BEUDAMED
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    BD Affirm VPIII Microbial Identification Tests, packaged in kits, 120 test\kit, Catalog # 446257 and 24 test\kit, Catalog # 446252; kits are labeled in part ***Becton, Dickinson and Company, 7 Loveton Circle Sparks, MD 21152 USA, 800-638-8663, www.bd.com/ds*** The Affirm VPIII Microbial Identification Test is a DNA probe test intended for use in the detection and identification of Candida species,

    FDA Recall
    Terminated ·Becton Dickinson & Co. BD Diagnostic Systems·Product code MLA·June 13, 2013

    BD AffirM VPIII Microbial Identification Test

    FDA Recall
    Terminated ·Becton Dickinson & Co. 7 Loveton Cir BD Diagnostic Systems·Product code MLA·August 27, 2015

    Latex-Free Symbiq Pump Set, convertible pin, 106 inch piggyback with backcheck valve, 2 CLAVE ports and OPTION-LOK, 15 drops/mL; a sterile Rx single patient device; Hospira Inc, Lake Forest, IL USA. Made in Costa Rica; product 160080401, list number 16008-01.

    FDA Recall
    Terminated ·Hospira Inc.·Product code FPA·November 24, 2009

    Primary Latex-Free Symbiq Pump Set, piggyback with backcheck valve, 2 prepierced Y-sites, 0.2 micron filter, 104 inch, non-DEHP, 15 drops/mL; a sterile Rx single use device; Hospira Inc, Lake Forest, IL USA. Made in Costa; product 160880428, list number 16088-28.

    FDA Recall
    Terminated ·Hospira Inc.·Product code FPA·November 24, 2009

    Latex-Free Primary Symbiq Pump Set, piggyback with backcheck valve, 2 CLAVE Y-sites, 105 inch, non-DEHP, 15 drops/mL; a sterile Rx single use device; Hospira Inc, Lake Forest, IL USA. Made in Costa Rica; product 160900428, list number 16090-28.

    FDA Recall
    Terminated ·Hospira Inc.·Product code FPA·November 24, 2009

    Latex-Free Symbiq Pump Set, convertible pin, 104 inch piggyback with backcheck valve, 2 CLAVE ports, 0.2 micron filter and OPTION-LOK, non-DEHP, 15 drops/mL; a sterile Rx device; Hospira Inc, Lake Forest, IL USA. Made in Costa Rica; product 160220401, list number 16022-01.

    FDA Recall
    Terminated ·Hospira Inc.·Product code FPA·November 24, 2009

    Primary Symbiq Pump Set, piggyback with backcheck valve, 2 prepierced sites, 105 inch, Latex-Free, non-DEHP, 15 drops/mL; a sterile Rx single use device; Hospira Inc, Lake Forest, IL USA. made in Costa Rica; product 160890428, list number 16089-28.

    FDA Recall
    Terminated ·Hospira Inc.·Product code FPA·November 24, 2009

    Latex-Free Symbiq Pump Set, convertible pin, 106 inch piggyback with backcheck valve, 2 CLAVE ports and OPTION-LOK, non-DEHP, 15 drops/mL; a sterile Rx device; Hospira Inc, Lake Forest, IL USA. Made in Costa Rica; product 160190401, list number 16019-01.

    FDA Recall
    Terminated ·Hospira Inc.·Product code FPA·November 24, 2009

    Primary Symbiq Set, Latex-Free with Polyethylene Lined Tubing, 2 CLAVE Y-sites, backcheck valve, 0.2 micron filter, 20 drops/mL; a sterile Rx single use device; Hospira Inc, Lake Forest, IL USA, Hospira, Finisklin Business Park, Sligo, Ireland, Made in Costa Rica; product 160470701, REF 16047.

    FDA Recall
    Terminated ·Hospira Inc.·Product code FPA·November 24, 2009

    Primary Symbiq Set, 2 CLAVE Y-sites, backcheck valve, 0.2 micron filter, Latex-Free, non-DEHP, 20 drops/mL; a sterile Rx single use device; Hospira Inc, Lake Forest, IL USA, Hospira, Finisklin Business Park, Sligo, Ireland, Made in Costa Rica; product 161010728, REF16101

    FDA Recall
    Terminated ·Hospira Inc.·Product code FPA·November 24, 2009

    Latex-Free Symbiq Pump Set, convertible pin, 106 inch piggyback with backcheck valve, 2 prepierced injection sites, distal microbore tubing and OPTION-LOK, MICRODRIP, non-DEHP, 60 drops/mL; a sterile Rx device, Hospira Inc, Lake Forest, IL USA. Made in Costa Rica; product 160390428, list number 16039-28.

