Official recall record
Product REF 4050-100N, DRAIN, EXPRESS BRU W/AC, Blood Recovery Unit
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2023-12-13
- Country of alert
- United States
- Alert level
- Class I
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00650862115147
- Brand on record
- Maquet Cardiovascular, LLC
What the authority reported
Express chest drains are pre-packaged with sterile water syringes which have bene recalled. If the device is not kept in an upright position, the patient may be exposed to infectious material. Subsequent hazards include but are not limited to infection, abscess, sepsis, and death.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
Other recalls from this brand
- 2026-06-02 · US FDA — Medical Devices
The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000; UDI 00607567700406) is a sterile, - 2025-08-06 · US FDA — Medical Devices
Vasoview Hemopro 3 Endoscopic Vessel Harvesting System Model No. C-VH-6000. The VASOVIEW HEMOPRO 3 Endoscopi - 2025-03-20 · US FDA — Medical Devices
The VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System is designed for use in conjunction with the 7 mm ex
All 9 official recall notices naming Maquet Cardiovascular, LLC on this site →
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