Busse Hospital Disposables recalls Port Tray Catalog 7607 swab kits due to uncertain drug test validation. Affected lots include 2010357, 2110129, 2110181, 2110225, 2110252. No specific action steps provided in recall notice.
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 Port Tray Catalog 7607 swab kits because the drug manufacturing process may not have been validated properly. This could affect the safety and effectiveness of the products.
The recall is due to uncertainty about whether the test methods used to manufacture the drug products were validated correctly. This could mean the products might not work as intended or could be unsafe for medical use.
Users of the Port Tray Catalog 7607 swab kits who purchased them between the listed lot numbers. Healthcare professionals and patients using these kits for medical purposes are most at risk.
Check the lot numbers on the product: 2010357, 2110129, 2110181, 2110225, or 2110252. The product is labeled as Port Tray Catalog 7607.
Look for lot numbers 2010357, 2110129, 2110181, 2110225, or 2110252 on the Port Tray Catalog 7607 swab kits.
The recall is due to uncertainty about whether the test methods used to manufacture the drug products were validated correctly.
The recall notice does not specify any action steps for affected products.
Yes, check for lot numbers 2010357, 2110129, 2110181, 2110225, or 2110252.
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-1156-2022 — Busse Hospital Disposables Busse Hospital Disposables Hello, I own a Busse Hospital Disposables that is covered by recall Z-1156-2022 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.
