Reported Apr 26, 2017 · Terminated

Alcon Patient Care Kits Product Usage: A Patient Care Kit is an assemblage of single-use medical devices and…

Alcon Research, 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: Alcon Research, Ltd. · 6201 South Fwy · Fort Worth, TX · 76134-2099

Is this the product you have?

  • Alcon Patient Care Kits Product UsageA Patient Care Kit is an assemblage of single-use medical devices and accessories designed by medical professionals for specific procedures. The Patient Care kits are configured with customer-specific components
Lot codes and dates
  • 124 of 124 codes

    • SPCK50319
    • SPCK50317
    • SPCK50304
    • SPCK50277
    • SPCK50263
    • SPCK50262
    • SPCK50244
    • SPCK50241
    • SPCK50233
    • SPCK50229
    • SPCK50227
    • SPCK50224
    • SPCK50223
    • SPCK50221
    • SPCK50218
    • SPCK50208
    • SPCK50207
    • SPCK50205
    • SPCK50203
    • SPCK50202
    • SPCK50198
    • SPCK50196
    • SPCK50193
    • SPCK50192
    • SPCK50187
    • SPCK50182
    • SPCK50180
    • SPCK50177
    • SPCK50176
    • SPCK50174
    • SPCK50172
    • SPCK50171
    • SPCK50168
    • SPCK50164
    • SPCK50162
    • SPCK50155
    • SPCK50149
    • SPCK50148
    • SPCK50142
    • SPCK50141
    • SPCK50135
    • SPCK50134
    • SPCK50129
    • SPCK50128
    • SPCK50126
    • SPCK50119
    • SPCK50115
    • SPCK50113
    • SPCK50112
    • SPCK50107
    • SPCK50103
    • SPCK50102
    • SPCK50100
    • SPCK50099
    • SPCK50097
    • SPCK50096
    • SPCK50094
    • SPCK50091
    • SPCK50083
    • SPCK50075
Amount recalled
561,702

Where it was sold

  • Nationwide

Why it was recalled

Alcon is initiating a Voluntary Medical Device Removal because the product supplier has stated that there is potential for sterile packaging to be compromised.

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 Dec 5, 2017 · Data as of Sep 19, 6:51 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.