FDA Medical Device Recalls (openFDA)
Covidien: COVIDIEN Shiley Lo-Pro Oral/Nasal Tracheal Tube Cuffed REF 86051 7.0 mm I.D. The Shiley Lo-Pro Oral/Nasal Tracheal Tube Cuffed are indicated for airway management by oral/nasal intubation of the trachea for anesthesia or other short-term procedures.
- Recall number
- Z-1318-2023
- Recalling firm
- Covidien
- Product
- COVIDIEN Shiley Lo-Pro Oral/Nasal Tracheal Tube Cuffed REF 86051 7.0 mm I.D. The Shiley Lo-Pro Oral/Nasal Tracheal Tube Cuffed are indicated for airway management by oral/nasal intubation of the trachea for anesthesia or other short-term procedures.
- Status
- Open, Classified
- Initiated
- 2023-02-10
- Posted
- 2023-04-01
- Terminated
- not on file
- Reason
- Due to potential leaks associate with the Oral/Nasal Tracheal Tube Cuffed inflation system.
- Root cause
- Process control
- Action
- On 02/10/2023, Medtronic issued an "Urgent Medical Device Recall" letter via UPS 2 day delivery to customers informing them of potential cuff leaks from the device inflation system in Shiley Lo-Pro Oral/Nasal Tracheal Tube Cuffed. Customer are instructed to: 1. Quarantine all unused product from the affected lots of Shiley" Lo-Pro Oral/Nasal Tracheal Tube Cuffed. See attachment A for guidance on identifying potentially affected devices. 2. Return all unused product from the affected lots in their inventory to Medtronic as described on the Customer Confirmation Form. 3. Complete the enclosed Customer Acknowledgment Form even if they do not have unused inventory. 4. Pass on the notice to all those who need to be aware within their organization or to any organization where the potentially affected product from the specified lots has been transferred or distributed. Additional Information for Patient Management: As stated in the Instructions for Use that accompanies each device, each tube s cuff should be tested by inflation prior to use. Use of a device with this potential manufacturing assembly error may result in a delay to treatment while an alternate device is obtained. There are no additional patient management recommendations that should be employed for patients where potentially affected devices are currently in use or were used. These patients should be monitored in accordance with your medical facility s critical care protocols. Clinical staff should appropriately assess and manage patients for any adverse clinical outcomes. For questions or further assistance, contact a Medtronic Representative or Customer Service at 800-962-9888.
- Quantity
- 12,310 devices
- Distribution
- U.S.: AK, AZ, CA, FL, GA, IA, IL, IN, KS MD, MI, MS, NC, NE, NJ, NY, OH, OK, PA, SC, TX, UT, VA, WA, and WV O.U.S.: Canada
- Lot, serial or model codes
- Product Number: 86051 UDI-DI (GTIN) Code: 60884522000241 Lot Numbers: 22G0343JZX 22G0344JZX
- 510(k) numbers
- ["K871204"]
- PMA numbers
- not on file
- Product code
- BTR
- Firm FEI
- 2936999
- Firm city
- Boulder
- Firm state
- CO
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28