Busse Hospital Disposables recalls Nerve Block Tray (Catalog 8415) due to uncertain drug validation. Affected lots include 2030832, 2031190, 2130252, 2130629, 2130742, 2131125, 2131223. No remedy specified.
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 Tray Catalog Number 8415 because drug manufacturing validation methods may be inadequate. This could affect patient safety during medical procedures.
The drug products in the tray were manufactured using test methods that may not have been properly validated. This uncertainty could lead to ineffective or unsafe drug delivery during medical procedures.
Healthcare providers using the Nerve Block Tray for medical procedures are most at risk. Patients receiving the drug products may also be affected.
Check for Catalog Number 8415 on the tray. Lot numbers 2030832, 2031190, 2130252, 2130629, 2130742, 2131125, or 2131223 are affected. The UDI code 00849233016811 is also associated with this recall.
Identify the Catalog Number and Lot Numbers on the Nerve Block Tray to confirm if it is affected.
The drug products in the tray were manufactured using test methods that may not have been properly validated, potentially affecting safety.
The recall record does not specify a remedy, so check the product details to see if it is affected.
Lot numbers 2030832, 2031190, 2130252, 2130629, 2130742, 2131125, and 2131223 are affected.
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-1158-2022 — Busse Hospital Disposables Busse Hospital Disposables Hello, I own a Busse Hospital Disposables that is covered by recall Z-1158-2022 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.
