Medical Device May 29, 2024
Unreleased software was installed on customer systems resulting in the visual feedback on the screen to show the points to be off from the physical reference point of the pointer or suction.
Class II FDA: Ongoing Stryker Leibinger GmbH & Co. KG
Medical Device May 15, 2024
Mislabeled: Product labeled 56-90614 (90x90 Gold Mesh), was actually 56-90314 (90x90 Blue Mesh), may cause a delay in procedure
Class II FDA: Ongoing Stryker Leibinger GmbH & Co. KG
Medical Device Mar 9, 2022
Inside the packaging of one reported item a non-conforming product was found. Contrary to the design, the barrier layer was manufactured on the inferior side of the implant versus the…
Class II FDA: Terminated Stryker Leibinger GmbH & Co. KG
Medical Device Apr 28, 2021
Inability for the user to inject the paste from the syringe into the target location.
Class II FDA: Terminated Stryker Leibinger GmbH & Co. KG
Medical Device Sep 5, 2018
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
Class II FDA: Terminated Stryker Leibinger GmbH & Co. KG
Medical Device Sep 5, 2018
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
Class II FDA: Terminated Stryker Leibinger GmbH & Co. KG
Medical Device Sep 5, 2018
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
Class II FDA: Terminated Stryker Leibinger GmbH & Co. KG
Medical Device Sep 5, 2018
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
Class II FDA: Terminated Stryker Leibinger GmbH & Co. KG
Medical Device Sep 5, 2018
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
Class II FDA: Terminated Stryker Leibinger GmbH & Co. KG
Medical Device Sep 5, 2018
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
Class II FDA: Terminated Stryker Leibinger GmbH & Co. KG
Medical Device Sep 5, 2018
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
Class II FDA: Terminated Stryker Leibinger GmbH & Co. KG
Medical Device Sep 5, 2018
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
Class II FDA: Terminated Stryker Leibinger GmbH & Co. KG
Medical Device Sep 5, 2018
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
Class II FDA: Terminated Stryker Leibinger GmbH & Co. KG
Medical Device Sep 5, 2018
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
Class II FDA: Terminated Stryker Leibinger GmbH & Co. KG
Medical Device Sep 5, 2018
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
Class II FDA: Terminated Stryker Leibinger GmbH & Co. KG
Medical Device Sep 5, 2018
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
Class II FDA: Terminated Stryker Leibinger GmbH & Co. KG
Medical Device Sep 5, 2018
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
Class II FDA: Terminated Stryker Leibinger GmbH & Co. KG
Medical Device Sep 5, 2018
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
Class II FDA: Terminated Stryker Leibinger GmbH & Co. KG
Medical Device Sep 5, 2018
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
Class II FDA: Terminated Stryker Leibinger GmbH & Co. KG
Medical Device Sep 5, 2018
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
Class II FDA: Terminated Stryker Leibinger GmbH & Co. KG
Medical Device Sep 5, 2018
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
Class II FDA: Terminated Stryker Leibinger GmbH & Co. KG
Medical Device Sep 5, 2018
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
Class II FDA: Terminated Stryker Leibinger GmbH & Co. KG
Medical Device Feb 15, 2017
An incorrect sterility status on the label, non-sterile products labeled as sterile
Class II FDA: Terminated Stryker Leibinger GmbH & Co. KG
Medical Device Feb 15, 2017
An incorrect sterility status on the label, non-sterile products labeled as sterile
Class II FDA: Terminated Stryker Leibinger GmbH & Co. KG
Understanding this recall history This page summarizes recall records in which the official source identifies Stryker Leibinger GmbH & Co. KG as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.