IV Administration Set 490062Recalls & reported problems
B. Braun Medical Inc. · NF1503 15 DR UNIV SPIKE,INJ SITE,BCV · Class 1
Data updated Oct 13, 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. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Oct 29, 2025Open, Classified
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
Z-0680-2026 · Root cause: Process control · FDA record ↗
Other ACCESSORIES, CATHETER devices
- Cook G00219Cook Incorporated · ACCESSORIES, CATHETER103 reports
- Discofix® 456020B. Braun Medical Inc. · ACCESSORIES, CATHETER60 reports
- Extension Set 456025B. Braun Medical Inc. · ACCESSORIES, CATHETER1 recall0 reports
- Centeze Centesis Catheter DRC-002-06Galt Medical Corp. · 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 13, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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