Integra LifeSciences Corp. (NeuroSciences) 2026-01-14 Health serious FDA
Health · FDA · Recall #FDA-Z-1036-2026
Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN MICROSENSOR… Recall
Issued January 14, 2026 · Integra LifeSciences Corp. (NeuroSciences)
In January 2026, Integra LifeSciences Corp. (NeuroSciences) recalled the Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN MICROSENSOR…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits.
What you should do
- 1 Stop using Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN MICROSENSOR… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Integra LifeSciences Corp. (NeuroSciences) to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Integra LifeSciences Corp. (NeuroSciences)
- Category
- Health
- Recall date
- January 14, 2026
- Units affected
- Not reported
- Sold at
- Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME,
- Recall number
- FDA-Z-1036-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Integra LifeSciences Corp. (NeuroSciences) has 3 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.