Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is Recalled by TELEFLEX MEDICAL INC Due to Potential sterility issue
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact TELEFLEX MEDICAL INC directly.
Affected Products
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.
Quantity: 700 eaches
Why Was This Recalled?
Potential sterility issue
Where Was This Sold?
This product was distributed to 27 states: 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
About TELEFLEX MEDICAL INC
TELEFLEX MEDICAL INC has 32 total recalls tracked by RecallDetector.
Related Recalls
EndoVive Safety PEG Kit Recalled by Boston Scientific Corporation Due to Recall of kits which utilized ChloraPrep Triple Swabsticks...
Boston Scientific Corporation · February 10, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Artelon FlexBand Dynamic Matrix Ref: 31057 Recalled by International Life Sciences Due to Augmentation devices failed bacterial endotoxin testing.
International Life Sciences · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Data sourced from the FDA (Device). Last updated March 26, 2026. View original report