Agilent Technologies, Inc. recalls Kit Label: Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF K589911-2 Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF…
Label provided for substrate vail contained incorrect expiration date.
Read the official notice →- Date
- 2022-07-20
- Country
- United States
- Brand
- Agilent Technologies
- Product
- Kit Label: Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF K589911-2 Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF…
- Classification
- Class III
- Units
- U.S. Nationwide distribution in the states of NY and VA.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Agilent Technologies recalls
- 2025-04-16
USAgilent Technologies, Inc. recalls GenetiSure Dx Labeling Kit, REF: K1201-64105, contains human reference DNA female aliquot, REF5190-7317. A required kit for the…
DNA Labeling Kit for use in sample labeling to be hybridized to oligonucleotide microarrays has a component, Human Reference DNA Female aliquot, affected by a mosaic aberration that may result in Chromosome 12 baseline…
FDA · DeviceAgilent Technologies, Inc.US distribution to the state of: MA and OUS (International) distribution to…Official notice →- 2024-06-05
- US
Agilent Technologies recalls Brand Name: Dako CoverStainer, Dako CoverStainer CPO Product Name: CoverStainer, CoverStainer CPO Model/Catalog Number: CS10030, CS10040,…
There is the potential for the front plexiglass door of the automated slide processing system to break causing potential injury.
FDA · DeviceAgilent TechnologiesWorldwide - US Nationwide distribution in the states of CA, TN, MI, MD, MA,…Official notice →
Other drugs & medical recalls in the United States
- 2022-07-27
- US
- US
Vi-Jon, LLC recalls Hydrogen Peroxide Topical Solution USP, 3%, 16 FL OZ (1 PT) 473 mL bottle, packaged as a) Signature Care NDC 21130-871-43 UPC 3…
Cross Contamination With Other Products: Product is cross contaminated with low levels of isopropyl alcohol.
- 2022-07-20
- US
Hamilton Medical AG recalls HAMILTON-H900 Humidifier, Models: 950001, 950004
When starting a humidifier, intended for respiratory gas conditioning during invasive and noninvasive mechanical ventilation, with an empty chamber, and water is not filled into the chamber, the low water level alarm…
- US
Aesculap Implant Systems LLC recalls AESCULAP TC COOELY MICRO NEEDLEHLDER SERR 200MM, product code MG524R. manual surgical instrument designed to grasp a suture needle
Needleholder incorrectly labeled as 200MM when the actual instrument size is 150MM.
- US
Breas Medical, Inc. recalls Vivo 45LS Ventilator- intended to provide continuous or intermittent ventilatory support for the care of individuals who require…
A forced shutdown of one of the processors did not generate a watch dog alarm, would develop into a failure AND the instructions to monitor a ventilator dependent patient are NOT followed, the health consequences could…
- US
Ivenix, Inc. recalls Ivenix Infusion System (IIS)
Downstream occlusion alarm is sometimes immediately followed by a pump problem alarm.