ARROW IPN922633Recalls & reported problems
Teleflex Incorporated · Arrowg+ard Blue(R) PSI Kit for use with 7.5 - 8 Fr. Catheters · Class 2
All models of ARROW (1494)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10801902202335), received between Jan 16, 2024 and Jan 16, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Gas/Air Leak” (1 report).
17 other recalls cover devices cleared under the same FDA submission (K780532); 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Gas/Air Leak1
- Material Puncture/Hole1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 16, 2024Material Puncture/Hole; Gas/Air Leak; Material Puncture/Hole; Gas/Air Leak
IT WAS REPORTED THAT: CATHETER WAS IN PATIENT. WHEN THE NURSE WAS PULLING BACK FOR BLOOD, AIR WAS COMING OUT. LINE WAS REMOVED AND FOUND TO HAVE A HOLE. I HAVE THE EQUIPMENT SAVED. ADDITIONAL INFORMATION. THE NURSE REMOVED THE LINE AS SOON AS THE ISSUE WAS IDENTIFIED. THERE WAS NO REPORTED PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18516052 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K780532. One submission often covers many models, so check the product and lot details in each record.
- Z-2385-2026 · Apr 21, 2026 · Open, ClassifiedDescription/REF: ACCESS TRAY/GU-04020; PSI KIT: 8.5 FR/AK-09803-CDC; PSI KIT: 9 FR/AK-09903-CDC; PSI KIT: 8.5 FR X 4 IN (10 CM)/ASK-09810-PCMH1; PSI KIT: 9 FR X 10 CM/ASK-09903-KH;
- Z-1242-2020 · Dec 20, 2019 · TerminatedArrow PSI Kit for use with 7 - 7.5 Fr. Catheters ASK-09801-UPM
- Z-2576-2018 · May 23, 2018 · TerminatedPercutaneous Sheath Introducer Kit for use with 7 - 7.5 Fr. Catheters (8 Fr. 10 cm sheath length .035 inch dia. spring-wire guide), REF ES-09807. The percutaneous sheath introduc
- Z-2011-2018 · Apr 11, 2018 · TerminatedSpring-Wire Guide Introducer Catheter Assembly; Product Code: CN-04018
- Z-2032-2018 · Apr 11, 2018 · Terminated9 Fr. Radiopaque Polyurethane Sheath/Dilator with Integral Hemostasis Valve/Side Port for use with 7 - 8 Fr. Catheters and Arrow Percutaneous Introducer System; Product codes: SS-0
- Z-1977-2018 · Apr 11, 2018 · TerminatedPercutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port and Sharps Safety Features (Recommended for use with 7 Fr. Catheters); Product Code: ASK-09907-SB
- Z-2031-2018 · Apr 11, 2018 · TerminatedARROWg+ard Blue PSI Kit with Integral Hemostasis Valve/ Side Port for use with 7 - 7.5 Fr. Catheters; Product codes: SF-29803-1
- Z-1976-2018 · Apr 11, 2018 · TerminatedPercutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port for use with 7.5 - 8 Fr. Catheters; Product Code: ASK-09903-UPA
- Z-1329-2018 · Dec 22, 2017 · Terminated(1) Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port, Sharps Safety Features, and Maximal Barrier Precautions for use with 7.5 - 8 Fr. Catheters, Part Nu
- Z-1158-2018 · Nov 14, 2017 · TerminatedPercutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port, Sharps Safety Features and Maximal Barrier Precautions for use with 7.5 - 8 Fr. Catheters. Permits ven
- Z-1287-2018 · Oct 26, 2017 · TerminatedArterial Access Tray, introducer catheter; Model: GU-04020
- Z-2329-2017 · May 9, 2017 · Terminated1) Introducer Kit with Integral Hemostasis Valve/Side Port, Sharps Safety Features, and Maximal Barrier Precautions for use with 7.5 - 8 Fr., Introducer Catheter 2) Arrow PSI Kit
- Z-0066-2015 · Aug 6, 2014 · TerminatedArrow Select Kits (ASK) and Maximal Barrier Precautions Kits (CDC) with BD Medical Posiflush 10mL Saline Flush Syringe.
- Z-1713-2014 · Apr 14, 2014 · TerminatedArrow Percutaneous Sheath Introducer Kits The Percutaneous sheath introducer products permit venous or arterial access and device introduction to the central circulation.
- Z-0468-2014 · Oct 9, 2013 · TerminatedArrow Transradial Artery Access products Arrow Transradial Artery Access products are used for percutaneous introduction of devices into the radial artery for diagnostic and thera
…and 2 more.
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- Swartz™ 407451St. Jude Medical, Inc. · INTRODUCER, CATHETER5 deaths728 reports
- Edwards eSheath+ Introducer set 914ESPEdwards Lifesciences LLC · Introducer, Catheter22 deaths532 reports
- Fast-Cath™ 406849St. Jude Medical, Inc. · INTRODUCER, CATHETER420 reports
- VIZIGO D138503Biosense Webster Inc · INTRODUCER, CATHETER362 reports
- Agilis™ G408318St. Jude Medical, Inc. · INTRODUCER, CATHETER333 reports
- Agilis™ NxT Steerable Introducer Dual-Reach™ SI-1371-MSt. Jude Medical, Inc. · Introducer, catheter1 death301 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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