FDA recall Z-2679-2026

Oscor Inc. · Class I · device

Product

Abiomed REF: 0052-3021, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Infusion Sideport, 14F, 23F. heart pump and accessories.

Reason for recall

Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines in the hub region.

Distribution

Distribution in the US state of MA

Key facts

Status
Ongoing
Initiation date
2026-06-10
Report date
2026-07-22
Voluntary/Mandated
Voluntary: Firm initiated
Location
Palm Harbor, FL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2679-2026