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Other Medical Devices

🏥 Medical Devices 15,809 recalls

Class I - Dangerous

There is a risk of mis-association of patient demographic data for users who choose to report results manually when their Service Control Unit (SCU) is operating near capacity and are using save actions (Skip, Final Discard, Mark as Read, Save) to process patient results rapidly.

Jun 8, 2023 Other Medical Devices View Details →

Possible out of specification endotoxin test results due to issues with in-process and finished goods endotoxin testing.

May 23, 2023 Other Medical Devices Nationwide View Details →

GE HealthCare has become aware of the potential that an incorrect type of secondary latch could have been installed on the northeast (NE) and/or northwest (NW) bedside panels for certain Giraffe OmniBed and Giraffe OmniBed Carestation devices

May 19, 2023 Other Medical Devices View Details →

Automated dispensing cabinet devices plugged into any multi-socket outlet power strips may present unacceptable levels of current leakage, which could expose users to system downtime and/or potential electric shock.

May 22, 2023 Other Medical Devices Nationwide View Details →

Raw material issue may cause cardiac panel products to have an average of 30% troponin signal reduction across measurement range 0.05 ng/mL to 30 ng/mL, QC testing won't detect anomaly, so an alternate method is recommended, if unavailable, use recommendations to mitigate potential patient impact, which could be missed/delayed myocardial infarction diagnosis.

May 25, 2023 Other Medical Devices Nationwide View Details →
Class I - Dangerous

GE HealthCare has become aware of the potential that an incorrect type of secondary latch could have been installed on the northeast (NE) and/or northwest (NW) bedside panels for certain Giraffe OmniBed and Giraffe OmniBed Carestation devices

May 19, 2023 Other Medical Devices View Details →