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 (…
Read the official notice →- Date
- 2025-09-10
- Country
- United States
- Brand
- Merge Healthcare
- Product
- Merge Hemo, Model RCSV2, Model/Catalog Number 99-01172-00, software versions 11.1 and 11.1.1 Product Description: The Merge Hemo, Model…
- Classification
- Class II
- Units
- US Nationwide distribution including in the states of Arizona, Arkansas,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 → - 2025-03-26
- US
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…
Other drugs & medical recalls in the United States
- 2025-09-10
- US
CARIS LIFE SCIENCES recalls MI Cancer Seek REF MSC000 UDI Code: (01)00860008613325(21)H5HJHDSXF MI Cancer Seek is a single-site assay intended to provide tumor…
Due to an incorrect test results provided that indicated the incorrect drug therapy recommendation
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O&M HALYARD INC recalls Orthopedic Pack, Model: 88041-12 AC2424601B 09/02/2029 Universal Pack, Model: 77165-06 AC2424902B 09/05/2029
Surgical drape packs may have open seals, which may compromise the sterility of the product.
FDA · DeviceO&M HALYARD INCWorldwide - US Nationwide distribution in the states of GA, AL, PA and the…Official notice → - US
Lumicell, Inc. recalls Brand Name: 900-00218 Sterile Cover 10-Pack Shipper Box Assembly Product Name: 900-00218 Sterile Cover 10-Pack Shipper Box Assembly…
The potential of the elastic bands included in the kit detaching or fracturing during surgical procedures. As a result, these failures may pose a risk of retained foreign bodies in the surgical cavity and potentially…
FDA · DeviceLumicell, Inc.US Nationwide distribution in the states of CA, FL, MA, NC, TX.Official notice → - US
Flosonics Medical (R/A 1929803 ONTARIO CORP.) recalls FloPatch FP120, REF: FP120-FOT01-005
Flowmeter patch as a human readable expiry date on the outer shipping packaging that reads 2025-06-20 when it should read 2026-06-20.
FDA · DeviceFlosonics Medical (R/A 1929803 ONTARIO CORP.)US Nationwide distribution in the state of California.Official notice → - US
PREMIA SPINE LTD recalls TOPS Inserter, part of the TOPS System Instrument Set used for implantation of the TOPS System. Model Number: 82889.
Potential for missing pins at tip of inserter.
FDA · DevicePREMIA SPINE LTDUS Nationwide distribution in the state of Connecticut.Official notice → - US
Bio-Rad Laboratories, Inc. recalls Platelia Toxo IgM Catalog Number 26211 UDI Code: 03610520005552 The Platelia Toxo IgM assay is a semi-quantitative immunocapture…
Due to a risk of false positive results that could lead to unnecessary medical treatment.
FDA · DeviceBio-Rad Laboratories, Inc.U.S. Nationwide distribution in the states of CA, CO, FL, NC and NV.Official notice →