The Recall Desk
SevereFDA (Devices)·Z-0605-2021·Announced 2020-12-30

Cook Inc. Recalls Flexor Check-Flo Introducers Due to Separation Risk

Cook Inc. is recalling Flexor Check-Flo Introducers because the sheath may separate during use, posing a risk of life-threatening adverse events.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The source text explicitly states that the defect could result in 'life-threatening adverse events' including embolization and hemorrhage, which aligns with the rubric criteria for Severe (4) involving significant injury reports or high-risk structural defects in medical devices.

Plain-English summary

Cook Inc. is recalling 1,152 units of Flexor Check-Flo Introducers, model RPN KCFW-7.0-35-70-RB-HFANL1-HC, Order Number G56227. These medical devices are intended to introduce therapeutic or diagnostic devices into the vasculature, excluding coronary and neuro vasculature.

The recall is due to an increased likelihood of the introducer sheath separating at the proximal bond site. If separation occurs during use, it could result in life-threatening adverse events. Potential adverse events include increased procedural time, intervention to retrieve a separated segment, embolization occluding blood flow to a vital organ, vessel injury, and hemorrhage.

The affected units were distributed nationwide in the United States and globally to numerous countries including Australia, Singapore, and various nations in Europe, Asia, and the Middle East. Specific lot numbers are listed in the agency's recall record. Healthcare facilities and distributors should stop using these devices and contact Cook Inc. for further instructions.

The recalled product

Product
Flexor Check-Flo Introducer, RPN KCFW-7.0-35-70-RB-HFANL1-HC, Order Number G56227 Flexor Introducers and Guiding Sheaths are intended to introduce therapeutic or diagnostic devices into the vasculature, excluding coronary and neuro vasculature.
Manufacturer
Cook Inc.
Category
Medical Device — Vascular Introducer
Hazard
Affected units
1,152

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (20)

  • Lot Numbers: 13189185
  • 13194984
  • 13202958
  • 13205307
  • 13207466
  • 13207473
  • 13231809
  • 13234793
  • 13249454
  • 13262331
  • 13268033
  • 13288117
  • 13303369
  • 13303376
  • 13315174
  • 13332151
  • 13337783
  • 13337797
  • 13346088
  • 13346089

Distribution

Distributed nationwide across the United States.

The notice also names 51 states specifically:

Part of a larger recall action

This product is one of 21 recalled by Cook Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 21 products in this recall →

Related recalls

Same manufacturer · Cook Inc.

See all →

Same hazard · device separation

See all →