RanD recalls Hang&Go kits (Reference Code R9900120) with specific lot numbers due to possible non-sterile products. Affected users should check their lot numbers and contact RanD for guidance.
The sterilization contractor informed the company of a quality issue possibly affecting the sterilization process of a certain number of products. It was determined that some lots may not be sterile.
RanD is recalling certain Hang&Go kits (Reference Code R9900120) because some lots may not be sterile. This could pose a health risk if used in medical procedures requiring sterile conditions.
The sterilization contractor reported that some lots of the kits may not be sterile. This means the products could cause infections or other complications during medical procedures if used without proper sterility.
Medical professionals using Hang&Go kits for hyperthermic perfusion procedures are most at risk. Patients receiving these treatments may be affected if the kits are not sterile.
Check the lot numbers on your Hang&Go kit: F180266, F180315, or F190169. The kits were sold with Reference Code R9900120.
Identify your kit's lot number from the list: F180266, F180315, or F190169.
The sterilization contractor reported that some lots may not be sterile, which could lead to infection risks during medical procedures.
Check the lot number on your kit; affected lots are F180266, F180315, or F190169.
Contact RanD directly for guidance on next steps, as the recall remedy is not specified in the record.
We’ve drafted a message you can send RanD to request your refund or repair — edit it as you like.
Subject: Recall Z-2048-2021 — RanD RanD Hello, I own a RanD that is covered by recall Z-2048-2021 from RanD. 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.
