Recall Atlas
Drugs & medicalClass II

Carefree Surgical Specialties recalls Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy Kittner Rolls Gauze Medium 4 Long X-Ray Detectable 5/pk…

Due to two issues: 1. Product contamination (biological foreign matter) that could compromise sterility. 2. Incorrect quantity of gauze in sterile packaging

Read the official notice →
Date
2025-08-20
Country
United States
Brand
Carefree Surgical Specialties
Product
Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy Kittner Rolls Gauze Medium 4 Long X-Ray Detectable 5/pk…
Classification
Class II
Units
US Nationwide distribution in the states of KY, TX, FL, NC, CO, CA, ID, WV,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2025-08-20
  2. US
    Drugs & medicalClass II

    Waldemar Link GmbH & Co. KG (Mfg Site) recalls Prosthesis Head B, 28 mm, 7 mm neck length. Item Number: 198-828/04.

    Inconsistent size terminology and color coding used on labeling

    FDA · DeviceWaldemar Link GmbH & Co. KG (Mfg Site)Worldwide - US Nationwide distribution in the states of AZ, CA, FL, IN, KS,…Official notice →
  3. US
    Drugs & medicalClass II

    Spark Biomedical Inc recalls Sparrow Ascent Patient Controller, REF's: 11-110-K, 11-310-K, 11-320-K, 11-321-K, 11-310-K-28, 11-320-K-28, 11-321-K-28

    Due to manufacturing issue, neurostimulator device may experience "cable disconnect" error message and interruption to stimulation output.

    FDA · DeviceSpark Biomedical IncUS Nationwide distribution.Official notice →
  4. US
    Drugs & medicalClass II

    Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEE INS, 4L 16MM, VE Model/Catalog Number: 341-16-704 Product…

    Knee implants contain incorrect labeling (size and/or side incorrect)

    FDA · DeviceEncore Medical, LPUS Nationwide distribution in the states of AL, AZ, CA, CO, FL, IA, IL, IN,…Official notice →
  5. US
    Drugs & medicalClass II

    SPINEART SA recalls Brand Name: PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model/Catalog Number: MPF-PS 55 45-S Software Version: Not…

    Cannulated fenestrated polyaxial screws may be incorrectly labeled

    FDA · DeviceSPINEART SAUS Nationwide distribution in the states of Florida , Kentucky, California.Official notice →
  6. US
    Drugs & medicalClass II

    Boston Scientific Corporation recalls FARAWAVE 1.0 Pulsed Field Ablation Catheter, Product ID M004PF41M401

    The potentially impacted units were manufactured using specific equipment that may have caused cracks in the electrode bands on the catheter's distal end.

    FDA · DeviceBoston Scientific CorporationUS Nationwide.Official notice →
  7. US
    Drugs & medicalClass I

    Boston Scientific Corporation recalls Carotid WALLSTENT Monorail Endoprosthesis Closed Cell Self-Expanding Stent, stent and stent delivery system. Material numbers:…

    Certain batches are being removed due to an increase in complaints received in which physicians encountered greater than anticipated resistance while attempting to withdraw the stent delivery system (SDS) from the…

    FDA · DeviceBoston Scientific CorporationDomestic US Nationwide distribution including Puerto Rico. International…Official notice →
See all drugs & medical recalls →