Busse Hospital Disposables recalls Single Shot Epidural Tray (Catalog 6183R1) due to uncertain drug validation. Affected lots include 2030967-2131248. Consumers should contact for 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 Single Shot Epidural Trays with specific catalog numbers because drug manufacturing validation methods may be uncertain. This could affect patient safety during epidural procedures.
The recall involves drug products in the tray that were manufactured using test methods not fully validated. This uncertainty could lead to improper drug dosing or safety issues during medical procedures.
Healthcare professionals using the Single Shot Epidural Tray for epidural procedures. Patients receiving epidural anesthesia may be at risk if the device is used with unverified drug products.
Check for Catalog Number 6183R1 on the tray. Affected lots include 2030967 through 2131248. The UDI code 00849233007857 is also associated with these items.
Look for Catalog Number 6183R1 and affected lot numbers (2030967-2131248) on the tray.
The drug products in the tray were manufactured using test methods that may not have been adequately validated, raising safety concerns.
The recall record does not specify a remedy or action steps. Contact Busse Hospital Disposables for further instructions.
Yes, affected lot numbers range from 2030967 to 2131248.
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-1169-2022 — Busse Hospital Disposables Busse Hospital Disposables Hello, I own a Busse Hospital Disposables that is covered by recall Z-1169-2022 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.
