Busse Hospital Disposables recalls sterile epidural trays with catalog number 6259R2 due to uncertain drug validation methods. Affected lots include 2130839, 2131167, 2131230, and 2131210. Consumers should check their product details.
Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufacture the drug products
Busse Hospital Disposables is recalling sterile epidural trays with catalog number 6259R2 because the drug products inside may not be properly validated. This could affect medical safety during epidural procedures.
The recall is due to uncertainty about whether the drug products in the swab/swabstick kits were properly validated during manufacturing. This could lead to potential safety issues during medical procedures.
Healthcare professionals using these trays for epidural procedures are most at risk. Patients receiving epidural treatments with the recalled trays may be affected.
Check for catalog number 6259R2 on the tray. Affected lots include 2130839, 2131167, 2131230, and 2131210. The UDI is 00849233000278.
Look for catalog number 6259R2 and affected lot numbers (2130839, 2131167, 2131230, 2131210) on the tray.
The recall is due to uncertainty about the adequacy of validation methods used to manufacture the drug products in the swab/swabstick kits.
Check the product details to see if it matches the recalled catalog number and lot numbers. If it does, contact Busse Hospital Disposables for further instructions.
The recall is for potential safety concerns related to the drug products, but specific risks are not clearly described in the notice.
We’ve drafted a message you can send Busse Hospital Disposables to request your refund or repair — edit it as you like.
Subject: Recall Z-1170-2022 — Busse Hospital Disposables Busse Hospital Disposables Hello, I own a Busse Hospital Disposables that is covered by recall Z-1170-2022 from Busse Hospital Disposables. 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.
