Busse Hospital Disposables recalls Nerve Block Tray Catalog 934: drug products may have manufacturing validation issues. Affected units include specific lot numbers. 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 Nerve Block Trays with catalog number 9342 due to potential manufacturing validation issues with the drug products inside. This could affect the safety and reliability of the drug products used in nerve block procedures.
The drug products in these trays may not be manufactured with validated test methods, which could lead to safety concerns. This uncertainty affects the reliability of the drug products during medical procedures.
Healthcare professionals using the Nerve Block Tray for nerve block procedures are most at risk. Patients receiving these procedures may also be affected if the drug products are used incorrectly.
Check for the catalog number 9342 on the Nerve Block Tray. Lot numbers 2031019S and 2130222S are affected. The unique device identifier (UDI) 00849233009073 is also associated with this recall.
Reach out to Busse Hospital Disposables for specific instructions on handling the recalled product.
The catalog number is 9342.
Lot numbers 2031019S and 2130222S are affected.
The UDI is 00849233009073.
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-1160-2022 — Busse Hospital Disposables Busse Hospital Disposables Hello, I own a Busse Hospital Disposables that is covered by recall Z-1160-2022 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.
