Drugs & medicalClass II

Fujifilm Irvine Scientific, Inc. recalls Sperm separation media are used to separate motile sperm from other constituents of semen.

The lower layer component of a sperm separation Kit does not match the certificate of analysis. The kit should contain lower layer (Lot: 0000020686, Shelf Life: 31 December 2024) but incorrectly may contain lower layer…

Read the official notice →
Date
2024-02-14
Country
United States
Brand
Fujifilm Irvine Scientific
Product
Sperm separation media are used to separate motile sperm from other constituents of semen.
Classification
Class II
Units
US: OK, CA, DC, NC, NV, TX, MI, IN, NY, UT, WI, MN, PA, WV, NJ, IL, LA, WA,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. 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 Fujifilm Irvine Scientific recalls

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    FDA · DeviceFujifilm Irvine Scientific, Inc.U.S.: AZ, AR, CA, CT, DC, FL, HI, IA, ID, IL, IN, KS, MA, MD, ME, MI, MN, MO,…Official notice →
  3. 2021-11-24
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    Fujifilm Irvine Scientific, Inc. recalls Vit Kit-Freeze is intended for use in assisted reproductive procedures for vitrification and storage of human oocytes (MII),…

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All 3 Fujifilm Irvine Scientific recalls →

Other drugs & medical recalls in the United States

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    The expiration date is missing from the primary (inner) packaging. The secondary (outer) box label correctly states the expiration date of February 12, 2033, for this lot

    FDA · DeviceOlympus Corporation of the AmericasWorldwide distribution - US Nationwide and the countries of Australia.Official notice →
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    Potential for a negative bias with quality control (QC) and patient sample results when using the Atellica CH Immunoglobulin M_2 (IgM_2) reagent.

    FDA · DeviceSiemens Healthcare Diagnostics, Inc.Worldwide - US Nationwide distribution including in the states of AL, AR, AZ,…Official notice →
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    Howmedica Osteonics Corp. recalls HRIS ACET CUP CUT TIP 26X140 Part Number: 6210-5-100. single-use, sterile surgical instruments used during hip arthroplasty

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    FDA · DeviceHowmedica Osteonics Corp.Worldwide distribution - US Nationwide and the countries of Argentina,…Official notice →
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    Globus Medical, Inc. recalls Globus Medical Cranial Drill, 6.00mm - instruments for access, preparation, and placement of cranial devices with the ExcelsiusGPS. Ref:…

    Sterile-packed Cranial Drills may not be sterile due to a breach in the packaging and/or may have discoloration near the drill tip.

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    BioFire Diagnostics, LLC recalls FilmArray Pneumonia Panel Plus (Pneumoplus), REF: RFIT-ASY-0143, CED 2797, IVD, Rx Only (30 test kit)

    Their is a potential for false positive results when using Pneumonia panel.

    FDA · DeviceBioFire Diagnostics, LLCWorldwide - US Nationwide distribution including in the states of AL, AR, AZ,…Official notice →
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    Randox Laboratories Ltd. recalls RX Series Copper (Cu) Assay Ref. Number CU2340

    Randox Laboratories have released an update to the Carryover Avoidance Technical Bulletin to detail that Copper, should not be run directly after Total Protein, on the RX series instruments testing order. If copper…

    FDA · DeviceRandox Laboratories Ltd.US Nationwide distribution in the states of SC and OK.Official notice →
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