Maquet Medical Systems USA recalls Bubble Sensor (REF: 70105.5720)
The Bubble Sensor optional accessory to the CARDIOHELP-i extracorporeal life support system includes an incorrect UDI Device Identifier (DI) provided with the label attached to the device.
Read the official notice →- Date
- 2024-02-14
- Country
- United States
- Brand
- Maquet Medical Systems
- Product
- Bubble Sensor (REF: 70105.5720)
- Classification
- Class II
- Units
- AZ, CA, CO, FL, GA, IA, IL, MN, NE, PA, TX, WA and WI.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
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