FDA Urges Companies to Be ‘Recall Ready’ to Protect Public Health
The FDA finalized guidance to help companies prepare to quickly and effectively remove violative products from the market.
Read MoreThe FDA finalized guidance to help companies prepare to quickly and effectively remove violative products from the market.
Read MoreMar 2, 2022 | Equipment management, Medical Equipment | 0 |
Ordr’s new connected medical device solution is designed to allow HTM teams to more efficiently and accurately manage their medical devices.
Read MoreFeb 9, 2022 | Recalls, Ventilators | 0 |
ImtMedical, a subsidiary of Vyaire Medical, has initiated a recall of certain Bellavista ventilators, due to a software and configuration issue. The U.S. FDA cleared the BellaVista 1000e ventilator in late 2019.
Read MoreJan 27, 2022 | Recalls, Ventilators | 0 |
Certain Philips ventilators that were recalled last year may lead to injuries or death, according to a new classification of the recall by the FDA.
Read MoreComplications involving a recall for certain sleep and respiratory care devices are causing some to make difficult personal health decisions.
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