Reported Oct 10, 2018 · Terminated

CAPNOSTREAM 20P (INTL) N, Part Number CS08652-01

Oridion Medical 1987 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: Oridion Medical 1987 Ltd. · Har Hotzvim Industrial Park Box 45025 · Jerusalem · N/A

Is this the product you have?

    • CAPNOSTREAM 20P (INTL) N
    • Part Number CS08652-01
Lot codes and dates
  • 113 of 113 codes

    • B642138114
    • B642138116
    • B642138122
    • B643138126
    • B643138128
    • B643138132
    • B643138134
    • B643138139
    • B643138144
    • B643138146
    • B643138150
    • B643138153
    • B643138156
    • B643138160
    • B643138166
    • B643138167
    • B643138168
    • B643138169
    • B643138170
    • B643138171
    • B643138172
    • B643138175
    • B643138177
    • B643138179
    • B643138181
    • B643138182
    • B643138190
    • B643138192
    • B643138215
    • B643138216
    • B643138217
    • B643138218
    • B643138219
    • B643138222
    • B643138224
    • B643138225
    • B643138228
    • B643138230
    • B643138232
    • B643138233
    • B643138240
    • B643138241
    • B643138243
    • B643138245
    • B643138253
    • B644138256
    • B644138259
    • B644138286
    • B644138287
    • B644138291
    • B610148829
    • B610148834
    • B610148838
    • B610148845
    • B611148924
    • B611148945
    • B611148946
    • B611148951
    • B612149038
    • B612149039
Amount recalled
113

This recall covers 37 products

The agency filed one notice per product. You are reading one of them; the other 36 are below.

24 more are in the archive.

Where it was sold

  • Nationwide
  • PR

Why it was recalled

The date/time, nurse call and alarm settings of the bedside patient monitors may reset to the factory default settings when the monitor is powered off.

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

Want the full recall guide?

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 Sep 20, 2022 · Data as of Sep 19, 6:55 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.