Henke recalls sterile single-use syringes where the sterile barrier might be damaged, risking contamination. Affected lots: 22M28C8 and 23A09C8. Stop using immediately.
Sterile barrier might be damaged compromising the sterility of the device.
Henke is recalling sterile single-use syringes used for injections because the sterile barrier could be damaged, potentially compromising sterility. This risk is serious enough to require immediate action to prevent contamination.
The sterile barrier in these syringes might be damaged during use, which could allow contaminants to enter the syringe. This compromises the sterility of the device and could lead to infections or other health issues.
Healthcare professionals and patients who own or use Henke Ject-2 syringes with lot numbers 22M2:8C8 or 23A09C8 are affected. Those using the syringes for medical injections are most at risk.
Check for lot numbers 22M28C8 or 23A09C8 on the syringe packaging. The syringes are used for intravenous, intramuscular, subcutaneous, and intraarterial injections.
Discard any Henke Ject-2 syringes with lot numbers 22M28C8 or 23A09C8 to prevent potential contamination.
Lot numbers 22M28C8 and 23A09C8.
Yes, these syringes are used for intravenous, intramuscular, subcutaneous, and intraarterial injections.
Look for lot numbers 22M28C8 or 23A09C8 on the syringe packaging.
We’ve drafted a message you can send Henke to request your refund or repair — edit it as you like.
Subject: Recall Z-2642-2023 — Henke Henke Hello, I own a Henke that is covered by recall Z-2642-2023 from Henke. 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.
