CARDINAL HEALTH SNEX4VSSSBRecalls & reported problems
Cardinal Health 200, LLC · SHY VP SHUNT PACK · Class N
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
- Jul 14, 2026Class IIOpen, Classified
Cardinal Health was recently informed of a medical device recall from MEDICOM concerning the Ritmed Neurological Sponges. The recall is being issued due to unexpected variability of endotoxin levels on the products.
Z-2947-2026 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Other Aid, visual, for nausea devices
- CARDINAL HEALTH SEN48SNST6Cardinal Health 200, LLC · Aid, visual, for nausea1 recall0 reports
- CARDINAL HEALTH SNE51LMK10Cardinal Health 200, LLC · Aid, visual, for nausea1 recall0 reports
- CARDINAL HEALTH SNE81ACA14Cardinal Health 200, LLC · Aid, visual, for nausea1 recall0 reports
- CARDINAL HEALTH SEN54ENUPACardinal Health 200, LLC · Aid, visual, for nausea1 recall0 reports
- CARDINAL HEALTH SEN43NLANACardinal Health 200, LLC · Aid, visual, for nausea1 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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