Drug recall
ChannelCheck Convenience Pack, Model Numbers UCC-222CP and UCC-222-ESP (Sample)
FDA recall event 96823 · Class II · Healthmark Industries Co., Inc.
Key facts
| Event ID | 96823 |
|---|---|
| Recall numbers | Z-1909-2025, Z-1910-2025 |
| Recalling firm | Healthmark Industries Co., Inc. |
| Product type | Devices |
| Products | ChannelCheck Convenience Pack, Model Numbers UCC-222CP and UCC-222-ESP (Sample), Pre-filled Water Syringe, Model Numbers SW-010-100 and SW-010 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| 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… |
| Initiation date | May 2, 2025 |
| Report date | Jun 11, 2025 |
| City | Fraser |
| State | MI |
| Country | United States |
| FEI number | 1000160387 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: