Recall Atlas
Drugs & medicalClass II

CoreLink LLC recalls CoreLink LLC, FLXFIT 15, 32MM X 8MM, CAGE, REF: AT3208

Specific lots of FLXfit implants have internal components that may have been manufactured using stainless steel rather than the specified titanium alloy.

Read the official notice →
Date
2023-01-18
Country
United States
Brand
CoreLink LLC
Product
CoreLink LLC, FLXFIT 15, 32MM X 8MM, CAGE, REF: AT3208
Classification
Class II
Units
US Nationwide distribution.
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 Details may be shortened or out of date; the official notice is the authoritative source.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.

Other drugs & medical recalls in the United States

  1. 2023-01-25
  2. US
    Drugs & medicalClass I

    Accord Healthcare, Inc. recalls Daptomycin for Injection 350 mg/vial 1 Single-dose vial, Rx only, Manufactured for: Accord Healthcare, Inc., Durham, NC 27703…

    Labeling mixup: cartons labeled as Daptomycin 350 mg/vial were found to contain vials of Daptomycin 500 mg per vial

    FDA · DrugAccord Healthcare, Inc.Nationwide within the United StatesOfficial notice →
  3. US
    Drugs & medicalClass II

    Fresenius Kabi USA, LLC recalls Sensorcaine (Bupivacaine HCl and Epinephrine Injection, USP) with Epinephrine 1:200,000 (as bitartrate), 0.5%, 250 mg per 50 mL (5 mg per…

    Subpotent Drug: Testing results below the defined limit for the epinephrine portion of this product.

    FDA · DrugFresenius Kabi USA, LLCNationwide in the USAOfficial notice →
  4. 2023-01-18
  5. US
    Drugs & medicalClass II

    Covidien, LLC recalls COVIDIEN Emprint Ablation Catheter with Thermosphere Technology, Bronchoscopic Ablation, REF CA108L1

    The product is labeled with the incorrect expiration date.

    FDA · DeviceCovidien, LLCForeign Distribution: Hong KongOfficial notice →
  6. US
    Drugs & medicalClass II

    Medtronic Navigation, Inc. recalls RadiaLux Lighted Retractor (Pink), REF: 50-101-1

    Defect in sterile pouch seal, incomplete seal, of lighted Retractors, increases the risk of contamination, which can lead to post-operative infection.

    FDA · DeviceMedtronic Navigation, Inc.US Nationwide distribution including in the states of OH, CA, FL, NJ, NY, MN,…Official notice →
  7. US
    Drugs & medicalClass II

    Roche Diagnostics Operations, Inc. recalls cobas infinity central lab, Material Number 07154003001

    A complaint investigation revealed that an incorrect behavior relating to the rejection of orders capability of the Host Connectivity Agent (HCA) could occur where the order received from the Laboratory Information…

    FDA · DeviceRoche Diagnostics Operations, Inc.Domestic distribution nationwide. Foreign distribution pending.Official notice →
  8. US
    Drugs & medicalClass II

    Depuy Ireland UC recalls BIOSTOP G BIORESORBABLE CEMENT RESTRICTOR Catalog Numbers: 546308000 (Size 8); 546310000 (Size 10); 546312000 (Size 12); 546314000 (Size…

    All lots of BIOSTOP G Bioresorbable Cement Restrictor are being removed as a precautionary measure because tested endotoxin levels were higher than recommended by the current FDA regulatory guidance. In general,…

    FDA · DeviceDepuy Ireland UCWorldwide distribution - US Nationwide and the countries of Argentina,…Official notice →
See all drugs & medical recalls →