Teleflex Medical Sheridan Preformed Cuffed Tracheal Tube, Nasal 6.5, Catalog Number: 5-22313, Teleflex Medical Ltd, Research Triangle Park, NC 27709 Used for oral or nasal intubation for airway management. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Sheridan Preformed Cuffed Tracheal Tube, Nasal 6.5, Catalog Number: 5-22313, Teleflex Medical Ltd, Research Triangle Park, NC 27709 Used for oral or nasal intubation for airway management.
Brand
Teleflex Medical
Lot Codes / Batch Numbers
Lot number 01A0900364
Products Sold
Lot number 01A0900364
Teleflex Medical is recalling Sheridan Preformed Cuffed Tracheal Tube, Nasal 6.5, Catalog Number: 5-22313, Teleflex Medical Ltd, R due to The Nasal Preformed Tracheal Tubes were found to have incorrect insertion depth mark printings.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The Nasal Preformed Tracheal Tubes were found to have incorrect insertion depth mark printings.
Recommended Action
Per FDA guidance
Consignees were notified by an Urgent Medical Device Recall letter on/about 07/06/2009. They were instructed to discontinue use of and return any of the recalled product to Teleflex Medical. Distributors were advised to forward the letter to their consignees to retrieve relevant product from those locations. A Recall Acknowledgement Form was attached to be returned to Teleflex Medical. Replacement product or credit will be provided to the consignee.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, FL, IL, KY, MA, NJ, NM, NC, OH, PA, RI, TN, TX, UT, VA, WA, WI
Page updated: Jan 10, 2026