Healthmark recalls ChannelCheck Convenience Pack models UCC-222CP and UCC-222-ESP due to contamination risks from pre-filled water syringes used outside intended purpose.
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.
Healthmark is recalling ChannelCheck Convenience Pack models UCC-222CP and UCC-222-ESP after finding contamination linked to pre-filled water syringes. This recall matters because improper use of the syringes outside their intended purpose could lead to contamination risks.
The recall stems from contamination found in duodenoscope samples linked to pre-filled water syringes. Healthmark determined the syringes were improperly used outside their intended purpose, which could lead to contamination risks.
Users of ChannelCheck Convenience Pack models UCC-222CP and UCC-222-ESP are affected. Medical facilities using these products for endoscope surveillance may be at higher risk due to contamination concerns.
Check for ChannelCheck Convenience Pack models UCC-222CP and UCC-222-ESP. The product was sold with specific lot numbers listed in the recall notice.
Identify your ChannelCheck Convenience Pack model number and lot number to confirm if it's affected.
Healthmark identified contamination in duodenoscope samples linked to pre-filled water syringes used outside their intended purpose.
ChannelCheck Convenience Pack models UCC-222CP and UCC-222-ESP with specific lot numbers listed in the recall notice.
The recall does not specify a stop-use action; check product details to see if it's affected.
We’ve drafted a message you can send Healthmark to request your refund or repair — edit it as you like.
Subject: Recall Z-1910-2025 — Healthmark Healthmark Hello, I own a Healthmark that is covered by recall Z-1910-2025 from Healthmark. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
