Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Pilling Modular Verres Body/Obturator Recalled by Teleflex Medical Due to Packaging error in which customers who ordered product...
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 directly.
Affected Products
Pilling Modular Verres Body/Obturator, Product Code 140880
Quantity: 8
Why Was This Recalled?
Packaging error in which customers who ordered product code 140880 (Verres cannula for use with a separately available needle tip) were incorrectly provided with product code 140878 (Verres cannula with integral needle tip).
Where Was This Sold?
This product was distributed to 1 state: UT
About Teleflex Medical
Teleflex Medical has 204 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report