- Safety alert
Medical device recalls
A device recall may call for a repair, a software update or new instructions. Identify your exact device, then read what FDA and the manufacturer say to do next.
- Indexed notices
- 64
- Primary sources
- FDA
What this category covers
Glucose monitors, CPAP devices, Test kits, Implants. Home health equipment, test kits and implants, including FDA recalls and early safety alerts.
Check with the official agency or read the product identification guide. Source coverage explains which notices are indexed and when each source was imported.
Recalls & safety alerts
64 indexed notices. Always compare with the current official notice.
FDA
Volara: Volara system single-patient use circuit and blue ventilator adapter assembly
Reports of the handset plug disconnecting from the nebulizer port on the blue ventilator adapter
- Recall
FDA
Baxter: Life2000 Ventilator with an attached battery charger dongle
Potential Battery Charger Dongle Damage
- Recall
FDA
Medline: SubG Endotracheal Tubes with Subglottic Suction and kits that contain these devices
The inflation tube and other device components have become detached and/or torn from the main tube, resulting in moisture buildup, loss of pressure, or inability to inflate.
- Recall
- Recall
- Recall
FDA
Nimbus: Nimbus Pump System
Recall due to a high number (3698) of customer complaints related to the Nimbus Infusion Pump systems
- Safety alert
FDA
Mojo, Mojo 2, iQ 2, Phantom 2: CPAP and BIPAP Masks with Magnets
Potential interference with certain medical implants
- Recall
Read the product identification guide
Official checking resources
- FDA device recalls & early alerts — Serious device recalls, early alerts and updates.
- FDA device recall database — Search the broader database by device, company or recall information.
Data sources & coverage
Official sources may have newer notices or a broader history. See all sources and coverage.