Merge Healthcare, Inc. recalls VERICIS, Merge Cardio, Model/Catalog Number: Version 9.x, Software Version: 9.0.6 and 9.0.8; VERICIS is an integrated cardiovascular…
When following a specific less typical workflow in which the user remeasures using the ultrasound device or manually edits primitive or derived measurement values directly in Clinical Reporting, derived measurements…
Read the official notice →- Date
- 2025-03-26
- Country
- United States
- Brand
- Merge Healthcare
- Product
- VERICIS, Merge Cardio, Model/Catalog Number: Version 9.x, Software Version: 9.0.6 and 9.0.8; VERICIS is an integrated cardiovascular…
- Classification
- Class II
- Units
- US
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Merge Healthcare recalls
- 2026-09-02
USMerge Healthcare, Inc. recalls Merge PACS and Merge OrthoPACS, medical imaging diagnostic workstation
Software issue may cause measurements to be displayed inaccurately.
FDA · DeviceMerge Healthcare, Inc.US Nationwide distribution in the states of California, Florida, Kentucky,…Official notice →- 2026-08-12
- US
Merge Healthcare, Inc. recalls Merge PACS, medical imaging diagnostic workstation
Thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open.
FDA · DeviceMerge Healthcare, Inc.Worldwide distribution - US Nationwide and the countries of Canada, and UK.Official notice → - 2025-09-10
- US
Merge Healthcare, Inc. recalls Merge Hemo, Model RCSV2, Model/Catalog Number 99-01172-00, software versions 11.1 and 11.1.1 Product Description: The Merge Hemo, Model…
Merge Healthcare has been informed by Schiller AG (Baar, Switzerland) of an issue with the Schiller ARGUS PB-3000 Patient Data Module (PDM) where certain units trigger an error message on the Merge Hemo Client (…
FDA · DeviceMerge Healthcare, Inc.US Nationwide distribution including in the states of Arizona, Arkansas,…Official notice →
Other drugs & medical recalls in the United States
- 2025-03-26
- US
American Contract Systems Inc recalls CRANI PACK, Model/Catalog Number WECR41D, medical procedure kit.
During an internal investigation, ACS was unable to confirm that the CODMAN component achieved the required Sterility Assurance Level and therefore is not suitable for sterilization according to ACS procedures.
- US
Smiths Medical ASD, Inc. recalls CAPNOCHECK BCI Airway Adapter; Model Number BSR; Product Code WW1100
Airway adapter does not meet specification and may break off when attaching a valve or tube. Device failure may result in inaccurate readings, a break in airway circuit, and loss of ventilation. A break in the airway…
FDA · DeviceSmiths Medical ASD, Inc.US Nationwide distribution. International distribution pending.Official notice → - US
ZIMMER ORTHOPEDICS MANFACTURING LIMITED-GALWAY recalls Comprehensive Shoulder Stem, Comprehensive Micro Stem, Comprehensive Mini Stem; uncemented shoulder prosthesis,…
Five complaints received where surgeon was unable to remove and/or connect the inserter with the stem during surgery due to excess material remaining within the taper. Issue may lead to clinically significant extension…
FDA · DeviceZIMMER ORTHOPEDICS MANFACTURING LIMITED-GALWAYUS distribution nationwide. International distribution to Dominican Republic,…Official notice → - US
B Braun Medical Inc recalls Introcan Safety 3 Closed IV Catheter 22 Ga. x 1 in., PUR, Winged. Passive safety IV catheter.
Increased risk for valve housing detachment causing leakage.
FDA · DeviceB Braun Medical IncDomestic: CA, CA, FL, GA, IL, IL, IN, MD, MN, MO, NC, NM, NY, PA, TN, TX, VA,…Official notice → - US
Remel, Inc recalls Zebra Thermal Barcode Printer GX430t, Model no. YSW 1000 or YSW 2000, may have been sold as an optional accessory for Sensititre Aris HIQ…
Power supply unit for Zebra Printers used with the device can potentially overheat or cause a fire hazard.
FDA · DeviceRemel, IncDomestic distribution to AL, AZ, CA, FL, GA, IN, KS, KY, MD, MI, NE, NY, OH,…Official notice → - US
MEDLINE INDUSTRIES, LP - Northfield recalls Medline procedure kits labeled as: 1) EYE PACK, Pack Number VAL038BSCLC
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldWorldwide - US Nationwide and the country of Canada.Official notice →