Drugs & medicalClass II

Jinan Bodor Cnc Machine Co Ltd recalls Bodor P and C series laser cutting machines

Non-compliant laser products

Read the official notice →
Date
2025-01-29
Country
United States
Brand
Jinan Bodor Cnc Machine
Product
Bodor P and C series laser cutting machines
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 Details may be shortened or out of date; the official notice is the authoritative source.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.

More Jinan Bodor Cnc Machine recalls

  1. 2025-07-30
  2. US
    Drugs & medicalClass II

    Jinan Bodor Cnc Machine Co Ltd recalls Bodor's I series laser cutting machine.

    The Bodor i Series products fail to meet certain applicable Federal standards, 21 CFR 1040.10(f)(1) and 21 CFR 1040.10(f)(2).

    FDA · DeviceJinan Bodor Cnc Machine Co LtdUSOfficial notice →
All 2 Jinan Bodor Cnc Machine recalls →

Other drugs & medical recalls in the United States

  1. 2025-01-29
  2. US
    Drugs & medicalClass II

    CareFusion 303, Inc. recalls BD Pyxis Med ES Auxiliary (AUX), REF 343

    Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure,…

    FDA · DeviceCareFusion 303, Inc.WorldwideOfficial notice →
  3. US
    Drugs & medicalClass II

    Adept Medical Ltd recalls Otological Ventilation Tube - T-Tube 9mm - Silicone; Product Code: NZ3309;

    Lack of 510(k) clearance.

    FDA · DeviceAdept Medical LtdUS Nationwide distribution. International: Canada, New Zealand, Australia,…Official notice →
  4. US
    Drugs & medicalClass I

    Percussionaire Corporation recalls VDR4 Phasitron Breathing Circuit Models that contain the venturi component: -A50094 D 5PK, Phasitron Kit, VDR, Single Patient, 5pk…

    Due to internal venturi component getting transiently stuck in the forward position within the breathing circuit and may cause a reduction of amplitude and volume of ventilation.

    FDA · DevicePercussionaire CorporationWorldwide - U.S. Nationwide distribution in the states of AZ, FL, IL, MS, MO,…Official notice →
  5. US
    Drugs & medicalClass III

    Appco Pharma LLC recalls Venlafaxine Extended-Release Tablets, 150mg, Rx only, 90 Tablets, Manufactured by Appco Pharma. LLC, NDC 43598-943-90.

    Failed Tablet/Capsule Specifications: Missing tab ID on either side of the tablet

    FDA · DrugAppco Pharma LLCNationwide USA.Official notice →
  6. US
    Drugs & medicalClass I

    SHOPPERS- PLAZA recalls FOUZEE SugarLin HERBAL FORMULA capsules, 180 capsules per bottle, Sold and Distributed by Shoppers-Plaza, Hawthorne, CA 90250. Product of…

    Marketed without an Approved NDA/ANDA; FDA laboratory analysis confirmed product tainted with undeclared metformin and glyburide

    FDA · DrugSHOPPERS- PLAZANationwide via internet salesOfficial notice →
  7. US
    Drugs & medicalClass II

    First Aid Beauty Ltd recalls First Aid Beauty Ultra Repair Cream, colloidal oatmeal 0.5%, Coconut Vanilla, Net Wt. 396.8 g (14 OZ), DISTR. BY: First Aid Beauty LTD,…

    CGMP Deviations; product intended for quarantine was inadvertently distributed

    FDA · DrugFirst Aid Beauty LtdNationwideOfficial notice →
See all drugs & medical recalls →