Precision Delivery IV Extension Set PDB05CV1Recalls & reported problems
Quest Medical Inc · Class 2
All models of Precision Delivery IV Extension Set (3)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00634624921382), received between Oct 29, 2022 and Oct 29, 2022 — classified as 3 injuries.
The most frequently reported specific device problem is “Loss of or Failure to Bond” (3 reports).
1 other recall cover devices cleared under the same FDA submission (K202672); 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
- Loss of or Failure to Bond3
Patient problems
- Unspecified Infection3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryOct 29, 2022Loss of or Failure to Bond; Loss of or Failure to Bond
IT WAS REPORTED TO QUEST MEDICAL BY (B)(6) HOSPITAL OF (B)(6) OF AN ALLEGED ISSUE WITH PRECISION DELIVERY SETS. THE REPORT STATED THAT THE SET BONDING WAS ALLEGEDLY NOT HOLDING AND THAT THERE WAS AN INSTANCE OF BLOOD STREAM INFECTION.
Patient problems: Unspecified Infection
MAUDE report 15696430 ↗InjuryOct 29, 2022Loss of or Failure to Bond; Loss of or Failure to Bond
IT WAS REPORTED TO QUEST MEDICAL BY CHILDREN'S HOSPITAL OF BOSTON OF AN ALLEGED ISSUE WITH PRECISION DELIVERY SETS. THE REPORT STATED THAT THE SET BONDING WAS ALLEGEDLY NOT HOLDING AND THAT THERE WAS AN INSTANCE OF BLOOD STREAM INFECTION.
Patient problems: Unspecified Infection
MAUDE report 15696038 ↗InjuryOct 29, 2022Loss of or Failure to Bond; Loss of or Failure to Bond
IT WAS REPORTED TO QUEST MEDICAL BY CHILDREN'S HOSPITAL OF BOSTON OF AN ALLEGED ISSUE WITH PRECISION DELIVERY SETS. THE REPORT STATED THAT THE SET BONDING WAS ALLEGEDLY NOT HODLING AND THAT THERE WAS AN INSTANCE OF BLOOD STREAM INFECTION.
Patient problems: Unspecified Infection
MAUDE report 15695554 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K202672. One submission often covers many models, so check the product and lot details in each record.
- Z-1100-2023 · Dec 23, 2022 · Open, ClassifiedPrecision Delivery Set with Filter, REF: PD06F; and Precision Delivery Set with Trifurcated Luer, REF: PDT05CV2
Other Set, Administration, Intravascular devices
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- 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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