112 results
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19ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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BLUE BURN SHEET, STERILE, 60" x 96"; Item 7305, GAM item 30-01 Product Usage - May provide a sterile, barrier environment to protect patient from infection.
FDA Recall
Terminated
·Dukal Corp.·Product code FPY·June 1, 2017
API Listeria (REF 10300) API Listeria is a standardized system for the identification of Listeria which uses miniaturized tests, as well as a database. The ZYM B reagent is including in API Listeria kit and it is used as an additional reagent for revealing the result of DIM miniaturized biochemical test included in the API Listeria strips. ZYM B reagent is added in the DIM test before reading miniaturized biochemical test including in the API Listeria strips.
FDA Recall
Terminated
·Biomerieux France Chemin De L'Or Chemin De L'Orme Marcy L'Etoile France·November 8, 2013
API NH (REF 10400) API NH is a standardized system for the identification of Neisseria, Haemophilus (and related genera) and Moraxella catharrhalis (Branhamella catarrhalis), which uses miniaturized tests, as well as a specially adapted database. API NH also enables the biotyping of Haemophilus influenza and Haemophilus parainfluenxzae, as well as the detection of a penicllinase.
FDA Recall
Terminated
·Biomerieux France Chemin De L'Or Chemin De L'Orme Marcy L'Etoile France·November 8, 2013
ZYM B Reagent (REF 70493) ZYM B reagent is an additional test used to reveal the results of some miniaturized biochemical test included in the API strips. The API product line is a standardized system combining several biochemical tests, which enables group or species identifications of microorganisms.
FDA Recall
Terminated
·Biomerieux France Chemin De L'Or Chemin De L'Orme Marcy L'Etoile France·November 8, 2013
API Listeria (REF 10300). ZYM B reagent is used and included inside of API NH (REF 10400) and API Listeria (10300). All of the APIs are standardized systems combining several biochemical tests that enable group or species identification of most microorganisms.
FDA Recall
Terminated
·BioMerieux SA Chemin De L'Orme Marcy L'Etoile France·Product code LIB·March 6, 2014
API NIH (REF 10400). ZYM B reagent is used and included inside of API NH (REF 10400) and API Listeria (10300). All of the API's are standardized systems combining several biochemical tests that enable group or species identification of most microorganisms.
FDA Recall
Terminated
·BioMerieux SA Chemin De L'Orme Marcy L'Etoile France·Product code LIB·March 6, 2014
API ZYM Bx2 (Ref 70493) Product Usage: ZYM B reagent is an additional test used for revealing the results of some miniaturized biochemical test including in the involved API strips.
FDA Recall
Terminated
·BioMerieux SA Chemin De L'Orme Marcy L'Etoile France·Product code LIB·January 8, 2016
FB Reagent (REF 70562). FB reagent is an additional test used for revealing the results of some miniaturized biochemical test included in the API and Rapid ID 32 strips. The API and ID 32 strips product lines are a standardized system combining several biochemical tests, which enables group or species identifications of microorganisms.
FDA Recall
Terminated
·BioMerieux SA Chemin De L'Orme Marcy L'Etoile France·Product code LIB·March 6, 2014
ZYM B Reagent (REF 70493). The ZYM B reagent is an additional test used to reveal the results of some miniaturized biochemical test included in the API strips. The API product line is a standardized system combining several biochemical tests, which enables group or species identifications of microorganisms.
FDA Recall
Terminated
·BioMerieux SA Chemin De L'Orme Marcy L'Etoile France·Product code LIB·March 6, 2014
Medefil Heparin I.V. Flush Syringe 1 unit/mL; a polypropylene luer locking syringe containing Heparin Lock Flush Solution, USP, a sterile non-pyrogenic, isotonic injection; each mL in a Heparin I.V. Flush Syringe contains 1 unit of heparin sodium derived from porcine intestinal mucosa and 9 mg of sodium chloride in water for injection; Medefil, Inc., Glendale Heights, IL 60139 The 5 mL fill in 6 mL syringes were packed 60 syringes per dispenser box, 16 boxes per shipping carton, NDC #64253-444-25, catalog #MIH-4425
FDA Recall
Terminated
·Medefil Incorporated·Product code NZW·March 20, 2008
Medefil Heparin I.V. Flush Syringe 10 units/mL; a polypropylene luer locking syringe containing Heparin Lock Flush Solution, USP, a sterile non-pyrogenic, isotonic injection; each mL in a Heparin I.V. Flush Syringe contains 10 units of heparin sodium derived from porcine intestinal mucosa and 9 mg of sodium chloride in water for injection; Medefil, Inc., Glendale Heights, IL 60139 The pre-filled syringes were packed 60 syringes per dispenser box, 16 boxes per shipping carton in the following syringe configurations: a) NDC #64253-222-35, catalog #MIH-2235: 5 mL fill in 12 mL syringe b) NDC #64253-222-33, catalog #MIH-2233: 3 mL fill in 12 mL syringe
FDA Recall
Terminated
·Medefil Incorporated·Product code NZW·March 20, 2008
API JAMES 2AMP, CATALOG 70542
FDA Recall
Open, Classified
·Biomerieux Inc·Product code JTO·November 9, 2022
API 50 CH, Model 50300
FDA Recall
Terminated
·bioMerieux, Inc.·Product code JSC·September 30, 2021
API NIT1 NIT2 REAGENTS, CATALOG 70442
FDA Recall
Open, Classified
·Biomerieux Inc·Product code JTO·November 9, 2022
API VP1 VP2 REAGENTS, CATALOG 70422
FDA Recall
Open, Classified
·Biomerieux Inc·Product code JTO·November 9, 2022
Medifil Heparin I.V. Flush Syringe 100 units/mL; a polypropylene luer locking syringe containing Heparin Lock Flush Solution, USP, a sterile non-pyrogenic, isotonic injection; each mL in a Heparin I.V. Flush Syringe contains 100 units of heparin sodium derived from porcine intestinal mucosa and 9 mg of sodium chloride in water for injection; Medefil, Inc., Glendale Heights, IL 60139 The pre-filled syringes were packed 60 syringes per dispenser box, 16 boxes per shipping carton in the following syringe configurations: a) NDC #64253-333-35, catalog #MIH-3335: 5 mL fill in 12 mL syringe b) NDC #64253-333-33, catalog #MIH-3333: 3 mL fill in 12 mL syringe c) NDC #64253-333-23, catalog #MIH-3323: 3 mL fill in 6 mL syringe
FDA Recall
Terminated
·Medefil Incorporated·Product code NZW·March 20, 2008
API 20 E 25 STRIPS, CATALOG 20100
FDA Recall
Open, Classified
·Biomerieux Inc·Product code JSS·November 9, 2022
API STAPH 25 STRIPS+25 MEDIA, CATALOG 20500
FDA Recall
Open, Classified
·Biomerieux Inc·Product code JWX·November 9, 2022
API LISTERIA 10 STRIPS+10 MEDIA, CATALOG 10300
FDA Recall
Open, Classified
·Biomerieux Inc·Product code JTO·November 9, 2022
API 20 C AUX 25 STRIPS+25 MEDIA, CATALOG 20210
FDA Recall
Open, Classified
·Biomerieux Inc·Product code JXB·November 9, 2022