Safe-T 4306CSPRecalls & reported problems
Carefusion 2200, Inc · Safe-T PLUS Adult Lumbar Puncture Tray - 22 G x 3 1/2 Inch Spinal Needle · Class 2
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. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Jan 20, 2022Open, Classified
Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Z-0797-2022 · Root cause: Process control · FDA record ↗
Other Lumbar puncture tray (adult & pediatric) devices
- N/A 4301CCarefusion 2200, Inc · Lumbar puncture tray (adult & pediatric)1 recall19 reports
- Safe-T 4301CSPCarefusion 2200, Inc · Lumbar puncture tray (adult & pediatric)1 recall7 reports
- Safe-T 4306CWSPCarefusion 2200, Inc · Lumbar puncture tray (adult & pediatric)1 recall7 reports
- N/A 4306CCarefusion 2200, Inc · Lumbar puncture tray (adult & pediatric)1 recall4 reports
- N/A 4304CCarefusion 2200, Inc · Lumbar puncture tray (adult & pediatric)1 recall1 report
- N/A 4306CWDFCarefusion 2200, Inc · Lumbar puncture tray (adult & pediatric)1 recall0 reports
- MEDLINE DYNJTS07025Medline Industries, Inc. · Lumbar puncture tray (adult & pediatric)1 recall0 reports
- N/A 4303CCarefusion 2200, Inc · Lumbar puncture tray (adult & pediatric)1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.