FDA recall Z-0223-2022

Cook Inc. · Class II · device

Product

Transseptal Needle with Catheter. RPN TSN-17-75.0-ENDRYS. GPN G19261. Coaxial set consisting of an outer catheter, curved-tip metal cannula, and a tapered-tip inner needle

Reason for recall

Transseptal needles may contain rust on the interior and/or exterior of the needle, which may not be detected by the user. Potential adverse events if an affected product is used ranges from increased procedural time to inflammatory reactions, which at their most severe include systemic reactions potentially leading to permanent impairment or death.

Distribution

Domestic distribution nationwide. Foreign distribution worldwide.

Key facts

Status
Terminated
Initiation date
2021-10-08
Report date
2021-11-24
Termination date
2024-02-14
Voluntary/Mandated
Voluntary: Firm initiated
Location
Bloomington, IN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0223-2022