Reported Apr 3, 2019 · Terminated

MultiDiagnost-Eleva, Product codes 708032, 708036 Product Usage: As a multifunctional I universal imaging application…

Philips North America, LLC

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: Philips North America, LLC · 3000 Minuteman Rd · Andover, MA · 01810-1032

Is this the product you have?

    • MultiDiagnost-Eleva
    • Product codes 708032
    • 708036
  • Product UsageAs a multifunctional I universal imaging application system, General RIF, Fluoroscopy, Radiography and Angiography can be performed along with more specialized interventional applications on human patients. This
  • includes the following general areasDigestive
  • systemSwallowing studies, Oesophagus, Stomach, Small intestine, Colon, Defeacography, ERCP, T-tube cholangiogram, Liver biopsies, Transjugular Intrahepatic Portosystemic
  • Shunts (TIPS) Skeletal systemBone studies
  • Urinary systemIVP, Cystograms, Percutaneous, Nephrolithotomy, Nephrostomy
  • tube replacement Reproductive systemHysterosalpingogram, Vena spermatica
  • Cavernography Respiratory systemThorax, Bronchoscopy
  • Pulmonary biopsies Circulatory systemVenography, Arteriography, Thrombolytic Therapy, Em bolizations, Em bolectomy, IVC filter placement, Dilatations, Stent placement
  • VariousArthrograms, Myelograms, Facet joint injections, Discography, Sialography
Lot codes and dates
  • 4 5 7 8 9 10 11 11 12 12 13 13 14 14 14 15 16 16 17 18 18 19 20 21 21 24 24 25 25 26 26 27 28 29 29 29 30 31 31 32 32 33 34 34 35 35 36 36 37 37 38 39 40 40 41 41 42 42 43 43 44 45 46 47 47 48 48 49 49 50 51 52 53 54 55 56 57 59 61 62 67 68 71 72 73 74 75 76 77 81 83 84 84 85 86 87 88 89 90 91 92 93 98

    234 of 234 codes

    • 102
    • 103
    • 104
    • 105
    • 106
    • 107
    • 108
    • 109
    • 110
    • 112
    • 113
    • 114
    • 116
    • 118
    • 119
    • 120
    • 121
    • 122
    • 123
    • 123
    • 124
    • 125
    • 126
    • 127
    • 128
    • 129
    • 130
    • 132
    • 133
    • 135
    • 136
    • 137
    • 138
    • 139
    • 140
    • 142
    • 143
    • 145
    • 151
    • 153
    • 154
    • 157
    • 159
    • 160
    • 161
    • 162
    • 163
    • 164
    • 165
    • 166
    • 169
    • 170
    • 171
    • 172
    • 173
    • 174
    • 178
    • 180
    • 181
    • 182
Amount recalled
1969

This recall covers 6 products

The agency filed one notice per product. You are reading one of them; the other 5 are below.

Where it was sold

  • Nationwide

Why it was recalled

The locking plate may be missing from the system, which may result in unexpected stand/table tilt movement that cannot be stopped by the user.

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 Aug 3, 2020 · Data as of Sep 19, 4:51 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.