TELEFLEX MEDICAL INC Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is indicated to be used in any surgical procedure requiring attachment to a Chest Drainage device. The thoracic catheter is indicated for use less than 30 days. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is indicated to be used in any surgical procedure requiring attachment to a Chest Drainage device. The thoracic catheter is indicated for use less than 30 days.
Brand
TELEFLEX MEDICAL INC
Lot Codes / Batch Numbers
74K1900074 74K1901335 74L1901435 74M1900809
Products Sold
74K1900074 74K1901335 74L1901435 74M1900809
TELEFLEX MEDICAL INC is recalling Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is indicated to be used in due to Potential sterility issue. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential sterility issue
Recommended Action
Per FDA guidance
Teleflex issued an "Urgent Medical Device Recall" notification on August 7, 2020. It states the following actions to be taken: 1. If you have affected stock in inventory, immediately discontinue use and quarantine any products with the product code and lot number listed, so that the affected products can be returned to Teleflex. 2. To return product, complete the Recall Acknowledgement Form and fax it to 1-855- 419-8507, Attn: Customer Service or email to recalls@teleflex.com. A customer service representative will contact you with a Return Goods Authorization (RGA) Number and will provide instructions for the return of products to Teleflex Medical. 3. If you have no affected stock, please complete the Recall Acknowledgment Form and fax it to 1-855-419-8507, Attn: Customer Service or email to recalls@teleflex.com. If you have any question please contact locals representative or Customer Service at 1-866-396-2111.
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
AZ, AR, CA, CO, FL, GA, IL, IN, IA, LA, MI, MN, MS, NV, NH, NY, NC, OH, OK, OR, PA, SD, TN, TX, VA, WA, WI
Page updated: Jan 10, 2026