Drugs & medicalClass II

Waters Medical Systems LLC recalls WAVES WCM Kidney Cassette Module

There is a potential for the WCM cassette pump head leaking solution.

Read the official notice →
Date
2022-05-04
Country
United States
Brand
Waters Medical Systems LLC
Product
WAVES WCM Kidney Cassette Module
Classification
Class II
Units
WCM cassettes have been distributed to one domestic customer with two…
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2022-05-04
  2. US
    Drugs & medicalClass II

    Freudenberg Medical, Llc recalls Empower Introducer Sheath with Hydrophilic Coating 21F x 56cm Model: 668782-100 (US)

    Non-intended glue from the hub/shaft bond on the inside ID of the catheter shaft may cause Embolism leading to peripheral ischemia

    FDA · DeviceFreudenberg Medical, LlcUS distribution: GA, OH Foreign distribution: NetherlandsOfficial notice →
  3. US
    Drugs & medicalClass II

    Siemens Healthcare Diagnostics, Inc. recalls IMMULITE 2000 Systems HCG [200 Tests, material number 10381206, catalog number L2KCG] and [600 Tests, material number…

    Potential for falsely elevated hCG results due to sample carryover in serum and urine patient samples, as well as quality control samples and adjustors.

    FDA · DeviceSiemens Healthcare Diagnostics, Inc.Worldwide distribution - US Nationwide distribution in the states of AZ, CA,…Official notice →
  4. US
    Drugs & medicalClass II

    Instrumentation Laboratory recalls ACL TOP 300 CTS/350 CTS/500 CTS/550 CTS/970 CL: Name Part Number 1.ACL TOP 300 CTS 00000280060 2. ACL TOP 300 CTS 00000280060R…

    Updated and revised user instructions issued 7/14/22. Potential carryover issue may cause elevated quality control and sample results for heparin, apixaban or rivaroxaban when HemosIL Liquid Anti-Xa reagent is used in…

    FDA · DeviceInstrumentation LaboratoryWorldwide distribution - US Nationwide and the countries of Argentina,…Official notice →
  5. US
    Drugs & medicalClass II

    Draegar Medical Systems, Inc. recalls Drager Infinity CentralStation Software versions VG2.1.2 and VG2.1.2 SU12. For patient monitoring with Infinity M300 wireless…

    Software issue resulting in temporary loss of central monitoring functionality.

    FDA · DeviceDraegar Medical Systems, Inc.Worldwide distribution - US Nationwide distribution in the states of AL, AR,…Official notice →
  6. US
    Drugs & medicalClass II

    Stryker GmbH recalls Smart Toe II Intramedullary Arthrodesis Implant

    The nickel-sensitivity statement on the outer carton may be partially covered by a label resulting in the statement showing "Indicated for patients with Nickel sensitivity" instead of "Not Indicated for patients with…

    FDA · DeviceStryker GmbHWorldwide distribution - US Nationwide and the countries including Australia,…Official notice →
  7. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc. recalls Acuson 9vE4 Transducer, Model (240)11289564 CE0129, Rx Only ,

    Transducers (component of ultrasound system) may exceed recommended thermal index limits

    FDA · DeviceSiemens Medical Solutions USA, Inc.Worldwide distribution - US Nationwide distribution in the states of…Official notice →
See all drugs & medical recalls →