Drugs & medicalClass II

Integra LifeSciences Corp. (NeuroSciences) recalls Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN MICROSENSOR Basic Kit is indicated when…

Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits.

Read the official notice →
Date
2026-01-14
Country
United States
Brand
Integra LifeSciences
Product
Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN MICROSENSOR Basic Kit is indicated when direct ICP monitoring is…
Classification
Class II
Units
Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO,…
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Integra LifeSciences recalls

  1. 2026-04-29
  2. US
    Drugs & medicalClass II

    Integra LifeSciences Corp. (NeuroSciences) recalls CUSA Clarity C7000 Console, Software Version: 2.1.1.909. Ultrasonic surgical aspirator system.

    Software issue that renders the touch screen unresponsive.

    FDA · DeviceIntegra LifeSciences Corp. (NeuroSciences)Worldwide - US Nationwide distribution in the states of MI & NY. The countries…Official notice →
  3. 2026-04-22
  4. US
    Drugs & medicalClass II

    Integra LifeSciences Corp. (NeuroSciences) recalls Cytal Burn Matrix 10x15 cm. Product ID: BMM1015.

    Increased rate of out-of-specification endotoxin results.

    FDA · DeviceIntegra LifeSciences Corp. (NeuroSciences)US Nationwide distribution in the states of AL, AZ, CA, DC, FL, GA, IA, IL,…Official notice →
  5. 2026-02-25
  6. US
    Drugs & medicalClass II

    Integra LifeSciences Corp. (NeuroSciences) recalls MediHoney Gel with Active Leptospermum Honey. Model/Catalog Numbers: (1) 31805, (2) 31815. MediHoney Gel dressing…

    Potential packaging failures, which could lead to a breach in the sterile barrier.

    FDA · DeviceIntegra LifeSciences Corp. (NeuroSciences)Worldwide - US Nationwide distribution in the states of TX, MI, FL, IN, MO,…Official notice →
  7. 2025-11-12
  8. US
    Drugs & medicalClass II

    Integra LifeSciences Corp. (NeuroSciences) recalls TruDi¿ Navigation System - Multi Instrument Adapter; - Manufacturer's Product Number (Catalog Number): EM-2025-000F…

    It was determined that when the navigation system is configured with specific revision combinations of the Multi Instrument Adapter together with the Patient Tracker the system may not meet its specified accuracy for…

    FDA · DeviceIntegra LifeSciences Corp. (NeuroSciences)US Nationwide distribution.Official notice →
  9. US
    Drugs & medicalClass I

    Integra LifeSciences Corp. (NeuroSciences) recalls CODMAN Disposable Perforator 11mm. Cranial Perforator.

    Expansion of recall of size 14 mm Codman Disposable Perforators for inadequate welds to size 11 mm and 9 mm Codman Disposable Perforators out of an abundance of caution.

    FDA · DeviceIntegra LifeSciences Corp. (NeuroSciences)Worldwide distribution - US Nationwide and the countries of Argentina,…Official notice →
  10. 2025-09-10
  11. US
    Drugs & medicalClass II

    Integra LifeSciences Corp. (NeuroSciences) recalls Brand Name: MediHoney ¿ Product Name: MediHoney¿ Paste Model/Catalog Number: 31505 Product Description: MediHoney¿…

    Packaging failures were identified which could lead to a breach in the sterile barrier.

    FDA · DeviceIntegra LifeSciences Corp. (NeuroSciences)Worldwide - US Nationwide distribution including in the states of AK, AL, AR,…Official notice →
All 33 Integra LifeSciences recalls →

Other drugs & medical recalls in the United States

  1. 2026-01-21
  2. US
    Drugs & medicalClass II

    Advanced Pharmaceutical Technology, Inc. recalls TESTO-100 CIII (testosterone 100 mg), 10 Sterile Pellets per carton, Rx only, Manufactured by: Advanced Pharmaceutical…

    Lack of Assurance of Sterility: Potential microbial contamination of subcutaneous pellets.

    FDA · DrugAdvanced Pharmaceutical Technology, Inc.GA, NY, TX, Puerto Rico, United Kingdom, Malta, GreeceOfficial notice →
  3. US
    Drugs & medicalClass III

    SUN PHARMACEUTICAL INDUSTRIES INC recalls Clindamycin Phosphate USP, 1% (10 mg/mL), Topical Solution, 60 mL per applicator bottle, Rx only, Mfd. by: Taro Pharmaceutical…

    Failed Impurities/Degradation: Out of Specification results for Total Impurities and for Assay.

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCNationwide in the USA.Official notice →
  4. US
    Drugs & medicalClass III

    SUN PHARMACEUTICAL INDUSTRIES INC recalls Fluocinolone Acetonide Solution Topical Solution USP, 0.01%, 60-mL bottles, Rx only, Dist. by: Taro Pharmaceuticals Inc.,…

    Failed Impurities/Degradation Specifications: Out of specification result was obtained for the known impurity D.

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCNationwide within the USAOfficial notice →
  5. 2026-01-14
  6. US
    Drugs & medicalClass II

    Medline Industries, LP recalls Medline Hudson RCI Medium Concentration Oxygen Masks: 1041CE MASK,OXYGEN,UND CHIN,MED CO OUS ONLY; HUD1035 O2 MASK,MED CONC,SHORT,PEDI,7'…

    Firm received multiple complaints regarding tubing disconnecting from oxygen mask. If issue occurs during use, may lead to delay in patient care and patient may experience shortness of breath leading to hypoxia, which…

    FDA · DeviceMedline Industries, LPWorldwide distribution - US Nationwide and the countries of Australia,…Official notice →
  7. US
    Drugs & medicalClass II

    IMRIS Imaging Inc recalls Brand Name: HFD100 Product Name: Head Fixation Device HFD100 Model/Catalog Number: 119695-000, 119629-000, 119630-000, 113803-000,…

    Torque screw may crack or separate. If used, an affected screw could lead to inadequate head stabilization, compromised surgical precision, procedural delays, requirement for alternate head fixation methods, and risk…

    FDA · DeviceIMRIS Imaging IncWorldwide distribution - US Nationwide and the countries of Canada, Sweden,…Official notice →
  8. US
    Drugs & medicalClass II

    Philips North America Llc recalls Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor.

    It was found that the MX40 device could not reconnect to the PIC iX when moving between Radiohead and Trident 1.4 GHz access points if the signal strength changed quickly.

    FDA · DevicePhilips North America LlcUS Nationwide distribution.Official notice →
See all drugs & medical recalls →