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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 17 Results
Related Medical Device Recalls
 
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Product Description
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FDA Recall
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Z-1359-2023 - Titan Touch Pump, Catalog Numbers 5177502400; inflatable penile Prosthesis 2 04/12/2023 Coloplast Manufacturing US, LLC
Z-1375-2023 - Titan 0-Deg Scrotal 22 Cm, Catalog Number ES89222400; inflatable penile Prosthesis 2 04/12/2023 Coloplast Manufacturing US, LLC
Z-1361-2023 - Titan Touch NB Infr Zero 16cm, Catalog Number EN28162400; inflatable penile Prosthesis 2 04/12/2023 Coloplast Manufacturing US, LLC
Z-1362-2023 - Titan Touch NB Infr Zero 18cm, Catalog Number EN28182400; inflatable penile Prosthesis 2 04/12/2023 Coloplast Manufacturing US, LLC
Z-1363-2023 - Titan Touch NB Scrot Zero 16cm, Catalog Number EN29162400; inflatable penile Prosthesis 2 04/12/2023 Coloplast Manufacturing US, LLC
Z-1364-2023 - Titan Touch NB Scrot Zero 18cm, Catalog Number EN29182400; inflatable penile Prosthesis 2 04/12/2023 Coloplast Manufacturing US, LLC
Z-1365-2023 - Titan NB Infra Zero Ang 16cm, Catalog Number EN88162400; inflatable penile Prosthesis 2 04/12/2023 Coloplast Manufacturing US, LLC
Z-1366-2023 - Titan NB Scrotal Zero Ang 18cm, Catalog Number EN88182400; inflatable penile Prosthesis 2 04/12/2023 Coloplast Manufacturing US, LLC
Z-1367-2023 - Titan Touch Infr Zero Ang 18cm, Catalog Number ES28182400; inflatable penile Prosthesis 2 04/12/2023 Coloplast Manufacturing US, LLC
Z-1368-2023 - Titan Touch Infr Zero Ang 22cm, Catalog Number ES28222400; inflatable penile Prosthesis 2 04/12/2023 Coloplast Manufacturing US, LLC
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