BEUDAMED
    24 results · 21ms · Sources: EU EUDAMED, US FDA

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    Stryker Medical Stair-PRO Stair Chair with wheels and a track system, patient transport device, Model 6252.

    FDA Recall
    Terminated ·Stryker Medical Div. of Stryker Corporation·Product code FPP·September 2, 2009

    Paramed Polypropylene evacuation sled for non-ambulatory patients. Hand-carried stretcher. Product 11-778-01.

    FDA Recall
    Terminated ·Paramed Systems·Product code FPP·October 29, 2008

    Stryker Medical Stair-PRO Stair-Chair with wheels, patient transport device, Model 6251.

    FDA Recall
    Terminated ·Stryker Medical Div. of Stryker Corporation·Product code FPP·November 18, 2008

    Foot Rest Kit (pN 6252700-003) for Models 6251 and 6252 Stryker (EMS Stair -PRO), OE 2065939, 1739631, 2066066, 6066803 and 20666941 with optional , Stryker Medical, Portage, MI 49002. Intended to provide the patient greater comfort and a sense of security.

    FDA Recall
    Terminated ·Stryker Medical Division of Stryker Corporation·Product code FPP·October 31, 2011

    TransMotion Medical, TMM3 Series Video-Fluoroscopy Swallow Study Stretcher-Chair. Intended use is to provide the caregiver a single platform for receiving, transporting within a facility, performing procedures, recovery and discharge of patients in a monitored outpatient environment.

    FDA Recall
    Terminated ·Winco Mfg., LLC·Product code FPP·June 29, 2016

    Stryker Medical Stair-PRO Evacuation Chair civilian use stair chair, patient transport device, Model 6253.

    FDA Recall
    Terminated ·Stryker Medical Div. of Stryker Corporation·Product code FPP·November 18, 2008

    Stryker Evacuation Chair Model 6254 It Is intended to aid in the transportation of passengers up and/or down a flight of stairs in an evacuation situation.

    FDA Recall
    Terminated ·Stryker Medical Division of Stryker Corporation·Product code FPP·June 28, 2011

    TransMotion Medical, TMM4 Series Multi-Purpose Treatment Chair. Intended use is to provide the caregiver a single platform for receiving, transporting within a facility, performing procedures, recovery and discharge of patients in a monitored outpatient environment.

    FDA Recall
    Terminated ·Winco Mfg., LLC·Product code FPP·June 29, 2016

    TransMotion Medical, TMM5 Series Mobile Surgical Stretcher -Chair. Intended use is to provide the caregiver a single platform for receiving, transporting within a facility, performing procedures, recovery and discharge of patients in a monitored outpatient environment.

    FDA Recall
    Terminated ·Winco Mfg., LLC·Product code FPP·June 29, 2016

    Stryker EMS Stair - Pro Evacuation Chair Model 6252 It Is intended to aid in the transportation of passengers up and/or down a flight of stairs in an evacuation situation.

    FDA Recall
    Terminated ·Stryker Medical Division of Stryker Corporation·Product code FPP·June 28, 2011

    Stryker Medical Stair-PRO Stair-Chair with wheels and a track system, patient transport device, Model 6252.

    FDA Recall
    Terminated ·Stryker Medical Div. of Stryker Corporation·Product code FPP·November 18, 2008

    Stryker Medical Stair-PRO Stair Chair with wheels, patient transport device, Model 6251.

    FDA Recall
    Terminated ·Stryker Medical Div. of Stryker Corporation·Product code FPP·September 2, 2009

    HEPARIN LOCK FLUSH SOLUTION, USP, 100 USP Units/mL, 1 mL Multiple Dose Vial, plastic vial, vial size 3 mL, NDC 63323-545-01, Product Code 504501; and HEPARIN LOCK FLUSH SOLUTION, USP, 100 USP Units/mL, 5 mL Multiple Dose Vial, 500 USP Units/5 mL, plastic vial, vial size 6 mL, NDC 63323-545-05, Product Code 504505; Rx only To maintain patency of an indwelling venipuncture device designed for intermittent injection or infusion therapy or blood sampling.

    FDA Recall
    Terminated ·App Pharmaceuticals Llc·Product code NZW·May 20, 2010

    HEPARIN LOCK FLUSH SOLUTION, USP, 10 USP Units/mL, 1 mL Multiple Dose Vial, plastic vial, vial size 3 mL, NDC 63323-544-01, Product Code 504401, Rx only To maintain patency of an indwelling venipuncture device designed for intermittent injection or infusion therapy or blood sampling.

    FDA Recall
    Terminated ·App Pharmaceuticals Llc·Product code NZW·May 20, 2010

    HEPARIN LOCK FLUSH SOLUTION, USP, 100 USP Units/mL, 1 mL Multiple Dose Vial, plastic vial, vial size 3 mL, NDC 63323-545-01, Product Code 504501; and HEPARIN LOCK FLUSH SOLUTION, USP, 100 USP Units/mL, 5 mL Multiple Dose Vial, 500 USP Units/5 mL, plastic vial, vial size 6 mL, NDC 63323-545-05, Product Code 504505; Rx only To maintain patency of an indwelling venipuncture device designed for intermittent injection or infusion therapy or blood sampling.

    FDA Enforcement
    Class II ·Terminated·App Pharmaceuticals Llc·June 27, 2012

    HEPARIN LOCK FLUSH SOLUTION, USP, 10 USP Units/mL, 1 mL Multiple Dose Vial, plastic vial, vial size 3 mL, NDC 63323-544-01, Product Code 504401, Rx only To maintain patency of an indwelling venipuncture device designed for intermittent injection or infusion therapy or blood sampling.

    FDA Enforcement
    Class II ·Terminated·App Pharmaceuticals Llc·June 27, 2012

    Rectal Catheters; Product Code Equivalent Code 580114 580114 Product Usage: Rectal Balloon Catheter is inserted into the rectum to measure the abdominal pressure as bladder filled.

    FDA Recall
    Terminated ·Teleflex Medical Europe Ltd Ida Business Park Athlone Ireland·Product code FAP·March 15, 2018

    Replacement balloons for use with Sandhill Anorectal Manometry Probes. There is no labeling other than the part number for these products.

    FDA Recall
    Terminated ·Sandhill Scientific, Inc·Product code FAP·December 13, 2005

    SNS Disposable Urethral Catheter Electrode, 10 Fr, Gold Recording/Stimulating Contact printed on polyurethane film adhesive with attached 2 meter lead-wire with touch-proof connector, Reference Number UE006

    FDA Recall
    Terminated ·Spes Medica Via Buccari·Product code FAP·April 8, 2021

    SNS Disposable Urethral Catheter Electrode, 14 Fr, Gold Recording/Stimulating Contact printed on polyurethane film adhesive with attached 2 meter lead-wire with touch-proof connector, Reference Number UE002

    FDA Recall
    Terminated ·Spes Medica Via Buccari·Product code FAP·April 8, 2021