Busse Hospital Disposables recalls IV Start Kit Catalog 8172 (lot numbers 2020561-2120911) due to uncertain drug validation methods. Consumers should contact the manufacturer 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 IV Start Kit Catalog 8172 because the drug products inside may not be manufactured with validated test methods. This could affect patient safety during medical procedures.
The recall is due to uncertainty about whether the test methods used to manufacture the drug products are adequate. This could lead to potential safety issues during medical procedures if the drug products are not validated correctly.
Healthcare professionals using the IV Start Kit for medical procedures are most at risk. Patients receiving treatments with this kit could be affected if the drug products are not properly validated.
Check for the IV Start Kit Catalog 8172 with lot numbers 2020561, 2020560, 2020650, 2120089, 2120018, 2120344, 2120442, 2120645, 2120768, or 2120911. The UDI is 00849233015883.
Reach out to Busse Hospital Disposables for specific instructions on handling the recalled product.
The recall is due to uncertainty about the adequacy of the test methods used to manufacture the drug products, which could affect patient safety.
Lot numbers 2020561, 2020560, 2020650, 2120089, 2120018, 2120344, 2120442, 2120645, 2120768, and 2120911.
Look for the IV Start Kit Catalog 8172 with the listed lot numbers or UDI 00849233015883.
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-1157-2022 — Busse Hospital Disposables Busse Hospital Disposables Hello, I own a Busse Hospital Disposables that is covered by recall Z-1157-2022 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.
