Data Foundry

Medical device recalls 2019

Medtronic Power Supply 26907 — Class II medical device recall Z-0845-2019

Terminated recall by Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF), reported 2019-02-27, distributed in GA. There is a potential for an electrical short circuit to develop in a subset of 479 Model 26907 power supply ca

Recall numberZ-0845-2019
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF), Mounds View, MN, United States
Recall initiated2019-01-17
Classified2019-02-16
Reported by FDA2019-02-27
Terminated2021-03-30
DistributedGA
Countries outside the USBG, HR, HU, IN, IR, JO, LB, LV, OM, PK, QA, RO, SA
Quantity731 units
Reason classesdevice malfunction
UPC / GTIN / UDI-DI00643169121973, 00643169166974, 00643169166981, 00643169166998, 00643169167001, 00643169167018, 00643169167025, 00643169167049, 00643169167063, 00643169167070, 00643169167087, 00643169167094, 00643169167100, 00643169225732, 00643169225749, 00643169225756, 00643169225763, 00643169225770, 00643169369030
Serial numbers00643169166981, 00643169166998, 00643169167001, 00643169167018, 00643169167025, 00643169167049, 00643169167063, 00643169167070, 00643169167087, 00643169167094, 00643169167100, 00643169225732, 00643169225749, 00643169225756, 00643169225763, 00643169225770, 00643169369030, 0643169166974, JVD000242P, JVD000243P, JVD000244P, JVD000245P, JVD000246P, JVD000247P, JVD000248P and 475 more

Product

Medtronic Power Supply 26907, Medtronic CareLink Encore(TM) 29901 Programmer

Reason for recall

There is a potential for an electrical short circuit to develop in a subset of 479 Model 26907 power supply cable plugs that connect to the Medtronic Model 29901 CareLink Encore programmer. A failure mode of the power supply has been found where an electrical short occurs on the low voltage direct current connector and results in the connector heating up, generating smoke, melting and in some cases disconnecting from the programmer.

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-0845-2019. 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.