Stradis Healthcare recalls HCT 6 CC syringe kits with potential pinhole leaks near seals, risking sterility breaches. Affected kits include specific lot numbers and assembly codes. Consumers should check their product details.
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 6 CC syringe kits that may have pinhole leaks near the seal. This could breach the sterility of the kit, posing a risk of infection during medical use.
The outer bag may develop pinhole leaks near the seal, which could compromise the sterility of the syringe kit. If the kit is not sterile, it could lead to infections during medical procedures.
Healthcare professionals and patients using the recalled syringe kits for medical injections. Those with the specific lot numbers or assembly codes listed are most at risk.
Check for assembly number HCT3916-1, UDI-DI: M752HCT391611, and lot numbers listed in the recall (222491279, 220113056, etc.). The product is sold in 5 bags per case.
Verify your syringe kit's assembly number and lot numbers against the list provided in the recall notice.
The recall is due to potential pinhole leaks near the seal that could breach the sterility of the kit, risking infection during medical use.
Affected lot numbers include 222491279, 220113056, 222782510, 221306003, 220051819, 222149971, 222210292, 221245035, and 221458554.
Check for assembly number HCT3916-1, UDI-DI: M752HCT391611, and the specific lot numbers listed in the recall notice.
We’ve drafted a message you can send Stradis Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0939-2023 — Stradis Healthcare Stradis Healthcare Hello, I own a Stradis Healthcare that is covered by recall Z-0939-2023 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.
