Stradis Healthcare recalls single shot epidural kits with possible sterility breaches. Affected items have specific serial numbers and item numbers. Consumers should contact the manufacturer for details.
Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in the sterility of the kit.
Stradis Healthcare is recalling single-shot epidural kits that may have an incomplete seal on the outer bag, risking a breach in sterility. This could lead to infections during medical procedures if the kit is used without proper sterility.
The outer bag may not seal properly during manufacturing, which could allow contamination. If the kit is used without sterility, it might cause infections during medical procedures.
Healthcare professionals using the recalled single-shot epidural kits for medical procedures are most at risk. Patients receiving these kits during surgery may also be affected.
Check for item number 570-3089 on the kit. Look for serial numbers starting with 22251491690 or UDI/DI codes H65857030891 and M75257030890.
Identify the item number (570-3089), serial numbers starting with 22251491690, or UDI/DI codes H65857030891 and M75257030890.
The item number is 570-3089.
Check for serial numbers starting with 22251491690 or UDI/DI codes H65857030891 and M75257030890.
The recall does not specify a remedy, so contact Stradis Healthcare directly for instructions.
We’ve drafted a message you can send Stradis Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0530-2023 — Stradis Healthcare Stradis Healthcare Hello, I own a Stradis Healthcare that is covered by recall Z-0530-2023 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.
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.