Reported Jul 4, 2018 · Terminated

Amalgatome SD, COAXIAL PNEUMATIC HOSE, SCHRADER, Model X101004

Exsurco Medical

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: Exsurco Medical · 10804 Green Rd · Wakeman, OH · 44889-9676

Is this the product you have?

  • Amalgatome SD, COAXIAL PNEUMATIC HOSE, SCHRADER, Model X101004
Lot codes and dates
  • Serial Numbers

    129 of 129 codes

    • SDH201607220029
    • SDH201607220030
    • SDH201607220031
    • SDH201607220032
    • SDH201607220033
    • SDH201607220034
    • SDH201607220035
    • SDH201607220036
    • SDH201607220037
    • SDH201607220038
    • SDH201607220039
    • SDH201607220040
    • SDH201607220041
    • SDH201607220043
    • SDH201607220044
    • SDH201607220046
    • SDH201607220048
    • SDH201607220049
    • SDH201607220050
    • SDH201607220051
    • SDH201607220052
    • SDH201607220053
    • SDH201607220054
    • SDH201607220055
    • SDH201607220056
    • SDH201607220057
    • SDH201607220058
    • SDH201607220059
    • SDH201607220060
    • SDH201607220061
    • SDH201607220062
    • SDH201607220063
    • SDH201607220064
    • SDH201607220065
    • SDH201607220067
    • SDH201607220068
    • SDH201607220069
    • SDH201607220070
    • SDH201607220071
    • SDH201607220072
    • SDH201607220073
    • SDH201607220075
    • SDH201607220076
    • SDH201607220077
    • SDH201607220078
    • SDH201607220079
    • SDH201607220080
    • SDH201607220081
    • SDH201607220082
    • SDH201607220083
    • SDH201607220084
    • SDH201607220085
    • SDH201607220086
    • SDH201607220087
    • SDH201607220088
    • SDH201607220089
    • SDH201607220090
    • SDH201607220091
    • SDH201607220092
    • SDH201607220093
Amount recalled
70 coaxial hoses

Where it was sold

Why it was recalled

Improper installation of hand piece may result in a weakening of the internal hose connection which can cause loss of pressure to the device or a hose burst.

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

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Jun 15, 2020 · Data as of Sep 19, 4:45 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.