Pulset 3373-91Recalls & reported problems
Westmed, Inc. · Full Kit, Pulset 3cc Syringe 23g x 1" (.6 x 25mm) safety Tip 25u Balanced Heparin · Class 1
- 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 8, 2022Terminated
The kits are being recalled due to a lack of sterility of a spare needle contained within the kits. There is a potential for skin infection or sepsis if the patient is exposed to a non-sterilized, unused needle.
Z-1779-2022 · Root cause: Process control · FDA record ↗
Other Arterial Blood Sampling Kit devices
- MEDLINE ART995Medline Industries, Inc. · Arterial blood sampling kit4 recalls0 reports
- MEDLINE ART1070AMedline Industries, Inc. · Arterial blood sampling kit3 recalls0 reports
- MEDLINE ART775BMedline Industries, Inc. · Arterial blood sampling kit2 recalls0 reports
- Centurion ART155ACenturion Medical Products Corporation · Arterial blood sampling kit2 recalls0 reports
- MEDLINE ART890AMedline Industries, Inc. · Arterial blood sampling kit2 recalls0 reports
- OTHER P42453Medline Industries, Inc. · Arterial blood sampling kit2 recalls0 reports
- MEDLINE ART1180Medline Industries, Inc. · Arterial blood sampling kit2 recalls0 reports
- MEDLINE ART1160Medline Industries, Inc. · Arterial blood sampling kit2 recalls0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.