International safety notice

Lot recall of Prostaflow Prostatectomy Catheters PVC Latex, Coloplast

Germany / BfArM · DEU · Oct 30, 2013

Key facts

Title Lot recall of Prostaflow Prostatectomy Catheters PVC Latex, Coloplast
Regulator Germany / BfArM
Country DEU
Brand Lot recall of Prostaflow Prostatectomy Catheters PVC Latex, Coloplast
Manufacturer Lot recall of Prostaflow Prostatectomy Catheters PVC Latex, Coloplast
Models 21035, 13485, 3-LUMIG, 22003, AB7220, 22045, 65501, 4989011502, 669807-0, 3-LUMIGE, 02.07.2013, 669807-77 and 5 more
Date Oct 30, 2013
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 10–99 Matching device models in FDA data
  • 10–99 Matching catalog numbers in FDA data

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

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