FDA Device recall Z-0326-2023
Busse SPINE INJECTION TRAY-Intended as a nerve block REF No. 8563R1
- FDA Device
- Class II
- ongoing
- Published 2022-12-07
On 2022-12-07 the FDA classified a Class II recall of Busse SPINE INJECTION TRAY-Intended as a nerve block REF No. 8563R1 by Busse Hospital Disposables, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0326-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-10-21 |
| Published | 2022-12-07 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Busse Hospital Disposables |
| Distribution | TX |
Product
Busse SPINE INJECTION TRAY-Intended as a nerve block REF No. 8563R1
Reason
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
Identifiers
| code_info | UDI-DI: (01) 00849233016705 Lot Number: 2230458 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0326-2023%22
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