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).

Read the official notice →
Date
2025-07-30
Country
United States
Brand
Jinan Bodor Cnc Machine
Product
Bodor's I series laser cutting machine.
Classification
Class II
Units
US
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2025-01-29
  2. US
    Drugs & medicalClass II

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

    Non-compliant laser products

    FDA · DeviceJinan Bodor Cnc Machine Co LtdUS Nationwide DistributionOfficial notice →
All 2 Jinan Bodor Cnc Machine recalls →

Other drugs & medical recalls in the United States

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

    MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: 1) BLOOD CULTURE KIT, REF DYNDH1462B;…

    Affected convenience kits contain BD ChloraPrep Clear - 1 mL Applicators, which were recalled by BD due to potential to exhibit an open seal on its packaging. This may constitute a breach to sterility, which may in…

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldDistributed domestically to California, Florida, Pennsylvania, and Texas. No…Official notice →
  3. US
    Drugs & medicalClass II

    Beckman Coulter Inc. recalls Estrone RIA, REF: DSL8700. Estrone RIA is an IVD used for the quantitative measurement of estrone in human serum and plasma.

    A specific lot of bovine serum albumin (BSA) used for manufacturing of coated tubes (CT) that are included in the Estrone RIA kit lots caused different affinity of manufactured coated tubes to patient samples, causing…

    FDA · DeviceBeckman Coulter Inc.US: North Carolina OUS: Argentina, Austria, Belgium, Canada, France, Germany,…Official notice →
  4. US
    Drugs & medicalClass II

    Covidien recalls Covidien Nellcor Bedside SpO2 Patient Monitoring System: REF: PM100N, 10005941, DLPM100N, DL10005941, DSPM100N, 10005941-SG, DS10005941,…

    Bedside SpO2 Patient Monitoring System alarms not heard/recognized, resulting in: treatment delay, lack of low oxygen saturation response, respiratory failure, arrhythmia. Highlighting operator's manual: 1)For patient…

    FDA · DeviceCovidienWorldwide - US Nationwide distribution including in the states of MS, TX, FL,…Official notice →
  5. US
    Drugs & medicalClass II

    Encore Medical, LP recalls Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD40 Model/Catalog Number:…

    Due to packaging discrepancy with the incorrect tibial inserts/implants being packaged. Issued discovered via a customer complaint.

    FDA · DeviceEncore Medical, LPRFK Medical Inc. Viriginia (VA) CE102 952-28-40E 2224A1124A EMPOWR Acetabular,…Official notice →
  6. US
    Drugs & medicalClass II

    Olympus Corporation of the Americas recalls Ellik Evacuator. Model Number: 194. The Ellik Evacuator and adapter accessories are compatible with Gyrus ACMI Elite and…

    Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).

    FDA · DeviceOlympus Corporation of the AmericasInternational distribution to the country of Japan.Official notice →
  7. US
    Drugs & medicalClass II

    Natus Neurology DBA Excel Tech., Ltd. (XLTEK) recalls Natus Brain Monitor Breakout Box, Part Number 021911; full-montage standard electroencephalograph

    Natus received two complaints of left side labeling show impedance for right side.

    FDA · DeviceNatus Neurology DBA Excel Tech., Ltd. (XLTEK)US: CA, IN, MO, NC, PA, RI, TXOfficial notice →
See all drugs & medical recalls →