Busse Hospital Disposables recalls MBB Tray catalog 9882 with lot numbers 2130220-2131063 due to uncertain drug test validation. 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 MBB Tray catalog number 988:2 with specific lot numbers because the drug products inside may not be made safely. This could affect people using these medical swabs.
The drug products in these swabs were made using test methods that weren't fully validated. This uncertainty means the products might not be safe for medical use, potentially causing harm.
People who own or use the MBB Tray catalog number 9882 with the listed lot numbers are affected. Medical users are most at risk due to potential safety issues with the drug products.
Check for catalog number 9882 on the MBB Tray. Look for lot numbers 2130220, 2130445, or 2131063. The unique device identifier (UDI) is 00849233000179.
Identify your MBB Tray's catalog number and lot numbers to confirm if it's recalled.
The drug products in these swabs were made using test methods that weren't fully validated, raising safety concerns.
The recall record doesn't specify a remedy, so check with Busse Hospital Disposables for further instructions.
Look for catalog number 9882 and lot numbers 2130220, 2130445, or 2131063 on the product.
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-1163-2022 — Busse Hospital Disposables Busse Hospital Disposables Hello, I own a Busse Hospital Disposables that is covered by recall Z-1163-2022 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.
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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.
