CARDINAL HEALTH PGVMDVB28Recalls & reported problems
Cardinal Health 200, LLC · KIT,GU DAVINCI · Class 2
Data updated Oct 16, 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 16, 2026.
Recalls naming this device
- Aug 18, 2026Open, Classified
The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece that can pool on the floor. The impact can range from user dissatisfaction to the potential for the user of slip and fall.
Z-3296-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Other Endoscope introducer kit devices
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- Medline Industries, Inc. DYNJ44673GMedline Industries, Inc. · Endoscope introducer kit2 recalls0 reports
- Medline Industries, Inc. DYNJ66447Medline Industries, Inc. · Endoscope introducer kit2 recalls0 reports
- Merit Medical® 00884450360408Merit Medical Systems, Inc. · Endoscope introducer kit1 recall0 reports
- CARDINAL HEALTH SEN15SERM5Cardinal Health 200, LLC · Endoscope introducer kit1 recall0 reports
- CARDINAL HEALTH PGVMDVB26Cardinal Health 200, LLC · Endoscope introducer kit1 recall0 reports
- CARDINAL HEALTH SBA73CLK26Cardinal Health 200, LLC · Endoscope introducer kit1 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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