Busse Hospital Disposables recalls SPINE INJECTION TRAYs with adhesive liner that may damage product during use. Affected units have specific lot numbers and reference codes.
Kits containing 3M Steri-Drape Surgical Drapes recalled by 3M due to liner on the adhesive component is difficult to remove without damaging the product and may render the product unusable
Busse Hospital Disposables is recalling SPINE INJECTION TRAYs used for nerve blocks because the adhesive liner on the product can be difficult to remove without damaging it, potentially making the product unusable. This issue affects specific units with known lot numbers and reference codes.
The adhesive liner on the SPINE INJECTION TRAY can be difficult to remove without damaging the product. This may cause the tray to become unusable during nerve block procedures, potentially affecting treatment effectiveness.
Healthcare professionals using the SPINE INJECTION TRAY for nerve blocks are most likely affected. Patients receiving nerve blocks with this product may be at risk if the tray becomes unusable.
Check for the product name 'SPINE INJECTION TRAY' with reference code REF No. 8563R1. Affected units have lot number 2230458 and UDI-DI code (01) 00849233016705.
Verify the product name, reference code, and lot number to confirm if your unit is affected.
The adhesive liner on the SPINE INJECTION TRAY can be difficult to remove without damaging the product, potentially making it unusable during nerve block procedures.
The official recall notice does not specify a remedy or action for affected units.
Check for the product name 'SPINE INJECTION TRAY' with reference code REF No. 8563R1 and lot number 2230458.
We’ve drafted a message you can send Busse to request your refund or repair — edit it as you like.
Subject: Recall Z-0326-2023 — Busse Busse Hello, I own a Busse that is covered by recall Z-0326-2023 from Busse. 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.
