Manometer, Spinal-Fluid
FDA adverse event reports and recall history for manometer, spinal-fluid (product code FMJ), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 411
- Deaths
- 1
- Injuries
- 11
- Malfunctions
- 399
Reports per year
Source: FDA adverse event reports by year received, 1999–2025. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
- 2004-11-24TerminatedOther
Portex Hypodermic Needle-Pro 5 ml Syringe, 20g x 1'' Needle Catalog Number: 4251
Sterility of the device is compromised due to packaging defects
- 2004-11-24TerminatedOther
Portex Hypodermic Needle-Pro 5 ml Syringe, 21g x 1 '' Needle Catalog Number: 4252
Sterility of the device is compromised due to packaging defects
- 2004-11-24TerminatedOther
Hypodermic Needle-Pro 5 ml Syringe, 21g x 1'' Needle Catatlog Number: 4253
Sterility of the device is compromised due to packaging defects
- 2004-11-24TerminatedOther
Portex Hypodermic Needle-Pro 5 ml Syringe, 22g x 1 '' Needle Catalog Number: 4254
Sterility of the device is compromised due to packaging defects
- TerminatedOther
Lumbar Tray Catalog 1091
Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufacture the drug products
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