Drugs & medicalClass I

Qapel Medical Inc. recalls Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration Tubing, REF: APT6072-132. Hippo 072 Aspiration System including…

Aspiration catheter distal tip features and characteristics may not be in the scope of FDA clearance; tip detachment, vessel rupture, and vasospasm could occur.

Read the official notice →
Date
2025-04-16
Country
United States
Brand
Qapel Medical Inc.
Product
Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration Tubing, REF: APT6072-132. Hippo 072 Aspiration System including…
Classification
Class I
Units
US: CA, IL, NE, TN, TX, NJ, NC, SD, FL, MI, PA, GA, AL, IN, NY, WI, AZ, MN,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2025-04-16
  2. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls Wayson Hydrocolloid Models: 1) MJ BANDAGE HYDROCOLLOID HEEL OVAL 6CT, Model Number: MJ18004V2; 2) MJ BANDAGE HYDROCOLLOID…

    There is a potential for the sterility of the device to be compromised.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldWorldwide Distribution: US (Nationwide) and OUS (Foreign) to countries of:…Official notice →
  3. US
    Drugs & medicalClass II

    Beckman Coulter, Inc. recalls DxI 9000 Access Immunoassay Analyzer, catalog number C11137 in vitro diagnostic device used for the quantitative, semi-quantitative, or…

    Ground screws on Dxl 9000 PCB boards may cause electric shorts, leading to smoke and potentially delaying patient results. Smoke also poses a hazard to equipment and users.

    FDA · DeviceBeckman Coulter, Inc.OUS (Foreign) distribution to countries of: Australia, Croatia, Czechia,…Official notice →
  4. US
    Drugs & medicalClass II

    BioFire Diagnostics, LLC recalls FilmArra Pneumonia Panel plus (Pneumoplus), REF: RFIT-LBL-0374

    Increased risk of control failures and false negative test results with multiplexed nucleic acid test.

    FDA · DeviceBioFire Diagnostics, LLCOUS International Distribution to countries of: France, Italia, Spain,…Official notice →
  5. US
    Drugs & medicalClass I

    MEDLINE INDUSTRIES, LP - Northfield recalls Medline medical convenience kits labeled as: 1) NEONATAL INTUBATION TRAY, REF ACC010371C; 2) NEWBORN RESUSCITATION KIT, REF…

    Specific Medline Kits were manufactured using Intubation ORAL/NASAL Endotracheal Tubes which were subsequently recalled by Smiths Medical.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldCaliforniaOfficial notice →
  6. US
    Drugs & medicalClass I

    MEDLINE INDUSTRIES, LP - Northfield recalls Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: TOL DR R PACK

    Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS: CA, FL, MN, NY, OH, OR, PA, TX, WVOfficial notice →
  7. US
    Drugs & medicalClass I

    MEDLINE INDUSTRIES, LP - Northfield recalls Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: CABG OPNHRT S HSP, CARDIAC…

    Medline medical procedure kits, containing Medtronic Aortic Root Cannula

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS: CA, FL, MN, NY, OH, OR, PA, TX, WVOfficial notice →
See all drugs & medical recalls →