Recall Z-0222-2022— Cook Inc.
Class II · Terminated
Class II FDA medical device recall by Cook Inc., initiated 2021-10-08, terminated 2024-02-14. FDA's recall record names no specific 510(k) clearance for this event. Product: Transseptal Needle, Trocar. RPN TSNC-18-71.0, TSNC-19-56.0. GPN G02364, G02365. Product consists of a transseptal needle and obturator.. Reason: 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..
- Recalling firm
- Cook Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2021-10-08
- Terminated
- 2024-02-14
- Firm location
- Bloomington, IN, United States
Product description
Transseptal Needle, Trocar. RPN TSNC-18-71.0, TSNC-19-56.0. GPN G02364, G02365. Product consists of a transseptal needle and obturator.
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.