LSL HEALTHCARE 2519CPRecalls & reported problems
LSL Industries, LLC · Central Line Dressing Kit · Class 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
- Dec 22, 2025Class IIOpen, Classified
BD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an open seal on the packaging of the applicators.
Z-1219-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Other Peripheral catheter insertion kit devices
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- VYGON AMS-7192CS-4Vygon Corporation · Peripheral catheter insertion kit1 recall0 reports
- MCI MCITX-1Vygon Corporation · Peripheral catheter insertion kit1 recall0 reports
- VYGON AMS-7063-1Vygon Corporation · Peripheral catheter insertion kit1 recall0 reports
- VYGON AMS-9093CPVygon Corporation · Peripheral catheter insertion kit1 recall0 reports
- VYGON AMS-8010CP-1Vygon Corporation · Peripheral catheter insertion kit1 recall0 reports
- CARDINAL HEALTH PVMHIVM14Cardinal Health 200, LLC · Peripheral catheter insertion kit1 recall0 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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