MEDLINE INDUSTRIES, LP - Northfield | Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have bee |
| 2024-04-08 | MEDLINE INDUSTRIES, LP - Northfield | Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have bee |
| 2019-06-21 | Alto Development Corp | Updated instructions for use: Ultra-Flex MYO/WIRE Monopolar pacing wire looped electrode (M-21 Series) to be consistent between electrode IFU and instructions |
| 2018-09-26 | Oscor, Inc. | During the use of some TB - Temporary Bipolar Pacing Leads, featuring the 2mm unshrouded connectors, the connector cap housing may slide and potentially expose |
| 2016-06-16 | Medtronic Inc., Cardiac Rhythm and Heart Failure | This Pacing Lead System does not comply with Section 8.5.2.3 of IEC 60601-1, and corresponding provisions of FDA 21 CFR 898, which relate to design standards to |
| 2013-04-26 | Heart Sync, Inc | On 4/18/13 HEARTSYNC became aware of a recall from their wire/connector sub-assembly supplier which is used in the C100-Physio Electrodes. There were reports of |
| 2013-04-26 | Heart Sync, Inc | On 4/18/13 HEARTSYNC became aware of a recall from their wire/connector sub-assembly supplier which is used in the C100-Physio Electrodes. There were reports of |
| 2012-07-25 | Oscor, Inc. | Oscor, Inc. in Palm Harbor, FL is recalling myocardial heart wires, models TME60S, TME64S, TME64C, TME64S-3, TME65S, and TME66S. The recall was initiated due to |
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