Hobbs Medical, Inc.: Medical Device Recall in 2018 - (Recall #: Z-2052-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Hobbs Bronchial Cytology Brushes, Model Number 4202; 4204; 4206 To be utilized by a trained physician and/or trained personnel through a flexible endoscope when brush cell samples are required for cytological analysis.

Product Classification:

Class II

Date Initiated: May 1, 2018

Date Posted: June 13, 2018

Recall Number: Z-2052-2018

Event ID: 79903

Reason for Recall:

Device was marketed for uses outside the 510(k) clearance.

Status: Terminated

Product Quantity: 1820 devices

Code Information:

H07-17-157 H12-17-004 H10-17-055 H12-17-062 H11-17-101 H12-17-062 H11-17-119 H12-17-064 H11-17-120 H12-17-064 H11-17-121 H12-17-065 H11-17-122 H12-17-066 H11-17-123 H12-17-067 H11-17-124 H01-18-095 H11-17-125 H01-18-096 H11-17-126 H01-18-097 H11-17-127 H01-18-097 H11-17-128 H01-18-098 H11-17-129 H01-18-098 H11-17-130 H01-18-098 H12-17-002 H01-18-099 H12-17-003 H01-18-100 H12-17-003 H01-18-101 H01-18-102

Distribution Pattern:

US Nationwide Distribution to states of: AZ, CA, GA, IL, MD, NY, TN, TX, and VA.

Voluntary or Mandated:

Voluntary: Firm initiated