Lower riskMedical device recall · FDA · Published October 21, 2022
Busse Joint Injection Tray Recall: Adhesive Liner May Cause Product Damage
Busse Hospital Disposables recalls joint injection trays with adhesive liner that may damage product. 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
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📍Recalling firmBusse Hospital Disposables, Inc.75 Arkay Dr · Hauppauge, NY 11788-3707
✎ GovInfoNow plain-language explainer
Busse Hospital Disposables is recalling joint injection trays intended for nerve blocks because the adhesive liner on the product can be difficult to remove without damaging it, potentially making the tray unusable. This affects specific lot numbers and reference codes. Read more at govinfonow.com/recall/59818-busse-joint-injection-tray-recall-adhesive-liner-may-cause-product.
“Busse Joint Injection Tray Recall: Adhesive Liner May Cause Product Damage.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/59818-busse-joint-injection-tray-recall-adhesive-liner-may-cause-product. Based on FDA recall #Z-0325-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0325-2023%22&limit=1).
The FDA announced on Oct. 21, 2022, that Busse Hospital Disposables, Inc. is recalling the Busse JOINT INJECTION TRAY due to a hazard involving difficult-to-remove liners. The agency issued recall number Z-0325-2023 for this Class II voluntary recall.
How to tell if you have it
Brand: Busse
Product: JOINT INJECTION TRAY -Intended as a nerve block REF No. 8561 R1
UPC: 00849233016712
Lot Number: 2230276
Distribution: TX
The hazard
The kits contain 3M Steri-Drape Surgical Drapes recalled by 3M because the liner on the adhesive component is difficult to remove without damaging the product. This damage may render the product unusable.
Context
GovInfoNow's records show Busse Hospital Disposables, Inc. has two other recalls on record since Feb. 22, 2022. Other recent recalls of similar products include Medline Nerve Block Tray 2 Kits Recall (Dec. 12, 2025) and Medline Nerve Block Trays Recall (April 27, 2026).
How to tell if you have this one
Check for the reference number 8561 R1 and lot number 2230276 on the product. The product is labeled as a joint injection tray intended for nerve blocks.
Brand
Busse
Product
Busse JOINT INJECTION TRAY
Category
Medical device
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Ongoing
Distribution
TX
Recall number
Product, codes & lots
Quantity
Z-0325-2023
Busse JOINT INJECTION TRAY -Intended as a nerve block REF No. 8561 R1; UDI-DI: (01)00849233016712 Lot Number: 2230276
80 cases
Z-0326-2023
Busse SPINE INJECTION TRAY-Intended as a nerve block REF No. 8563R1; UDI-DI: (01) 00849233016705 Lot Number: 2230458
40 cases
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for reference number 8561 R1 and lot number 2230276 on the tray.
Where it went and when
Where it was distributed
Distributed in Texas.
Listed by the agency
Not listed
FDA distribution: “TX” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Texas.
Recall timeline
FDA published this recall 47 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-0325-2023 (October 21, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0325-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.