Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Teflon Tube Recalled by Stryker Howmedica Osteonics Corp. Due to Stryker became aware during laboratory testing that there...
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 Stryker Howmedica Osteonics Corp. directly.
Affected Products
Teflon Tube, sterile T2 Humerus System Stryker Trauma GmbH Prof Kuntscher Str 1-5 24232 Sconkidrchen, Germany distributed in the USA by: Stryker Howmedica Osteonics Corp.: Mahwah, NJ 07430 USA 510 K042396 Used in several T2 systems intended to support the exchange of the Ball Tip Guide Wires for Smooth Tip Guide Wires: T2 Tibial Nailing Systems, T2 Femoral Nailing Systems, T2 Ankle Nailing Systems, and T2 Humerus Nailing Systems
Quantity: 34 units
Why Was This Recalled?
Stryker became aware during laboratory testing that there is a potential that the seal integrity of the outer pouch (sterile barrier) may be compromised for certain lots of the product Teflon Tube, sterile.
Where Was This Sold?
This product was distributed to 9 states: GA, IL, KY, MI, MO, NJ, TN, UT, VA
About Stryker Howmedica Osteonics Corp.
Stryker Howmedica Osteonics Corp. has 87 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report