Recall Register

Device recall: Check-Flo Performer Introducer Set, Reference Part Number RCF-5.0-35-45-J, Order Number G27242. Performer Introducers…

Class II FDA enforcement event 95405. Recall start date: . Status in the FDA record: Ongoing.

Reason for recall, in the words of FDA

Cook Medical is conducting removal of a lot of Check-Flo Performer Introducer Set due to complaints that the white caps that connect the shaft to the hub of these products may disconnect.

Class II, in the words of FDA

a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote

Cook Incorporated started this device recall on 16 Sep 2024. The firm address in the FDA record is in Bloomington, IN. FDA put the recall in Class II. FDA event 95405 has 1 product record. The first FDA enforcement report date is 16 Oct 2024. The record gives the status Ongoing.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

International distribution to the country of Australia.

Recalling firm

Cook Incorporated, Bloomington, IN.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

1 product record in the event.

FDA event 95405: product records
Recall numberProductQuantityClassStatusReport date
Z-0045-2025Check-Flo Performer Introducer Set, Reference Part Number RCF-5.0-35-45-J, Order Number G27242. Performer Introducers are designed to perform as a guiding sheath and/or introducer sheath and come with a Check Flo valve.50 unitsClass IIOngoing16 Oct 2024

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class II: The middle of the three FDA recall classes.

The event in context

Device events that started in 2024
970
Share of these events in Class II
87%
Product records in this event
1Median of the firm: 2
Events of the firm on the register
16

Other events of the firm

Other FDA enforcement events of Cook Incorporated
InitiatedProduct (first record)TypeClassRecords
2 Apr 2026Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20 GPN G11916 Catheters for use in angiographic procedures are DeviceClass I3
5 Mar 2026COOK MEDICAL Approach CTO-6 Micro Wire Guide, Reference Part Number CMW-14-190-6G, Order Number G50786DeviceClass II18
26 Nov 2025Flexor Check-Flo Introducers and Sets, Reference Part Numbers: 1) KCFW-9.0-18/38-45-RB-ANL0-HC; 2) KCFW-9.0-18/38-45-RB-DeviceClass II3
15 May 2025Beacon Tip 5.0 Fr Angiographic catheters are designed to facilitate diagnostic and therapeutic procedures. Catheters areDeviceClass I1
17 Apr 2025Tornado Embolization Microcoil, intended for embolization of selective vessel supply to arteriovenous malformations and DeviceClass II1
17 Apr 2025Check=Flo Performer Introducer, 10.0Fr, Reference Part Number(RPN) REF RCFW-10.0-0-38-30-RB, Order Number (GPN) REF G086DeviceClass II2
14 Oct 2024Approach CTO Micro Wire Guide, RPN CMW-14-190-25G, GPN G50789DeviceClass II1
8 Oct 2024Approach CTO Micro Wire Guide, Guide Wire, Catalog Prefix CMW; Reference Part Numbers: CMW-14-190-12G CMW-14-190-18G CMWDeviceClass II2
15 May 2024Ultrathane Mac-Loc Locking Loop Multipurpose Drainage Catheter ULT16.0-38-25-P-6S-MCL-HC--Intended for percutaneous draiDeviceClass II2
1 Mar 2024Chiba Biopsy Needle - Used for aspiration biopsy. REFERENCE PART NUMBER (RPN) ORDER NUMBER (GPN): 1) DCHN-18-10.0 G01559DeviceClass II8

Cook Incorporated: all 16 events

Official channels

Cite this page

Recall Register. FDA enforcement event 95405. https://recallregister.com/fda/ii/95405/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA device enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: International distribution to the country of Australia.
What quantity of product is in FDA event 95405?
The FDA record gives this quantity: 50 units
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many device recalls of 2024 have the same class?
87% of the 970 device events that started in 2024 are in Class II.