Cook G02464Recalls & reported problems
Cook Incorporated · Vinyl Connecting Tube · Class 1
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
- Aug 16, 2022Open, Classified
Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.
Z-1844-2022 · Root cause: Under Investigation by firm · FDA record ↗
Other CONNECTOR, CATHETER devices
- Cook G02278Cook Incorporated · CONNECTOR, CATHETER1 recall7 reports
- Cook G02791Cook Incorporated · CONNECTOR, CATHETER1 recall2 reports
- Medline DYND12200Medline Industries, Inc. · CONNECTOR, CATHETER1 recall2 reports
- Cook G02327Cook Incorporated · CONNECTOR, CATHETER1 recall1 report
- CARDINAL HEALTH SU130-4601Cardinal Health 200, LLC · CONNECTOR, CATHETER1 recall0 reports
- Cook G02898Cook Incorporated · CONNECTOR, CATHETER1 recall0 reports
- Medline DYND2219Medline Industries, Inc. · CONNECTOR, CATHETER1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.