Recall archive / FDA device enforcement
Busse JOINT INJECTION TRAY -Intended as a nerve block REF No. 8561 R1 — FDA record Z-0325-2023
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Oct 21, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Busse JOINT INJECTION TRAY -Intended as a nerve block REF No. 8561 R1
- 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
- Classification
- Class II
- Recalling firm
- Busse Hospital Disposables, Inc.
- Quantity
- 80 cases
- Agency-reported status
- Ongoing
- Source record identifier
- Z-0325-2023
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | UDI-DI: (01)00849233016712 Lot Number: 2230276 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
TX
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Dec 7, 2022
- Recall initiation date
- Oct 21, 2022
- Center classification date
- Nov 29, 2022
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.