13 results
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11ms
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Sources: EU EUDAMED, US FDA
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Status: Terminated
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Howmedica Osteonics Corp., Scorpio NRG Femoral Size 7 Right; Knee prosthesis (Stryker France). Product Code: 814407R. Mahwah, NJ
FDA Recall
Terminated
·Stryker Howmedica Osteonics Corp.·Product code JWH·August 20, 2007
MEDLINE O.R. Necessities(R) STERILE R, Needle Counter/Compte-aiguiles/Caja de agujas, Gold Standard/Standard Or/Oro y Estander, 40 Ct. Foam Block / Magnet with Blade Remover, Coussinet en mousse pour 40 aiguilles /Magnetise avec quitte-lame Or, 40 Ct Bloque de espuma / Iman Con extractor de hoja - Oro, REF NC40FBRGS Product Usage: A needle counter is intended to be used safely and easily accounting for used, disposable surgical sharps during a surgical procedure. The product does not come in contact with the surgical site or the patient.
FDA Enforcement
Class II
·Terminated·Medline Industries Inc·June 6, 2018
i-STAT PT/INR Cartridge Abbott Point of Care, Princeton, NJ
FDA Recall
Terminated
·Abbott Point of Care Inc.·Product code GJS·May 5, 2010
BD Vacutainer Urine Complete Kit with UA Preservative Tube and C&S Preservative Tube for Midstream Specimens PLUS Plastic, Sterile Cup and Tube Interiors. Store at 4-25 degrees C. For In Vitro Diagnostic Use. Becton Dickinson and Company, Franklin Lakes, NJ.
FDA Recall
Terminated
·Becton Dickinson & Company·Product code JSM·October 12, 2009
BD Vacutainer Urine Complete Kit with UA Tube and S&C Preservative Tube for Midstream specimens; Plus Plastic - Sterile Cup and Tube interiors. Store at 4-25 degrees C. Kit contains Sterile Screw CAP Collection Cup with integrated Transfer Device and 8.0 mL, 16/x100 mm PLUS Plastic Conical Tube for Urinalysis and 4.0 mL 13x75mm Plus Plastic C&C Preservative tube and Castile Soap Towelettes; Becton Dickinson and Company, Franklin Lakes, NJ
FDA Recall
Terminated
·Becton Dickinson & Company·Product code JSM·October 12, 2009
KODAK T-MAT G/RA Film, Catalog/REF # 151 0023, 24x30 cm, 5-100 Sheet Boxes FOLHAS/Hojas, Made in U.S.A. by Carestream Health, Inc. 150 Verona Street, Rochester, NY 14608 --- Device Listing # E420904 Intended use: Imaging film
FDA Recall
Terminated
·Carestream Health, Inc.·Product code IWZ·March 12, 2010
KODAK T-MAT L/RA Film, Catalog/REF # 181 4631, 35x43 cm 5-100 Sheet Boxes Folhas/Hojas, Made in U.S.A. by Carestream Health, Inc. 150 Verona Street, Rochester, NY 14608 --- Device Listing # E420904 Intended use: Imaging film
FDA Recall
Terminated
·Carestream Health, Inc.·Product code IWZ·March 12, 2010
MEDLINE O.R. Necessities(R) STERILE R, Needle Counter/Compte-aiguiles/Caja de agujas, Gold Standard/Standard Or/Oro y Estander, 40 Ct. Foam Block / Magnet with Blade Remover, Coussinet en mousse pour 40 aiguilles /Magnetise avec quitte-lame Or, 40 Ct Bloque de espuma / Iman Con extractor de hoja - Oro, REF NC40FBRGS Product Usage: A needle counter is intended to be used safely and easily accounting for used, disposable surgical sharps during a surgical procedure. The product does not come in contact with the surgical site or the patient.
FDA Recall
Terminated
·Medline Industries Inc·Product code GAB·April 24, 2018
BC Thrombin Reagent . Thrombin Time Test
FDA Recall
Terminated
·Dade Behring Inc. Rte 896, Glasgow Business Community·Product code GJA·July 21, 2004
BC Thrombin Reagent Kit Lot Number 46751; UDI - 008427680131024675120180908 and BC Thrombin Reagent Kit Lot Number 47184; UDI -008427680131024718420190221; BC Thrombin Reagent; Test, Thrombin Time Product Usage: For in vitro diagnostic use. Reagent for the quantitative determination of the thrombin time in citrated human plasma.
FDA Recall
Terminated
·Siemens Healthcare Diagnostics·Product code GJA·October 17, 2017
MDA Fibriquik, bioMeriux, Inc., Box 15969, Durham, North Carolina 27704-0969
FDA Recall
Terminated
·bioMerieux·Product code GJA·August 20, 2004
Fibriquik, bioMeriux, Inc., Box 15969, Durham, North Carolina 27704-0969
FDA Recall
Terminated
·bioMerieux·Product code GJA·August 20, 2004
Evolve Cell Culture Bags, part numbers: EV1000N and EV3000N The Evolve bag is made of Ethyl Vinyl Olefin (EVO) and contains no BPA or latex. The bag can be supplied with tubing sets that can include, but are not limited to, the following components: EVA/PVC coextruded tubing, PVC tubing, Yconnectors, needle-free valves, female luers, male luers and/or caps
FDA Recall
Terminated
·OriGen Biomedical, Inc.·Product code KJA·January 28, 2021