MEDLINE INDUSTRIES, INC. DYNJRA2633Recalls & reported problems
Medline Industries, Inc. · TRAY, 25G WHIT SPINAL W/PHARM · 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
- Apr 10, 2026Class IOpen, Classified
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.
Z-2232-2026 · Root cause: Component design/selection · Recall details · FDA record ↗
Other Spinal epidural anesthesia kit devices
- Medline Industries, Inc. DYNJRA9040Medline Industries, Inc. · Spinal epidural anesthesia kit2 recalls2 reports
- Medline Industries, Inc. DYNJ34418MMedline Industries, Inc. · Spinal epidural anesthesia kit2 recalls1 report
- Design Options® 530184B. Braun Medical Inc. · Spinal epidural anesthesia kit2 recalls1 report
- Design Options® 530159B. Braun Medical Inc. · Spinal epidural anesthesia kit2 recalls0 reports
- Medline Industries, Inc. DYNJ34418LMedline Industries, Inc. · Spinal epidural anesthesia kit2 recalls0 reports
- Medline Industries, Inc. DYNJRA1849Medline Industries, Inc. · Spinal epidural anesthesia kit2 recalls0 reports
- Medline Industries, Inc. DYNJRA1739BMedline Industries, Inc. · Spinal epidural anesthesia kit2 recalls0 reports
- Medline Industries, Inc. DYNJRA1739AMedline Industries, Inc. · Spinal epidural anesthesia kit2 recalls0 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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