Mindray DS USA, Inc. dba Mindray North America recalls Hardware configuration of the BeneVision Central Monitoring System (CMS), marketed as BeneVision Distributed…
When the Worstation of the BeneVision DMS has a specific hardware configuration, the computer may experience audio playback failure or screen freezing.
Read the official notice →- Date
- 2025-12-24
- Country
- United States
- Brand
- Mindray DS USA, Inc. dba Mindray
- Product
- Hardware configuration of the BeneVision Central Monitoring System (CMS), marketed as BeneVision Distributed Monitoring System (DMS).…
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide and the country of Canada.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Mindray DS USA, Inc. dba Mindray recalls
- 2025-12-03
USMindray DS USA, Inc. dba Mindray North America recalls Sevoflurane (SEVO) V90 Electronic Vaporizer with the A9 Anesthesia System. Labeled as the following: 1. Sev…
Potential for anesthesia leakage.
FDA · DeviceMindray DS USA, Inc. dba Mindray North AmericaWorldwide - US Nationwide distribution in the states of California, Florida,…Official notice →- 2025-10-01
- US
Mindray DS USA, Inc. dba Mindray North America recalls BeneVision N1 Patient Monitor (N1). Part Numbers: 6660E-PA00017, 6660E-PA00014, 6660E-PA00012, 6660E-PA00011,…
Potential for activation of an abnormal alarm pause.
FDA · DeviceMindray DS USA, Inc. dba Mindray North AmericaWorldwide - Nationwide distribution and the country of Canada.Official notice → - 2024-09-11
- US
Mindray DS USA, Inc. dba Mindray North America recalls Sevoflurane E_Vap.(Safety Filling adapter) used with the A9 Anesthesia System-Used to provide the vapor of an…
V90 electronic vaporizer anesthetic agent output may be higher than the set amount due to a component within the vaporizer causing an incomplete seal in some cases. Should this issue occur, the A9 Anesthesia System…
FDA · DeviceMindray DS USA, Inc. dba Mindray North AmericaUS Distribution to states of: California, Georgia, Kentucky, Mississippi, New…Official notice →
Other drugs & medical recalls in the United States
- 2025-12-24
- US
AVID Medical, Inc. recalls Halyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01.
Potential for incomplete seal on header bag.
- US
Zimmer Surgical Inc recalls Zimmer Air Dermatome, Model/Catalog Number: 00880100100
The devices may have a misaligned thickness control bar.
FDA · DeviceZimmer Surgical IncDistribution regions: USA, Hong Kong, Thailand, Japan, Korea, Australia,…Official notice → - US
Medline Industries, LP recalls SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000
The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.
FDA · DeviceMedline Industries, LPUS Nationwide distribution in the states CA, CO, IL, KS, and MI.Official notice → - US
GE Medical Systems China Co., Ltd. recalls GE Healthcare Carestation anesthesia system, product number and REF numbers: Carestation 610 A1, REF 1012-9620-222;…
Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is unplugged or in the event of an AC mains power failure. Anesthesia…
FDA · DeviceGE Medical Systems China Co., Ltd.Worldwide distribution: US (nationwide) and OUS (foreign) to countries of:…Official notice → - US
Fresenius Kabi USA, LLC recalls Ivenix Infusion System (IIS), LVP Software LVP-SW-0005. Software for the controlled administration of fluids to patients.
Software version 5.10.1 and earlier contain anomalies that have the potential to cause serious patient harm or death.
FDA · DeviceFresenius Kabi USA, LLCUS (Domestic) distribution: CA, CO, FL, GA, ID, IL, MD, MI, MN, MS, NE, NJ,…Official notice → - US
SUN PHARMA /TARO recalls Ciclopirox Shampoo, 1%, 120 mL, Rx only, Mfg by: Taro Pharmaceuticals Inc., Ontario, Canada; Dist. by: Taro Pharmaceuticals USA, Inc., NY…
Failed Impurity/Degradation specifications: OOS results obtained at the 18-month timepoint