Stradis Healthcare recalls HCT 12 CC syringe kits with potential pinhole leaks near seals, risking sterility breaches. Affected kits have specific assembly numbers and lot numbers. Stop using immediately to avoid infection risks.
Potential for the outer bag having pinhole leaks near the seal, which may result in a breach in the sterility of the kit.
Stradis Healthcare is recalling HCT 12 CC syringe kits that may have pinhole leaks near the seal, which could breach sterility and cause infections. This is serious because medical kits must stay sterile for safe use.
The syringe kits may have pinhole leaks near the seal. If the seal is compromised, the kit could become contaminated, leading to infections during medical procedures.
Healthcare workers and patients using the recalled syringe kits. Those who have the specific assembly numbers or lot numbers listed are most at risk.
Check for assembly number HCT3548-2 or lot numbers listed: 222770947, 221809694, 221938965, 221748547, 221578546, 221808445, 221386002, 222859338, 222940522, 221938972.
Discard the recalled syringe kits to prevent potential contamination and infection risks.
The recall is due to potential pinhole leaks near the seal that could breach sterility, risking infections during medical procedures.
HCT 12 CC syringe kits with assembly number HCT3548-2 and lot numbers listed: 222770947, 221809694, 221938965, 221748547, 221578546, 221808445, 221386002, 222859338, 222940522, 221938972.
Check the assembly number on the kit (HCT3548-2) and lot numbers listed above.
We’ve drafted a message you can send Stradis Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0938-2023 — Stradis Healthcare Stradis Healthcare Hello, I own a Stradis Healthcare that is covered by recall Z-0938-2023 from Stradis Healthcare. 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.
