Arcoma AB recalls Omnera 400A Digital Radiographic System
There is the potential for the X-Ray system to short circuit due to an ingress of liquid in the display handles which may result in uncontrolled movement of the Overhead Tube Crane (OTC).
Read the official notice →- Date
- 2022-07-13
- Country
- United States
- Brand
- Arcoma AB
- Product
- Omnera 400A Digital Radiographic System
- Classification
- Class II
- Units
- US Nationwide distribution in the states of NM, DE, TX, VT, FL, MO, UT, PA,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- 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
- 2022-07-13
US
Chromsystems Instruments & Chemicals GmbH recalls MassCheck Amino Acid, Acylcarnitines Dried Blood Spot Control Level I
Too low concentration of glycine was detected in the dried blood controls of the batch 2821 of the products.
US
Luminex Corporation recalls VERIGENE Enteric Pathogens Nucleic Acid Test, Part No. 30-002-23
There is a potential for false negative results using VERIGENE CDF Stool PREP KIT and VERIGENE EP Stool PREP KIT due to hydrophobic characteristics of the swab.
FDA · DeviceLuminex CorporationWorldwide distribution - US Nationwide and the countries of Kuwait, Austria,…Official notice →US
GE Healthcare, LLC recalls GE Centricity Universal Viewer Zero Footprint. To view, communicate, process, and display Medical images and data within a computer…
Potential to display inaccurate measurements on images in Centricity Universal Viewer Zero Footprint Client (ZFP)
US
Ossur Americas recalls OSSUR VARIFLEX SUBA JUNIOR foot and ankle external prosthesis, sized for children and adolescents.
Due to receiving complaints related to broken (cracked) prosthetic foot with failures occurring in situations where sudden high impact twisting or bending is applied to the foot.
FDA · DeviceOssur AmericasWorldwide distribution including US nationwide (including Puerto Rico).Official notice →US
DePuy Spine, Inc. recalls EIT CIF cage, H 7mm, 8degree, S- an intervertebral body fusion devices indicated for use with autograft when used as an adjunct to fusion…
Label on the Outer Carton does not match the labels on the Outer Blister package, Inner Blister package and Patient Labels. The only label that may not be correct is on the Outer Carton
US
Covidien, LP recalls EEA Autosuture Circular Stapler with DST Series Technology, 25mm. Model Numbers EEA25, EEAXL25, EEA2535, and EEAXL2535.
The affected staplers have the potential for the staple guide to not be securely attached to the instrument. The issue could cause the component to disengage and if disengaged, could allow the device to transect tissue…