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Displaying 1 - 5 of 5 items.
Staysafe Disinfection Cap
At the end of August 2022, Fresenius complaint handling unit (Germany) registered a complaint from New Zealand that an infant (no day fill) developed iodine induced hypothyroidism following use of stay safe disinfection cap. Further investigations…
RecallHealth product recall | 2023-10-13
Filter/HME Twinstar Plus
Manufacturer's market surveillance activities revealed cases of increased inspiratory resistance resulting in insufficient ventilation, which may be related to formation of condensate in the filter housing.
Device is intended exclusively for…
RecallHealth product recall | 2023-08-04
Minicap Disconnect Cap With Povidone-Iodine
Baxter Corportation is issuing a recall for certain lots of the Minicap. These devices are packaged in foil pouches, which may have been incorrectly sealed, i.e., the pouches may have open or weak seals.
Baxter is expanding the urgent medical…
RecallHealth product recall | 2023-05-10
Evolut Pro+ Transcatheter Aortic Valve
Infolding is a known phenomenon and occurs when the valve frame folds inward along a vertical line away from the valve inflow and appears as a seam in the frame or as overlapping frame cells on radiographic imaging. Infolding is different and distinct…
RecallHealth product recall | 2022-12-13
Cortrak*2 Enteral Access System (Eas)
Avanos medical is conducting a voluntary field correction for the Cortrak* 2 Enteral Access System (Eas) because modifications to the labeling of the device have been initiated. Reports of injuries and patient deaths related to misplacement of…
RecallHealth product recall | 2022-04-19