Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Rectal Catheters Recalled by Teleflex Medical Europe Ltd Due to These products contain latex, but the following statement...
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 Europe Ltd directly.
Affected Products
Rectal Catheters; Product Code Equivalent Code 580114 580114 Product Usage: Rectal Balloon Catheter is inserted into the rectum to measure the abdominal pressure as bladder filled.
Quantity: 6340 units
Why Was This Recalled?
These products contain latex, but the following statement is not included on any level of product packaging: Caution: This Product Contains Natural Rubber Latex Which May Cause Allergic Reactions.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Teleflex Medical Europe Ltd
Teleflex Medical Europe Ltd has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report