Maquet Cardiopulmonary Gmbh recalls Bubble Sensor for 3/8" x 3/32" tubing; Model Number: 701055720;
Internal investigations have identified an issue with the durability of the connecting cable near the connection to the Venous Bubble Sensor. Excessive bending of the connecting cable can lead to full damage of the…
Read the official notice →- Date
- 2026-02-11
- Country
- United States
- Brand
- Maquet Cardiopulmonary
- Product
- Bubble Sensor for 3/8" x 3/32" tubing; Model Number: 701055720;
- Classification
- Class II
- Units
- Worldwide Distribution: US (Nationwide) and OUS (International) to countries…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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.
More Maquet Cardiopulmonary recalls
- 2026-09-23
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FDA · DeviceMaquet Cardiopulmonary GmbhWorldwide distribution - US Nationwide and the countries of Australia, New…Official notice → - 2025-06-04
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