Lifeguard LG-20-150Recalls & reported problems
Navilyst Medical, Inc. · LIFEGUARD Safety Needle · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI H787LG201505), received between Feb 7, 2023 and Feb 7, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (2 reports).
3 other recalls cover devices cleared under the same FDA submission (K013871); they may or may not involve this specific model.
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.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
- Detachment of Device or Device Component2
- Device Damaged Prior to Use2
- Difficult to Advance2
- Difficult to Remove2
- Dull, Blunt2
- Failure to Advance2
- Fracture2
Patient problems
- Needle Stick/Puncture2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 7, 2023Fracture; Material Frayed; Material Puncture/Hole; Difficult to Remove; Material Perforation; Device Damaged Prior to Use; Dull, Blunt; Failure to Advance; Detachment of Device or Device Component; Difficult to Advance; Material Twisted/Bent; Adverse Event Without Identified Device or Use Problem; No Apparent Adverse Event; Fracture; Material Frayed; Material Puncture/Hole; Difficult to Remove; Material Perforation; Device Damaged Prior to Use; Dull, Blunt; Failure to Advance; Detachment of Device or Device Component; Difficult to Advance; Material Twisted/Bent; Adverse Event Without Identified Device or Use Problem; No Apparent Adverse Event
AN END USER REPORTED AN EVENT WHEN USING A LG 20GA X 1.5IN W/O Y-SITE KIT. IT WAS REPORTED THAT THERE WAS A MALFUNCTION OF THE SAFETY LOCKING SYSTEM IN A PROCEDURE. THE FOLLOWING WAS REPORTED: AFTER ENGAGING THE SAFETY, AFTER USAGE IN A PROCEDURE, THE NURSE INSPECTED THE SAFETY DUE TO THE PREVIOUS DAY'S INCIDENT AS A PRECAUTION. IT WAS NOTICED THE NEEDLE DID NOT ENGAGE IN THE SAFETY. THE NURSE WAS PUNCTURED BY THE NEEDLE ENOUGH TO DRAW BLOOD. SHE HAD TO HAVE LAB WORK DONE ALONG WITH THE PATIENT PER THE FACILITY'S PROTOCOL.
Patient problems: Needle Stick/Puncture
MAUDE report 16311731 ↗MalfunctionFeb 7, 2023Fracture; Material Frayed; Material Puncture/Hole; Difficult to Remove; Material Perforation; Device Damaged Prior to Use; Dull, Blunt; Failure to Advance; Detachment of Device or Device Component; Difficult to Advance; Material Twisted/Bent; Adverse Event Without Identified Device or Use Problem; No Apparent Adverse Event; Fracture; Material Frayed; Material Puncture/Hole; Difficult to Remove; Material Perforation; Device Damaged Prior to Use; Dull, Blunt; Failure to Advance; Detachment of Device or Device Component; Difficult to Advance; Material Twisted/Bent; Adverse Event Without Identified Device or Use Problem; No Apparent Adverse Event
AN END USER REPORTED AN EVENT WHEN USING A LG 20GA X 1.5IN W/O Y-SITE KIT. IT WAS REPORTED THAT THERE WAS A MALFUNCTION OF THE SAFETY LOCKING SYSTEM IN A PROCEDURE. THE NURSE REPORTING THE EVENT STATED THAT AFTER THE DEVICE WAS USED IN THE PROCEDURE, THE SAFETY WAS ENGAGED ON THE NEEDLE. SHE PICKED UP THE DEVICE AND WAS PUTTING IT INTO THE BIOHAZARD CONTAINER WHEN HER THUMB WAS STUCK BY THE PORT NEEDLE THAT WAS STICKING OUT OF THE TOP END OF THE YELLOW SAFETY CAP. THE NURSE THAT WAS STUCK WITH THE USED NEEDLE DID HAVE TO GO THROUGH ADDITIONAL LAB TESTING PER OUR PROTOCOL.
Patient problems: Needle Stick/Puncture
MAUDE report 16311730 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K013871. One submission often covers many models, so check the product and lot details in each record.
- Z-0679-2018 · Jul 24, 2017 · Terminated20Ga x .75 LifeGuard Huber Needle with Y-site. Product Code: CLGY-2034.
- Z-0914-2013 · Jan 21, 2013 · TerminatedLifeguard Infusion Set with Smartsite, 20Ga, 1, CLGY-2010 Huber type needle set used for the infusion of medical fluids into implantable ports.
- Z-1327-2011 · Nov 16, 2010 · TerminatedChurchill Medical Systems LifeGuard Non-Coring Huber Needle, Lifeguard Non-Coring Safety Infusion Set 22GA, 3/4"; Item # CLG-2234 The Lifeguard
Other Set, administration, intravascular devices
- Autosoft XC 1001680Unomedical A/S · Set, Administration, Intravascular1 death16,105 reports
- Autosoft90™ 1002817Unomedical A/S · Set, Administration, Intravascular1 recall11,907 reports
- Minimed™ Quick-set™ MMT-399AUnomedical A/S · Set, Administration, Intravascular9 deaths8,669 reports
- Medtronic Extended MMT-431AUnomedical A/S · Set, Administration, Intravascular3 deaths8,574 reports
- MiniMed™ Mio™ Advance MMT-242AUnomedical A/S · Set, Administration, Intravascular15 deaths8,164 reports
- CADD 21-7302-24Icu Medical, Inc. · Set, administration, intravascular4 recalls1 death4,657 reports
- Autosoft XC 1001681Unomedical A/S · Set, Administration, Intravascular1 death4,216 reports
- Minimed™ Quick-set™ MMT-397AUnomedical A/S · Set, Administration, Intravascular19 deaths4,134 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 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- 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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