BEUDAMED
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    Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044

    FDA Recall
    Open, Classified ·Covidien LLC·Product code BZT·April 23, 2026

    Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050

    FDA Recall
    Open, Classified ·Covidien LLC·Product code BZT·April 23, 2026

    Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF: 90042

    FDA Recall
    Open, Classified ·Covidien LLC·Product code BZT·April 23, 2026

    Cincinnati Sub Zero, Steri-Probe Temperature Probe, Esophageal/Rectal Temperature Probe, Part Number: 39622, Catalog #491B. TA disposable temperature probe used in conjunction with a measuring/monitoring device to continuously measure/monitor a patient's core body temperature.

    FDA Recall
    Terminated ·Cincinnati Sub-Zero Products Inc·Product code BZT·September 26, 2011

    Terumo BCT Lakewood, CO 80215, Catalog No 61000 Spectra Optia Apheresis System, Country of Origin: US. Product Usage: For use in humans. Within the US marketplace, this device is approved for use in Therapeutic Plasma Exchange. Internationally, this device is approved for use in Mono Nucleo Cell engraftment.

    FDA Recall
    Terminated ·CaridianBCT, Inc.·Product code LKN·May 4, 2012

    HARVEST TERUMOBCT, GCP-10 Graft Delivery Pack, REF 51449, Rx Only, STERILE EO Harvest Graph Delivery System is a disposable pack that takes the cell concentrate created while using the BMAC Procedure Packs and allows for hydration of bone graft material for application to the sites doctors deem necessary

    FDA Recall
    Terminated ·Terumo BCT, Inc.·Product code FMF·October 20, 2017

    HARVEST(R) TERUMOBCT, BMAC-30-07 Bone Marrow Procedure Pack, Private Practice / Clinical Use Only, REF 51416, Rx Only, STERILE EO

    FDA Recall
    Terminated ·Terumo BCT, Inc.·Product code JQC·October 20, 2017

    HARVEST(R) TERUMOBCT, BMAC2-120-01Bone Marrow Procedure Pack, REF 51423, Rx Only, STERILE EO

    FDA Recall
    Terminated ·Terumo BCT, Inc.·Product code JQC·October 20, 2017

    Adiprep Adipose Transfer System. Product Codes: 51431; 51432; 51433; 514001-347.

    FDA Recall
    Terminated ·Terumo BCT, Inc.·Product code MUU·November 3, 2016

    Caridian BCT COBE Spectra System Blood Warmer, Catalog number 950000000.

    FDA Recall
    Terminated ·CaridianBCT, Inc.·Product code LKN·October 26, 2011

    Spectra Optia Apheresis System, REF: 61000, Caridian BCT, Lakewood, CO 80215. A blood component separator used for therapeutic plasma exchanges.

    FDA Recall
    Terminated ·Caridian BCT, Incorporated·Product code LKN·September 21, 2011

    Burlington Medical, BAT (Breast, Axilla and Thyroid) Coverage.

    FDA Recall
    Open, Classified ·Burlington Medical, LLC·Product code IWO·February 11, 2026

    DispoSystem for BCT System.Model number OVFR03. Multipurpose System for in vitro coagulation studies.

    FDA Recall
    Terminated ·Dade Behring Inc. Rte 896, Glasgow Business Community·Product code JPA·August 27, 2004

    Spectra Optia apheresis system, a blood component separator. Part No. 61000, Gambro BCT Lakewood, CO USA 80215.

    FDA Recall
    Terminated ·Gambro BCT, Inc.·Product code LKN·September 18, 2007

    Trima Accel Automated Blood Collection System, catalog number 917000000, Caridian BCT, Lakewood, CO 80215 USA. Product Usage: Automated Blood Collection System for use in humans.

    FDA Recall
    Terminated ·CaridianBCT, Inc.·Product code KZE·June 1, 2010

    Cyto-Chex BCT - blood specimen collection device - Immunophenotyping Preservative. IVD. Sterile. 2.0ml only. Packaged 6-tube pack REF 213559 and 100-tube box REF 218980. Streck.

    FDA Recall
    Open, Classified ·Streck·Product code GIM·February 23, 2017

    Singles carbides by Meisinger, US-No: 245, Sterile R, cylinder round end; US-No 245; Reference: HMUN245-009; Shank: FG/314; Head Size 1/10mm: 009,Head Length/mm:

    FDA Recall
    Open, Classified ·Hager & Meisinger Gmbh Ronsdorferstrasse 22 Dusseldorf Germany·Product code EJL·November 7, 2018

    Advisor Vital Signs Monitor model 9200, catalog number 925454325. Item Description 9200 II 3LD/RP/02/IP/TP/BAT MDD. The basic monitoring package includes ECG (3 lead / 5 lead), impedance respiration, non-invasive blood pressure, pulse oximetry, two invasive blood pressures, and tow temperature channels. The device permits patient monitoring with adjustable alarm limits as well as visible and audible alarm signals.

    FDA Recall
    Terminated ·Smiths Medical PM, Inc.·Product code DPS·January 5, 2005

    Blue Belt Technologies, Inc. Monitor Drape REF: PFSD-V0001, Rx only, Sterile EO. Product Usage: The intended use of this device is t protect equipment from contamination during a variety of procedures throughout the clinical setting.

    FDA Recall
    Terminated ·Blue Belt Technologies MN·Product code KKX·July 19, 2013

    MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner cartons per Case (CS). Labeled as follows: a. ET LENGTH DOUBLE SWIVEL, 12 Fr, Item Number/REF: DYNCPDS12; b. ET LENGTH DOUBLE SWIVEL, 14 Fr, Item Number/REF: DYNCPDS14; c. ET LENGTH DOUBLE SWIVEL, 16 Fr, Item Number/REF: DYNCPDS16

    FDA Recall
    Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code BSY·August 3, 2022