Drugs & medicalClass II

Deerfield Imaging, Inc. recalls Operating room table - Product Usage: intended for use during diagnostic examinations, radiologic procedures or surgical procedures to…

ORT200/300 rotational lock may fail to function such that it cannot change states between locked and unlocked, due to a mechanical hardware issue.

Read the official notice →
Date
2021-10-06
Country
United States
Brand
Deerfield Imaging
Product
Operating room table - Product Usage: intended for use during diagnostic examinations, radiologic procedures or surgical procedures to…
Classification
Class II
Units
Worldwide distribution - US Nationwide distribution FL, NH, TX, OH, CA, OR,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Deerfield Imaging recalls

  1. 2022-04-20
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    Deerfield Imaging, Inc. recalls Trumpf Mount Clamp Assembly (table adapter component), part #118704-000, a component of the IMRIS HFD100 head fixation device, models…

    Reports have been received that after normal or routine lateral forces are applied to the head fixation device, the split block clamp may deflect (rotationally around the axis) and not return to within acceptable…

    FDA · DeviceDeerfield Imaging, Inc.Worldwide distribution - US Nationwide distribution in the states of AL, FL,…Official notice →
All 2 Deerfield Imaging recalls →

Other drugs & medical recalls in the United States

  1. 2021-10-06
  2. US
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    Atrium Medical Corporation recalls Atrium ADVANTA VXT Vascular Graft, Part No. 22059, UDI 00650862220599 - Product Usage: intended for use in arterial vascular…

    The product package may potentially contain a mismatched graft that does not contain the radial support ring (helix) identified in the labeling.

    FDA · DeviceAtrium Medical CorporationWorldwide distribution - US Nationwide distribution in the state of Florida…Official notice →
  3. US
    Drugs & medicalClass II

    ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Arjo Citadel beds originally assembled with the IndiGo modules during manufcturing, model number CX812A3J3AMAD0; and IndiGo…

    The IndiGo power cord might wear during use which could lead to its damage, resulting in the cord being cut, burnt or short circuit with limited emission of sparks.

    FDA · DeviceARJOHUNTLEIGH POLSKA Sp. z.o.o.US Nationwide distribution in the states of CA, FL, IL, KY, MD, NV, NY, PA,…Official notice →
  4. US
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    Vero Biotech, LLC recalls GENOSYL DS (Delivery System) console, for use as a vasodilator.

    Manufacturing defect involving reversal of the inlet and outlet gas lines, resulting in delivery of nitrogen dioxide (NO2) instead of nitric oxide (NO).

    FDA · DeviceVero Biotech, LLCDistributed within US to Texas and Illinois.Official notice →
  5. US
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    North Coast Medical Inc recalls EcoLotion Transmission Lotion, used in ultrasound procedures. Item/Description: NC70481/Eco Lotion 5 liters, NC70482/Eco Lotion with Aloe…

    Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. On August 18, 2021, FDA published a Letter to Health Care Providers to further address this issue:…

    FDA · DeviceNorth Coast Medical IncWorldwide distribution. US nationwide, Canada, Israel, South Africa,…Official notice →
  6. US
    Drugs & medicalClass II

    Biodex Medical Systems, Inc. recalls Atomlab 500 Dose Calibrator Software 2.0.00 through Revision 2.0.08, inclusive Model: 086-330.

    When deleting a previously entered custom isotope, the software deletes the isotope, but not the associated dial setting. Possible other stored custom isotopes may then have incorrect dial settings and may lead to an…

    FDA · DeviceBiodex Medical Systems, Inc.Nationwide Foreign: Austria Autralia Brazil CANADA Chile Colombia Croatia…Official notice →
  7. US
    Drugs & medicalClass II

    Aesculap Implant Systems LLC recalls PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM Catalog Number: FC700SU

    Malfuncton-Implant did not deploy successfully may necessitate the need for an additional medical intervention for patients which would result in a potential delay in surgery

    FDA · DeviceAesculap Implant Systems LLCUS Nationwide distribution in the states of FL, MI, NY, TX, WI.Official notice →
See all drugs & medical recalls →