Busse Hospital Disposables 8563Recalls & reported problems
Robert Busse & CO., Inc. · Spine Injection Tray · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Recalls naming this device
- Oct 21, 2022Class IIOpen, Classified
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
Z-0326-2023 · Root cause: Device Design · Recall details · FDA record ↗
Other Nerve Block Tray devices
- Medline Industries, Inc. PAIN1622AMedline Industries, Inc. · Nerve block tray2 recalls0 reports
- Medline Industries, Inc. PAIN0150CMedline Industries, Inc. · Nerve block tray2 recalls0 reports
- Busse Hospital Disposables 8561Robert Busse & CO., Inc. · Nerve Block Tray2 recalls0 reports
- Medline Industries, Inc. DYNJRA1860Medline Industries, Inc. · Nerve block tray2 recalls0 reports
- Medline Industries, Inc. DYNJ42367BMedline Industries, Inc. · Nerve block tray2 recalls0 reports
- Medline Industries, Inc. DYNJRA1590Medline Industries, Inc. · Nerve block tray1 recall1 report
- Medline Industries, Inc. DYNJ0703127AMedline Industries, Inc. · Nerve block tray1 recall0 reports
- Busse Hospital Disposables 6259R1Robert Busse & CO., Inc. · Nerve Block Tray1 recall0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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