Safety Information
The following documents are summary of some medical device safety information related to potentially hazardous cases. It only serves as a quick reference and in no way should be considered as exhaustive and up-to-date. Please refer to the source of information and your product supplier for details.
Listing of Recalls
- RECALL: Voluntary Recall of Clear & Simple Digital Pregnancy Test
- RECALL : Voluntary Recall Of Durex Real Feel Batch
- RECALL: Voluntary Recall of Limited Number of ACUVUE® Brand Contact Lenses
- RECALL: RESPIRONICS TRILOGY 100 VENTILATORS
- RECALL: ALL UNIMPLANTED Cochlear Nucleus CI500 cochlear implant range
Listing of Field Safety Notice
- Jun 2021 : Respironics CPAP and Bi-Level Devices - Sound Abatement Foam Susceptibility to Degradation and Volatile Organic Compound Emission
- ALERT: NIKKISO AQUARIUS SYSTEM – MACHINE’S WHEEL – AQUARIUS HEMOFILTRATION DEVICE
- ALERT: Thermo Fisher Scientific’s – THERMO SCIENTIFIC HM355S-3
- Alert: Omnifuse and Omnifuse PCA Syringe Pumps (“Omnifuse Pumps”)
- ALERT: Fisher & Paykel Healthcare SleepStyle Series CPAP – Power Cord
