"Medical Device Recalls" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Removal of a MEDICAL DEVICE from the market due to a problem occurring in the manufacture or distribution of the product.
| Descriptor ID |
D057052
|
| MeSH Number(s) |
N06.850.210.637.500
|
| Concept/Terms |
Medical Device Recalls- Medical Device Recalls
- Device Recall, Medical
- Device Recalls, Medical
- Medical Device Recall
- Recall, Medical Device
- Recalls, Medical Device
Biomedical Device Recalls- Biomedical Device Recalls
- Biomedical Device Recall
- Device Recall, Biomedical
- Device Recalls, Biomedical
- Recall, Biomedical Device
- Recalls, Biomedical Device
|
Below are MeSH descriptors whose meaning is more general than "Medical Device Recalls".
Below are MeSH descriptors whose meaning is more specific than "Medical Device Recalls".
This graph shows the total number of publications written about "Medical Device Recalls" by people in this website by year, and whether "Medical Device Recalls" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2010 | 0 | 1 | 1 |
| 2017 | 1 | 0 | 1 |
| 2018 | 2 | 0 | 2 |
| 2019 | 0 | 1 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Medical Device Recalls" by people in Profiles.
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Procedural outcomes associated with transvenous lead extraction in patients with abandoned leads: an ESC-EHRA ELECTRa (European Lead Extraction ConTRolled) Registry Sub-Analysis. Europace. 2019 Apr 01; 21(4):645-654.
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Pacemaker Recall Highlights Security Concerns for Implantable Devices. Circulation. 2018 10 09; 138(15):1597-1598.
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Factors Influencing the Decision to Proceed to Firmware Upgrades to Implanted Pacemakers for Cybersecurity Risk Mitigation. Circulation. 2018 09 18; 138(12):1274-1276.
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High Court will hear class action against metal-on-metal hip manufacturer. BMJ. 2017 10 11; 359:j4711.
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The role of the U.S. Food and Drug Administration in device evaluation and monitoring. Gastrointest Endosc. 2010 Jul; 72(1):5-10.