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CAREFLOW(TM) 1 LUMEN 3FR X 150MM

ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD. · Model 681640 · UDI-DI 00886333616404

FOZ Prescription
10
510(k) clearances
49,694
Adverse events (141 deaths)
394
Recalls
198
Facilities

Description

Kits Contents : Catheter 3FR OD 1.10mmx150mm; J guidewire OD 0.46mmx450mm, Steel Needle Introducer 22G OD 0.75mmx40mm; Floswitch(TM) Overneedle Introducer 20G OD 1.0mmx45mm, Dilator 4FR OD 1.27mm ID 0.51mm & Floswitch(TM).

Recalls

DateFirmReason
2026-03-11ARROW INTERNATIONAL, LLCDue to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
2026-03-05Cook IncorporatedProducts from the affected device lots were labeled with expiration dates that exceed the true shelf life.
2026-03-05Cook IncorporatedProducts from the affected device lots were labeled with expiration dates that exceed the true shelf life.
2026-03-05Cook IncorporatedProducts from the affected device lots were labeled with expiration dates that exceed the true shelf life.
2026-01-07Medline Industries, LPMedline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag
2026-01-07Medline Industries, LPMedline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag
2025-05-21Becton Dickinson Infusion Therapy Systems, Inc.Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
2025-05-21Becton Dickinson Infusion Therapy Systems, Inc.Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
2025-05-21Becton Dickinson Infusion Therapy Systems, Inc.Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.
2025-05-21Becton Dickinson Infusion Therapy Systems, Inc.Due to customer complaints, there is the possibility that catheter needle may be slow to retract or fail to retract.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.