FDA recall Z-2002-2020

Product

Central Venous Catheters are indicated for the assessment of hemodynamic status through right atrial, right ventricular, and pulmonary artery and/or wedge pressure monitoring for patients. Model # 50456-01

Reason for recall

Inability for the guidewire to pass through the needles included with the catheter kits.

Distribution

US Consignees including in the states of AL, CA, FL, GA, IL, ME, MI, MN, MS, NC, NH, NM, NY, OH, TX, UT, VA and WA OUS - Canada.

Key facts

Status

Terminated

Initiation date

2020-01-02

Report date

2020-05-20

Termination date

2022-09-14

Voluntary/Mandated

Voluntary: Firm initiated

Location

San Clemente, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2002-2020