Illumina, Inc. recalls illumina Model NextSeq 550 Dx REF 20005715
cybersecurity vulnerability
Read the official notice →- Date
- 2022-06-22
- Country
- United States
- Brand
- Illumina
- Product
- illumina Model NextSeq 550 Dx REF 20005715
- Classification
- Class II
- Units
- Worldwide distribution - U.S. Nationwide distribution including in the states…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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.
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- 2026-10-07
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Illumina, Inc. recalls Reagent Kits/ containing flow cells, components of NextSeq 550Dx Instrument: NextSeq 550Dx High Output Reagent Kit v2.5 (75 cycles) IVD,…
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FDA · DeviceIllumina, Inc.Worldwide - US Nationwide distribution in the states of PA, NJ, CA, NC, UT,…Official notice → - 2023-06-28
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FDA · DeviceIllumina, Inc.Worldwide distribution - US Nationwide and the countries of Algeria, AU…Official notice → - 2022-04-06
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Illumina, Inc. recalls Illumina NextSeq 550Dx, REF: 20005715, CE, IVD
There is a potential that the DNA sequence analyzer may short circuit shortly after disconnection and reconnection of circuit board or imaging module due to an insufficient reconnection of the ribbon cable. The short…
FDA · DeviceIllumina, Inc.US: PA, WA, CA, MI, FL, MD, AR, UT NC, Fl, IL, NE, NJ, TN, NY, IN, CO, GA, OK,…Official notice →
Other drugs & medical recalls in the United States
- 2022-06-22
- US
GE Healthcare, LLC recalls CARESCAPE Central Station (CSCS) V2, Model numbers 2082278-001 and 2082279-001. Update 3/10/2023: The following FRU and display part…
The CARESAPE Central Station (CSCS) V2 can shut down due to a potential power supply component failure. This can lead to loss of patient monitoring at the central station.
FDA · DeviceGE Healthcare, LLCWorldwide distribution - US Nationwide. There was also military/government…Official notice → - US
Olympus Corporation of the Americas recalls Olympus URETERO-RENO FIBERSCOPE Model: URF-P6R
Incorrect adhesive used to secure the diopter ring and nameplate ring. Improperly connected diopter ring may result in the loss of adjustment function leading to a blurred field of vision and unintentional contact with…
- US
Micro Therapeutics, Inc. recalls AXIUM DETACHABLE COIL SYSTEM REF QC-4-12-HELIX; Axium Detachable Coil System REF QC-10-30-3D;
Due to incorrect size and configuration labeling of the detachable coil system.
FDA · DeviceMicro Therapeutics, Inc.International distribution in the countries of China and Republic of Korea.Official notice → - US
Tandem Diabetes Care Inc recalls t:slim X2 Insulin Pump with Dexcom G5 Mobile CGM, and t:slim X2 Insulin Pump with Basal-IQ Technology
Insulin pumps may display unexpected fluctuation of the remaining battery life so ensure pump battery life does not fall below 25% remaining power. If the battery life drops to less than 5%, insulin delivery will…
FDA · DeviceTandem Diabetes Care IncInternational distribution in the country of Australia.Official notice → - US
Draeger Medical, Inc. recalls Drager SafeStar 55, Catalog No. MP01790
Possible occlusion of filters due to manufacturing error.
FDA · DeviceDraeger Medical, Inc.Worldwide distribution - US Nationwide distribution in the states of AZ, CA,…Official notice → - US
Walmart Inc recalls Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets, ORIGINAL, 100-count bottles, UPC 7 501031 12705.
Marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.