Healthmark Industries Co., Inc.: Medical Device Recall in 2025 - (Recall #: Z-1910-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

ChannelCheck Convenience Pack, Model Numbers UCC-222CP and UCC-222-ESP (Sample)

Product Classification:

Class II

Date Initiated: May 2, 2025

Date Posted: June 11, 2025

Recall Number: Z-1910-2025

Event ID: 96823

Reason for Recall:

During endoscope surveillance monitoring, a user facility identified contamination from duodenoscope samples that were linked to the Pre-filled Water Syringes as part of their investigation. Healthmark Industries conducted its own investigation and concluded that the Pre-filled Water Syringe had been improperly used outside of the intended purpose.

Status: Ongoing

Product Quantity: 193035 units

Code Information:

Lot Numbers: 200014 200015 200016 900153 900154 900155 900156 900157 900158 900159 900160 900161 900162 900163 900164 900165 900166 900167 900168 900169 900170 900171 900172 900173 900174 900175 900176 900177 103564 103312 103293 102807 102096 101673

Distribution Pattern:

US Nationwide and Internationally to countries of: Canada, Malaysia.

Voluntary or Mandated:

Voluntary: Firm initiated