Drugs & medicalClass II

Philips North America Llc recalls Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703A

Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker output.

Read the official notice →
Date
2026-07-01
Country
United States
Brand
Philips
Product
Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703A
Classification
Class II
Units
Worldwide distribution - US Nationwide and The countries of AE, AT, AU, BE,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Philips recalls

  1. 2026-09-09
  2. US
    Drugs & medicalClass II

    Philips North America Llc recalls Philips Brilliance CT 64: Brilliance CT 64 Channel Product Code: 728231, Brilliance CT 64 Upgrades Product Code: 728232. Software…

    Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the equipment.

    FDA · DevicePhilips North America LlcUS and US Territories.Official notice →
  3. 2026-08-26
  4. US
    Drugs & medicalClass II

    Philips North America Llc recalls Cardiac Workstation 5000. Product Number: 860439.

    Device will intermittently provide inaccurate data related to native heart rate.

    FDA · DevicePhilips North America LlcWorldwide distribution - US Nationwide and the countries of Australia,…Official notice →
  5. 2026-07-01
  6. US
    Drugs & medicalClass II

    Philips North America Llc recalls Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232. Includes the following system descriptions: TELE Monitor 5500, 1.4 Ghz,…

    Potential for device reset to default "NEW_DEVICE" state, which may lead to a to loss of device configuration and the equipment label, resulting in a failure to reconnect to the PIC iX central monitoring system.

    FDA · DevicePhilips North America LlcUS Nationwide distribution in the states of AZ, CA, CO, IN, MA, MI, MN, PA,…Official notice →
  7. 2026-06-17
  8. US
    Drugs & medicalClass II

    Philips North America Llc recalls DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.

    System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.

    FDA · DevicePhilips North America LlcUS distribution to California.Official notice →
  9. 2026-05-06
  10. US
    Drugs & medicalClass II

    Philips North America recalls Philips SmartPath to dStream for 3.0T with MR Elastography (MRE). 1. Model Number (REF): 782145.

    The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE…

    FDA · DevicePhilips North AmericaWorldwide - US Nationwide and the countries of Argentina, Australia,…Official notice →
  11. 2026-02-18
  12. US
    Drugs & medicalClass II

    Philips North America Llc recalls Brilliance iCT; Product Code (REF): 728306;

    As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to specification. If multiple fasteners…

    FDA · DevicePhilips North America LlcWorldwide - US Nationwide distribution in the states of AL, AR, CA, CO, CT,…Official notice →
All 100 Philips recalls →

Other drugs & medical recalls in the United States

  1. 2026-07-01
  2. US
    Drugs & medicalClass II

    PFM MEDICAL INC. recalls Multi-Snare Set: 5 mm x 125 cm, REF: 147305; 10 mm x 125 cm, REF: 147310

    A snare catheter including luer lock, indicated for removal or manipulation of a foreign body in the vascular system, failed to meet the biocompatibility requirements for in-vitro-cytotoxicity, which if in contact with…

    FDA · DevicePFM MEDICAL INC.US Nationwide distribution in the states of NY, MD.Official notice →
  3. US
    Drugs & medicalClass II

    Ventec Life Systems, Inc. recalls VOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-001

    Respiratory system intended to provide continuous/intermittent ventilator support, may have a damaged back-up battery supporting backup alarm function, which may result in the backup alarm not activating during loss of…

    FDA · DeviceVentec Life Systems, Inc.US Nationwide distribution in the state of UT.Official notice →
  4. US
    Drugs & medicalClass II

    TMJ Solutions Inc recalls TMJ Bilateral Implants, REF: CHG020

    Custom temporomandibular joint implant may have contained incorrect patient-specific components that led to a poor fit of the implant, leading to a right-sided open bite.

    FDA · DeviceTMJ Solutions IncUS Nationwide distribution in the state of MA.Official notice →
  5. US
    Drugs & medicalClass II

    Intuitive Surgical, Inc. recalls Da Vinci ASSY, PSS, SP1098, Part Number: 380601

    Operative components of surgical systems potentially distributed with E-brake retainer pin, so in event of a structural column failure, the E-brake pin would prevent E-brake engagement and may result in uncontrolled…

    FDA · DeviceIntuitive Surgical, Inc.Worldwide - US Nationwide distribution including in the states of CA, GA, OH,…Official notice →
  6. US
    Drugs & medicalClass I

    Medline Industries, LP recalls Medline Convenience Kits: 1) DYNJ905503F, Model Number: CV ANESTHESIA - ROOM SET UP; 2) DYNJ905503G, Model Number: CV ANESTHESIA - ROOM…

    The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified…

    FDA · DeviceMedline Industries, LPUS Nationwide.Official notice →
  7. US
    Drugs & medicalClass II

    SUN PHARMACEUTICAL INDUSTRIES INC recalls Perampanel CIII Tablets, 6mg, Rx only, 30 Tablets, Mfd.by: Taro Pharmaceutical Industries Ltd., Haifa Bay, Israel 2624761,…

    Labeling: Label Mix-up: 10mg Perampanel CIII tablet was found in a Perampanel CIII bottle labeled Perampanel 6 mg tablets.

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCNationwide in the USAOfficial notice →
See all drugs & medical recalls →