B. Braun recalls 10ml sterile NORM-JECT Luer Solo syringes due to potential packaging damage that could compromise sterility. Affected units have specific lot numbers and were distributed by Air-Tite Products Co., Inc.
The sterile blister packaging may be damaged, and sterility may be compromised
B. Braun is recalling 10ml sterile N:ORM-JECT Luer Solo syringes because the packaging might be damaged, risking contamination. This could lead to infections if the syringe is used without proper sterility.
The sterile blister packaging may become damaged during handling or shipping, which could allow contaminants to enter the syringe. This might compromise sterility and increase infection risk if the syringe is used without proper cleaning.
Healthcare professionals and patients using the NORM-JECT Luer Solo syringes for medical injections or fluid withdrawal. Those with the specific lot numbers mentioned in the recall are most at risk.
Check for lot numbers 22M28C8 or 23A09C8 on the packaging. The product is a 10ml sterile syringe intended for medical use, distributed by Air-Tite Products Co., Inc.
Look for lot numbers 22M28C8 or 23A09C8 on the sterile blister packaging.
The recall states the packaging may be damaged, risking sterility. If you have the affected lot numbers, stop using it until you contact B. Braun.
Check the lot number on the packaging; affected units have lot numbers 22M28C8 or 23A09C8.
The recall does not specify a remedy, so contact B. Braun directly for guidance.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-2643-2023 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-2643-2023 from B. Braun. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
