Reported Sep 26, 2018 · Terminated

Foley Catheter with temperature sensor 400TM 14FR, Catalogue Number 102201101480TY Product Usage: This is sterile,…

Degania Silicone, Ltd.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Degania Silicone, Ltd. · Degania Bet · Dganya Bet, N/A · N/A

Is this the product you have?

  • Foley Catheter with temperature sensor 400TM 14FR, Catalogue
  • Number 102201101480TY Product UsageThis is sterile, single use, two-way silicone Foley Catheter with a thermistor embedded in the third lumen. It is intended for use in the drainage/ collection of urine from the urinary bladder and simultaneous monitoring of the body core temperature during surgery or post-surgical period
Lot codes and dates
    • S17001226
    • S17002082
    • S17002550
    • S17002784
    • S17002883
    • S17002884
    • S17005004
    • S17003784
    • S17003785
    • S17002982
    • S17002983
    • S17003916
    • S17003917
    • S17004351
    • S17005957
    • S17006689
    • S17007029
    • S17004746
    • S17004877
    • S17005956
    • S17004486
    • S17006334
    • S17005958
    • S17006206
    • S17006333
    • S17006687
    • S17006688
    • S17000191
    • S17000192
    • S17000231
    • S17000320
    • S17000345
    • S17006690
    • S17006926
    • S17007030
    • S17007032
    • S17007334
    • S17007433
    • S17007434
    • S17007588
    • S17008088
    • S17005116
    • S17007031
    • S17003446
    • S17007599
    • S17007780
    • S17000335
    • S17002083
Amount recalled
89122

This recall covers 32 products

The agency filed one notice per product. You are reading one of them; the other 31 are below.

19 more are in the archive.

Where it was sold

Why it was recalled

The catheters are suspected to contain defective sensors; if used, defective catheter will show lower body temperature than the actual body temperature of a patient.

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Oct 25, 2024 · Data as of Sep 19, 4:47 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.