Merit® Kit 00884450328613Recalls & reported problems
Merit Medical Systems, Inc. · Class 2
- 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.
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
- Sep 20, 2017Terminated
1 Cuff catheters were incorrectly configured and labeled as 2 Cuff product and placed into these dialysis kits.
Z-1145-2018 · Root cause: Mixed-up of materials/components · FDA record ↗
Other Dialysis administration kit devices
- Medical Action Industries 78791Medical Action Industries Inc. · Dialysis administration kit1 recall0 reports
- Medline Industries, Inc. DYNDC3088Medline Industries, Inc. · Dialysis administration kit1 recall0 reports
- Merit® Kit 00884450328620Merit Medical Systems, Inc. · Dialysis administration kit1 recall0 reports
- Medline Industries, Inc. DYNJ36932AMedline Industries, Inc. · Dialysis administration kit1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.