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Displaying 1 - 11 of 11 items.
Self-Righting Luer Slip And Lock Tip Caps
Baxter Corporation is issuing an urgent medical device recall for all non-expired lots of Self-Righting Luer Slip And Luer Lock Tip Caps listed due to the potential of the packaging seal not maintaining a sterile barrier for the tip caps.
Recall start…
RecallHealth product recall | 2022-08-02
Omniwire Pressure Guide Wire J-Tip
Potentially non-sterile intravascular device shipped to customers.
Recall start date: May 30, 2022
RecallHealth product recall | 2022-06-13
Evolve Triad Plate Cutter
Stryker has identified a nonconformance relating to the Evolve Triad Plate Cutter provided in the Evolve Triad Instrument Kit (4951kit1). Specifically, the plate cutter is unable to meet sterilization requirements when it is sterilized in a double…
RecallHealth product recall | 2022-06-13
Yelloport Elite Universal Seal
During the manufacturing process, there is a slight risk of the formation of a hole in the sterile packaging which typically forms near the pre-sealed area at the bottom of the sterile packaging of the Yelloport Elite Universal Seals.
Recall start…
RecallHealth product recall | 2022-06-13
Cardinal Health - Presource Kits
BD is conducting a voluntary medical device recall for multiple lots of the BD Posiflush SF (sterile field) saline flush syringe 10ml. This product has been confirmed to exhibit holes in the packaging, which impacts package integrity and potentially…
RecallHealth product recall | 2022-06-13
Tornado, Nestor and Hilal Embolization Microcoils
Cook Medical identified during manufacturing that an unintended small stainless-steel cannula may be contained in the loading cartridge of these devices. This loading cartridge is manufactured by an external supplier.
Recall start date: May 6, 2022
RecallHealth product recall | 2022-05-30
Alliance Earloop Procedure Mask
Mold was found in lot Y591676 of the product. Two species of mold were identified that could pose a potential health risk to users.
Recall start date: May 3, 2022
RecallHealth product recall | 2022-05-30
I-Visc 1%
Our contract manufacturer sent us a FSCA identifying deviations in their sterilisation process and therefore we can not guarantee the sterility of the products.
Recall start date: May 18, 2022
RecallHealth product recall | 2022-05-30
Volista Surgical Lights
Maquet S.A. received customer complaints regarding a paint chipping issue on the component (reference ARD568801164) located on the fork of the Volista Standop SF & DF cupolas.
Recall start date: May 16, 2022
RecallHealth product recall | 2022-05-30
Pico50 Arterial Blood Sampler
Radiometer has been performing integrity testing of the Pico50 arterial blood sampler packaging material. Integrity studies included sterility testing to show that the integrity of the sterile barrier system is intact. In the 24 month real time study, 1…
RecallHealth product recall | 2022-04-25
Acufex Access Advanced Positioning Kits
Smith & Nephew, Inc., has initiated a field action to voluntarily remove three lots of the Acufex Access Advanced Positioning Kits due to the sterilization omission. The affected products were inadvertently shipped to the global distribution center…
RecallHealth product recall | 2021-12-21