    FDA Recall
    Terminated ·Hospira Inc.·Product code FPA·November 24, 2009

    Latex-Free Symbiq Pump Set, convertible pin, 104.5 inch with Polyethylene-Lined tubing, backcheck valve, 2 CLAVE ports, 0.2 micron filter, and OPTION-LOK, piggyback, 15 drops/mL; a sterile Rx device, Hospira Inc., Lake Forest, IL USA. Made in Costa Rica; product 160130401, list number 16013-01.

    FDA Recall
    Terminated ·Hospira Inc.·Product code FPA·November 24, 2009

    Primary Symbiq Set, Latex-Free, Polyethylene-Lined tubing, piggyback with backcheck valve, 2 CLAVE Y-sites, 0.2 micron filter, 104 inch, non-DEHP, 15 drops/mL; a sterile Rx single use device; Hospira Inc, Lake Forest, IL USA. Made in Costa Rica; product 160930428, list number 16093-28.

    FDA Recall
    Terminated ·Hospira Inc.·Product code FPA·November 24, 2009

    Latex-Free Symbiq Pump Set, convertible pin, 106 inch, piggyback with backcheck valve, 3 CLAVE ports, and OPTION-LOK, non-DEHP, 15 drops/mL; a sterile Rx device; Hospira Inc, Lake Forest, IL USA. Made in Costa Rica; product 160210401, list number 16021-01

    FDA Recall
    Terminated ·Hospira Inc.·Product code FPA·November 24, 2009

    Latex-Free Symbiq Pump Set, convertible pin, 106 inch, piggyback with backcheck valve, 3 prepierced injection sites, and OPTION-LOK, non-DEHP, 15 drops/mL; a sterile Rx device; Hospira Inc, Lake Forest, IL USA. Made in Costa Rica; product 160380428, list number 16038-28.

    FDA Recall
    Terminated ·Hospira Inc.·Product code FPA·November 24, 2009

    Primary Symbiq Pump Set, 2 CLAVE Y-sites, backcheck valve, 0.2 micron filter, Latex-Free, non-DEHP, 20 drops/mL; a sterile Rx single use device; Hospira Inc, Lake Forest, IL USA, Hospira, Finisklin Business Park, Sligo, Ireland, Made in Costa Rica; product 160490728, REF 16049 .

    FDA Recall
    Terminated ·Hospira Inc.·Product code FPA·November 24, 2009

    Primary Symbiq Set, 2 CLAVE Y-sites, backcheck valve, Latex-Free, non-DEHP, 20 drops/mL; a sterile Rx single use device; Hospira Inc, Lake Forest, IL USA, Hospira, Finisklin Business Park, Sligo, Ireland, Made in Costa Rica; product 160980728, REF 16098.

    FDA Recall
    Terminated ·Hospira Inc.·Product code FPA·November 24, 2009

    Primary Symbiq Set, Latex-Free piggyback with backcheck valve, 3 prepierced Y-sites, 106 Inch, non-DEHP, 15 drops/mL; a sterile Rx single use device; Hospira Inc, Lake Forest, IL USA. Made in Costa Rica; product 160960428, list number 16096-28.

    FDA Recall
    Terminated ·Hospira Inc.·Product code FPA·November 24, 2009

    Symbiq Pump Set, detachable, convertible pin piggyback w/backcheck valve, 3 prepierced reseal ports, Option-Lok, Latex-Free, Non-DEHP, 130 in. (330 cm), 15 drops/mL; a sterile Rx single use device; Hospira Inc., Lake Forest, IL 60045 USA, Made in Costa Rica; product 196750428, list number 19675-28

    FDA Recall
    Terminated ·Hospira Inc.·Product code FPA·November 24, 2009

    Latex-Free Symbiq Pump Set, convertible pin, 104 inch piggyback with backcheck valve, 2 prepierced injection sites, 0.2 micron filter and OPTION-LOK, non-DEHP, 15 drops/mL; a sterile Rx single use device; Hospira Inc, Lake Forest, IL USA. Made in Costa Rica; product 160410428, list number 16041-28.

    FDA Recall
    Terminated ·Hospira Inc.·Product code FPA·November 24, 2009