ARROW IPN919757Recalls & reported problems
Teleflex Incorporated · Radial Artery Catheterization · Class 2
All models of ARROW (1494)
Data updated Oct 16, 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.
32 other recalls cover devices cleared under the same FDA submission (K810675); 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.
Recalls naming this device
- Apr 21, 2026Open, Classified
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Z-2368-2026 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K810675. One submission often covers many models, so check the product and lot details in each record.
- Z-2397-2026 · Apr 21, 2026 · Open, ClassifiedDescription/REF: RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-1A; RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-X1A; ARTERIAL CATHETER KIT: 18 GA X 16 CM/ASK-04018-HCA; ARTERIAL CATHETER KIT: 18
- Z-3299-2024 · Jul 26, 2024 · Open, ClassifiedArrow Arterial Kits and Trays as follows: (1) Arrow Arterial Access Tray with 0.025" Spring-Wire Guide (Catheter Not Included), REF ASK-04001-BW1; (2) Arrow Arterial Access Tray
- Z-0844-2020 · Dec 12, 2019 · Open, ClassifiedArrow Arterial Catherization Kit-20 Ga. x 4.45 cm Radiopaque Polyurethane over 22 Ga. TW Introducer Needle with Integral .018" (0.46 mm) dia. Spring-Wire Guide Product Code: ASK-04
- Z-1969-2018 · Apr 11, 2018 · TerminatedArterial Line Kit with Sharps Safety Features and Maximal Barrier Precautions; Product Code: ASK-04018-OH1
- Z-1970-2018 · Apr 11, 2018 · TerminatedRadial Artery Catheterization Kit; Product Codes: ASK-04020-AH, ASK-04020-MIHS, ASK-04120-HF1
- Z-1972-2018 · Apr 11, 2018 · TerminatedRadial Artery Catheterization Kit with Sharps Safety Features; Product Codes: ASK-04020-RIHM
- Z-1971-2018 · Apr 11, 2018 · TerminatedArterial Catheterization Kit; Product Codes: ASK-04020-DH
- Z-2019-2018 · Apr 11, 2018 · TerminatedArterial Catheterization Kit; Product Code:NA-04550-1A
- Z-1968-2018 · Apr 11, 2018 · TerminatedRadial Arterial Access Kit; Product Code: ASK-04001-BID2
- Z-1330-2018 · Dec 22, 2017 · Terminated(1) Arterial Catheterization Kit, Part Number (PN): ASK-04018-CC; (2) Arterial Line Kit with Sharps Safety Features, PN: ASK-04510-HUM; (3) Arterial Line Kit with Sharps Safety Fea
- Z-1285-2018 · Oct 26, 2017 · TerminatedRadial Artery Catheterization Kit; Model: AK-04122
- Z-1283-2018 · Oct 26, 2017 · TerminatedRadial Artery Catheterization Kit; Model: AK-04020-C
- Z-1284-2018 · Oct 26, 2017 · TerminatedRadial Artery Catheterization Kit; Model: AK-04120
- Z-1281-2018 · Oct 26, 2017 · TerminatedRadial Artery Catheterization Kit; Model: AK-04018
- Z-1286-2018 · Oct 26, 2017 · TerminatedRadial Artery Catheterization Kit; Model: AK-04220
…and 17 more.
Other Wire, guide, catheter devices
- HI-TORQUE BALANCE MIDDLEWEIGHT UNIVERSAL II 1009664Abbott Vascular Inc. · WIRE, GUIDE, CATHETER321 reports
- SYNCHRO 14 M00313010Stryker Corporation · WIRE, GUIDE, CATHETER2 recalls220 reports
- PressureWire™ C12059Lightlab Imaging, Inc. · WIRE, GUIDE, CATHETER1 death296 reports
- SYNCHRO 2 M00326410Stryker Corporation · WIRE, GUIDE, CATHETER2 recalls155 reports
- ENROUTE .014" Guidewire 11686-01Silk Road Medical, Inc. · Wire, Guide, Catheter2 deaths228 reports
- ARROW IPN035915Teleflex Incorporated · WIRE, GUIDE, CATHETER217 reports
- OmniWire Pressure guide wire 89185Philips Image Guided Therapy Corporation · Wire, Guide, Catheter1 recall1 death160 reports
- ARROW IPN055780Teleflex Incorporated · Wire, guide, catheter4 recalls0 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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