Mindray 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.
Read the official notice →- Date
- 2025-12-03
- Country
- United States
- Brand
- Mindray DS USA, Inc. dba Mindray
- Product
- Sevoflurane (SEVO) V90 Electronic Vaporizer with the A9 Anesthesia System. Labeled as the following: 1. Sev E_Vap. (Safety Filling…
- Classification
- Class II
- Units
- Worldwide - US Nationwide distribution in the states of California, Florida,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2025-12-24
USMindray 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.
FDA · DeviceMindray DS USA, Inc. dba Mindray North AmericaWorldwide distribution - US Nationwide and the country of Canada.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
- 2025-12-03
- US
Cepheid recalls Xpert MTB/RIF. Model Number: GXMTB/RIF-US-10.
Product testing did not meet expected stability criteria.
- US
INTELERAD MEDICAL SYSTEMS INCORPORATED recalls IntelePACS - InteleConnect / TechPortal
Software application that receives digital images and data to be communicated, processed, manipulated, enhanced, stored, displayed has a bug that could cause data loss in Relevant Clinical Info field when modifying…
FDA · DeviceINTELERAD MEDICAL SYSTEMS INCORPORATEDUS Nationwide distribution in the states of AZ, CT, AL, IL, WA, MD, NJ,CA, TN,…Official notice → - US
DJO, LLC recalls Cold Form Wrap: Back, REF: DP163CT03-BLK-L,XL, and Shoulder, REF: DP163CT02
The IFU (Information for Use) on the wrap instructs the user to heat the hot and cold compression wrap in the microwave for 3 minutes, which may cause the wrap to leak or break at the seams and/or reach temperatures…
FDA · DeviceDJO, LLCUS Nationwide distribution in the states of WI, TN, TX, MD, GA, UT, WA, MI,…Official notice → - US
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion 7M20 systems with FlexArm ceiling-mounted system. Model Number: 722234;
The motorized longitudinal movement of the FlexArm stand may be inconsistent (not smooth) and eventually may become unavailable. This issue is due to grease leakage from the bearings and/or anti-corrosion oil applied…
FDA · DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Domestic: AL, AR, AZ, CA, CO, FL, GA, HI, IL, IN, KS, KY, MD, MN, MO, NM, NY,…Official notice → - US
B Braun Medical Inc recalls Blood Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space…
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
FDA · DeviceB Braun Medical IncWorldwide distribution - US distribution and international distribution to…Official notice → - US
BioFire Diagnostics, LLC recalls BioFire Respiratory Panel 2.1, IVD, REF: 423742 (30 test kit)
Due to unintended movement of pouch chemistry, nucleic acid test may result in elevated risk of false negative results and risk of control failures.
FDA · DeviceBioFire Diagnostics, LLCUS:AZ, FL,GA,ID NC, NH, NJ, NY, OR, PA, SC OUS: NoneOfficial notice →