Home/Recalls/FDA-Z-1781-2026
FDA DevicesClass II

COOK MEDICAL Ciaglia Blue Rhino Percutaneous Tracheostomy Introducer Set: Refer...

Published: April 15, 2026Recall ID: Z-1781-2026Category: devicesCountry: US

Reason for Recall / Hazard

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Product Description & Identification

COOK MEDICAL Ciaglia Blue Rhino Percutaneous Tracheostomy Introducer Set: Reference Part Number C-PTIS-100-FLEX-HC, Order Number G32092; Reference Part Number C-PTIS-100-HC, Order Number G12115.

Affected Products

COOK MEDICAL Ciaglia Blue Rhino Percutaneous Tracheostomy Introducer Set: Reference Part Number C-PTIS-100-FLEX-HC, Order Number G32092; Reference Part Number C-PTIS-100-HC, Order Number G12115.

Additional Source Details

FieldValue
CityBloomington
StateIN
Event id98495
Address 1750 N Daniels Way
Code infoReference Part Number C-PTIS-100-FLEX-HC, UDI (01)00827002320925(17)270812(10)NS16200246, Lot Number NS16200246; Reference Part Number C-PTIS-100-FLEX-HC, UDI (01)00827002320925(17)270803(10)NS16189601, Lot Number NS16189601; Reference Part Number C-PTIS-100-FLEX-HC, UDI (01)00827002320925(17)270827(10)NS16226797, Lot Number NS16226797; Reference Part Number C-PTIS-100-FLEX-HC, UDI (01)00827002320925(17)270812(10)NS16200247, Lot Number NS16200247; Reference Part Number C-PTIS-100-FLEX-HC, UDI (01)00827002320925(17)270803(10)NS16189598, Lot Number NS16189598; Reference Part Number C-PTIS-100-FLEX-HC, UDI (01)00827002320925(17)270803(10)NS16189586, Lot Number NS16189586; Reference Part Number C-PTIS-100-FLEX-HC, UDI (01)00827002320925(17)270803(10)NS16189600, Lot Number NS16189600; Reference Part Number C-PTIS-100-FLEX-HC, UDI (01)00827002320925(17)270620(10)16120672, Lot Number 16120672; Reference Part Number C-PTIS-100-FLEX-HC, UDI (01)00827002320925(17)270803(10)NS16189607, Lo... [TRUNCATED]
Postal code47404-9120
Report date20260415
Product typeDevices
Product quantity484 units
Reason for recallProducts from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260305
Initial firm notificationTwo or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date20260406

Overview

  • Recalling FirmCook Incorporated
  • StatusOngoing
  • Risk LevelClass II
  • DistributionWorldwide distribution.
Official Agency Alert