Reported Jul 23, 2014 · Terminated

Integra Camino 110-4 Intracranial Pressure (ICP) Monitoring Catheters, Cat. No's. 110-4B, 110-4G, 110-4H, 110-4L

Integra LifeSciences Corp.

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: Integra LifeSciences Corp. · 311 Enterprise Dr · Plainsboro, NJ · 08536-3344

Is this the product you have?

  • Integra Camino 110-4 Intracranial Pressure (ICP) Monitoring Catheters, Cat. No's. 110-4B, 110-4G, 110-4H, 110-4L
Lot codes and dates
  • 289 of 289 codes

    • Catog No. 110-4B
    • Lot No.: 305000222640
    • 305000223280
    • 305000223866
    • 305000223867
    • 305000224353
    • 305000225045
    • 305000225632
    • 305000225633
    • 305000226127
    • 305000226836
    • 305000226844
    • 305000227128
    • 305000228521
    • 305000228522
    • 305000228971
    • 305000229328
    • 305000229329
    • 305000229825
    • 305000229826
    • 305000230302
    • 305000230303
    • 305000230780
    • 305000230781
    • 305000231461
    • 305000231462
    • 305000232098
    • 305000232099
    • 305000232604
    • 305000232605
    • 305000233240
    • 305000233241
    • 305000233242
    • 305000233243
    • 305000233607
    • 305000233608
    • 305000234304
    • 305000235022
    • 305000236104
    • 305000236105
    • 305000236653
    • 305000236655
    • 305000237232
    • 305000238263
    • 305000238818
    • 305000238819
    • 305000242236
    • 305000243881
    • 305000243883
    • 305000243889
    • 305000244481
    • 305000244934
    • 305000245408
    • 305000245835
    • 305000246460
    • 305000247007
    • 305000247717
    • 305000248479
    • 305000249072
    • 305000249743
Amount recalled
28,752 units

Why it was recalled

Integra LifeSciences is recalling the Camino Intracranial Pressure Monitoring Kits because of revised labelling to indicate they are unsafe in an MR environment.

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 Oct 14, 2014 · Data as of Sep 19, 6:04 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.