Prodimed Plastimed Division: Medical Device Recall in 2020 - (Recall #: Z-2490-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Prodimed Combicath catheters for blind or fibrescope-guided protected distal bronchial sampling (PDBS)- COMBICATH PE 90 cm Product Code: 58229 19

Product Classification:

Class II

Date Initiated: May 27, 2020

Date Posted: July 15, 2020

Recall Number: Z-2490-2020

Event ID: 85776

Reason for Recall:

Lack of assurance of sterility

Status: Terminated

Product Quantity: 1460

Code Information:

All lots within expiry

Distribution Pattern:

Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated