Fujifilm Irvine Scientific, Inc. recalls Vit Kit-Freeze is intended for use in assisted reproductive procedures for vitrification and storage of human oocytes (MII),…
Due to a component in kit being labeled with the incorrect Expiration Date
Read the official notice →- Date
- 2021-11-24
- Country
- United States
- Brand
- Fujifilm Irvine Scientific
- Product
- Vit Kit-Freeze is intended for use in assisted reproductive procedures for vitrification and storage of human oocytes (MII), pronuclear…
- Classification
- Class II
- Units
- Worldwide Distribution: U.S. (nationwide) to states of: AL, AK, AZ, CA, CT,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Fujifilm Irvine Scientific recalls
- 2024-02-14
USFujifilm 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…
FDA · DeviceFujifilm Irvine Scientific, Inc.US: OK, CA, DC, NC, NV, TX, MI, IN, NY, UT, WI, MN, PA, WV, NJ, IL, LA, WA,…Official notice →- 2023-04-05
- US
Fujifilm Irvine Scientific, Inc. recalls Irvine Scientific Oil for Embryo Culture (Light Mineral Oil) REF Catalog # 9305
Due to the detection of oil toxicity in several lots of Oil for Embryo Culture products.
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 →
Other drugs & medical recalls in the United States
- 2021-11-24
- US
CooperSurgical, Inc. recalls Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075-05W
XXX
FDA · DeviceCooperSurgical, Inc.US Nationwide Distribution Foreign: ARMENIA, BOLIVIA, CAMBODIA, CANADA, CHILE,…Official notice → - US
CooperSurgical, Inc. recalls Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075
Coagulate function may not operate with the use of the Hand Switch, failure of the device to coagulate tissue may lead to a prolonged procedure requiring medical intervention to control any intraoperative bleeding and…
FDA · DeviceCooperSurgical, Inc.US Nationwide Distribution Foreign: ARMENIA, BOLIVIA, CAMBODIA, CANADA, CHILE,…Official notice → - US
ROi CPS LLC recalls REGARD Vitrectomy Tray
Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of Specifications was used as a component in some of the ROI CPS, LLC products.
- US
Ortho-Clinical Diagnostics, Inc. recalls VITROS Immunodiagnostic Products Anti-HBc IgM Controls, Product Code 6801427 For use in monitoring the performance of the VITROS…
Ortho Clinical Diagnostics confirmed a complaint that some VITROS Immunodiagnostic Products Anti-HBc IgM Controls Lot 1690 Controls Values booklet contained information for the incorrect product. While the accuracy of…
FDA · DeviceOrtho-Clinical Diagnostics, Inc.US (Domestic) distribution to states of: AZ, CA, CO, CT, FL, GA, LA, MA, MO,…Official notice → - US
Medicalplastic S.R.L. recalls Ilizarov Wire Tensioner, Model 71070341, UDI (10)08033201842072(10)21HP02550(11)210831(21E434
Medicalplastic s.r.l. is conducting a voluntary field action to remove a group of Ilizarov Wire Tensioners due to a manufacturing error. An internal washer of the Ilizarov Wire Tensioner has been made in a wrong…
- US
Laboratoires Bodycad, Inc. recalls Torque Limiting Adaptor, AO Connect, 4 N-m, part #027-203, reusable, a component of the Bodycad Fine Osteotomy Implant and Disposable…
There is a risk of breakage of the torque limiting adaptor if used counterclockwise and it must not be used with a power tool due to no test data validating this use.
FDA · DeviceLaboratoires Bodycad, Inc.Distribution was made to CO, MI, and NY. Foreign distribution was made to…Official notice →