Centeze Centesis Catheter DRC-002-06Recalls & reported problems
Galt Medical Corp. · Centeze Centesis Catheter · Class 1
All models of Centeze Centesis Catheter (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
- Mar 27, 2025Class IIOpen, Classified
Due to a potential open seal in the sterile barrier packaging .
Z-1731-2025 · Root cause: Process control · Recall details · FDA record ↗
Other Accessories, Catheter devices
- Cook G00219Cook Incorporated · ACCESSORIES, CATHETER103 reports
- Discofix® 456020B. Braun Medical Inc. · ACCESSORIES, CATHETER60 reports
- IV Administration Set 490062B. Braun Medical Inc. · ACCESSORIES, CATHETER1 recall0 reports
- Extension Set 456025B. Braun Medical Inc. · ACCESSORIES, CATHETER1 recall0 reports
- Centeze Centesis Catheter DRC-002-05Galt Medical Corp. · Accessories, Catheter1 recall0 reports
- Neff G10544Cook Incorporated · ACCESSORIES, CATHETER45 reports
- Cook G06299Cook Incorporated · ACCESSORIES, CATHETER18 reports
- Neff G08426Cook Incorporated · ACCESSORIES, CATHETER17 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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