Busse Hospital Disposables recalls Universal Nerve Block Tray (Catalog 9818) due to uncertain drug validation methods. Affected units include specific lot numbers. 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 Universal Nerve Block Trays with catalog number 9818 because the drug products inside may not have been properly validated during manufacturing. This could affect medical safety if used improperly.
The recall is due to uncertainty about whether the drug products in the trays were correctly validated during manufacturing. This means the safety of the drugs could be compromised, potentially leading to medical risks if used.
Healthcare professionals using the Universal Nerve Block Tray for medical procedures are most at risk. Patients receiving treatments with these trays may also be affected if the drug products are unsafe.
Check for the catalog number 9818 on the Universal Nerve Block Tray. Affected units include specific lot numbers: 2030783, 2031093, 2130287, 2130412, 2130681, 2131043.
Reach out to Busse Hospital Disposables for specific guidance on the recalled units.
The recall is due to uncertainty about the adequacy of validation methods used to manufacture the drug products in the trays.
Lot numbers 2030783, 2031093, 2130287, 2130412, 2130681, and 2131043 are affected.
Check for catalog number 9818 and the specific lot numbers listed in the recall 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-1162-2022 — Busse Hospital Disposables Busse Hospital Disposables Hello, I own a Busse Hospital Disposables that is covered by recall Z-1162-2022 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.
