FDA recall, , Moderate risk
Integra LifeSciences Codman Microsensor and CereLink ICP Sensor Basic Kits
The Codman Microsensor Basic Kit may have corrosion stains on its included needle.
Summary by Recall Canary from the FDA notice
What happened
Integra LifeSciences Corp. (NeuroSciences) of Princeton, New Jersey began a recall on December 12, 2025, for the Codman Microsensor Basic Kit and the Codman CereLink ICP Sensor Basic Kit due to potential corrosion stains on the surface of the 14-gauge Tuohy Needle included in the kits. The FDA added the recall to its Enforcement Report on January 8, 2026.
The affected products include the Codman Microsensor Basic Kit and the Codman CereLink ICP Sensor Basic Kit, with distribution in the United States and worldwide.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is your kit affected?
2 products
Match the UDI-DI and lot code listed under your product.
A UDI-DI is the device identifier printed with the barcode on the device label.
Codman CereLink ICP Sensor Basic Kit. Catalog Number: 826850. The Codman CereLink ICP Sensor Basic Kit consists of the CereLink ICP Sensor (ICP Sensor) and a 14-gauge Tuohy needle with stylet. The ICP Sensor
- UDI-DI
- 10381780520672
- Lot code
- 7261958
- 7266691
- 7266692
- 7288060
- 7293837
- 7293836
- 7306040
- 7306041
- 7306042
- 7306043
- 7306044
- 7306045
- 7306046
- 7306047
- 7306050
- 7306051
- 7306052
- 7307670
- 7307671
- 7307672
- 7325482
- 7307675
- 7325481
- 7325483
- 7325484
- 7307673
- 7307674
- 7325485
- 7325486
- 7336611
- 7336612
- 7336614
- 7336623
- 7336613
- 7336615
- 7336616
- 7336618
- 7336619
- 7336620
- 7336621
- 7336622
- 7306048
- 7306049
- 7336626
- 7336627
- 7336629
- 7347166
- 7336628
- 7346295
- 7346297
- 7346299
- 7346301
- 7365434
- 7365435
- 7392019
- 7396607
- 7396608
- 7396609
- 7396610
- 7392034
- 7392067
- 7405790
- 7405791
- 7405792
- 7405793
- 7406633
- 7406634
- 7406636
- 7406637
- 7406639
- 7406640
- 7406641
- 7406642
- 7406635
- 7406638
- 7408813
- 7408815
- 7408818
- 7408814
- 7408816
- 7468726
- 7468727
- 7411801
- 7411802
- 7414641
- 7414642
- 7468731
- 7468732
- 7468745
- 7468746
- 7468741
- 7468742
- 7468743
- 7468744
- 7468771
- 7468769
- 7468770
- 7468773
- 7468774
- 7468775
- 7482179
- 7482180
- 7482181
- 7482182
- 7482183
- 7482184
- 7482185
- 7482186
- 7468772
- 7482154
- 7482155
- 7482156
- 7482157
- 7468801
- 7468804
- 7468805
- 7468806
- 7482136
- 7468802
- 7468803
- 7482132
- 7482134
- 7482135
- 7482137
- 7482159
- 7482158
- 7482160
- 7482161
- 7495593
- 7495594
- 7495596
- 7495597
- 7495598
- 7495599
- 7482212
- 7495600
- 7495601
- 7495602
- 7495603
- 7495604
- 7495605
- 7495606
- 7495607
- 7495608
- 7495635
- 7495636
- 7495637
- 7495638
- 7495639
- 7495640
- 7495641
- 7495642
- 7495643
- 7495666
- 7495644
- 7495664
- 7482213
- 7495667
- 7503597
- 7503598
- 7503599
- 7503659
- 7510140
- 7510141
- 7510142
- 7503600
- 7503601
- 7517716
- 7517708
- 7503627
- 7503628
- 7503630
- 7503631
- 7503632
- 7503633
- 7503629
- 7503664
- 7503657
- 7503662
- 7503663
- 7503602
- 7503624
- 7510156
- 7517703
- 7517704
- 7517706
- 7517707
- 7517709
- 7517710
- 7517711
- 7517712
- 7517714
- 7517715
- 7408817
- 7411797
- 7411798
- 7411799
- 7411800
- 7414643
- 7414644
- 7414645
- 7414646
- 7414647
- 7414648
- 7414649
- 7417938
- 7417940
- 7417942
- 7417944
- 7417946
- 7417948
- 7417950
- 7417952
- 7417955
- 7417957
- 7417959
- 7503625
Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the Codman Microsensor Basic Kit
- UDI-DI
- 10381780514473
- Lot code
- 7288007
- 7288040
- 7294017
- 7305988
- 7305989
- 7305990
- 7305991
- 7307683
- 7325489
- 7336088
- 7336089
- 7336090
- 7305992
- 7346223
- 7391752
- 7391751
- 7406650
- 7406651
- 7406652
- 7408825
- 7408826
- 7408827
- 7456174
- 7456175
- 7456176
- 7456179
- 7478039
- 7478040
- 7480073
- 7480072
- 7482162
- 7503704
- 7507495
- 7503608
- 7510153
- 7510155
- 7510154
- 7534856
- 7535008
- 7535009
- 7411809
Recall details
- Company began the recall
- Sold in
Worldwide - US Nationwide distribution in the states of Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas Utah, Virginia Washington and the countries of Argentina, Australia, Austria, Bangladesh, Belgium, Bolivia (Plurinational State of), Brazil, Canada, Chile, China, Colombia, Cyprus, Czechia, France, Georgia, Germany, Greece, Hong Kong, Iceland, India, Ireland, Israel, Italy, Japan, Kenya, Korea (the Republic of), Lithuania, Nepal, New Zealand, Poland, Portugal, Romania, Saudi Arabia, Singapore, Slovenia, South Africa, Spain, Sweden, Taiwan (Province of China), Thailand, Turkey, United Arab Emirates (the), United Kingdom of Great Britain and Northern Ireland (the).
- Company
- Integra LifeSciences Corp. (NeuroSciences)Princeton, New Jersey
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98091
- Recall numbers
- Z-1036-2026 to Z-1037-2026
All recalls from Integra LifeSciences Corp. (NeuroSciences)
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
