Abbott Diagnostics Scarborough, Inc. recalls Brand Name: ID NOW Influenza A/B 2 24T Product Name: ID NOW Influenza A/B 2 24T Model/Catalog Number: 427-000 Software…
the impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.
Read the official notice →- Date
- 2025-04-23
- Country
- United States
- Brand
- Abbott Diagnostics Scarborough
- Product
- Brand Name: ID NOW Influenza A/B 2 24T Product Name: ID NOW Influenza A/B 2 24T Model/Catalog Number: 427-000 Software Version: N/A…
- Classification
- Class II
- Units
- US Nationwide distribution.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Abbott Diagnostics Scarborough recalls
- 2026-03-25
USAbbott Diagnostics Scarborough, Inc. recalls Product Name: ID NOW" Influenza A & B 2 Model/Catalog Number: 427-000 Software Version: Not Applicable Product Description:…
It was confirmed that the impacted lot has a higher occurrence of invalid rates when compared to the product Instructions for Use.
- 2025-04-23
- US
Abbott Diagnostics Scarborough, Inc. recalls Brand Name: ID NOW Influenza A/B 2 24T Product Name: ID NOW Influenza A/B 2 24T Model/Catalog Number: 427-000 Software…
The impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.
FDA · DeviceAbbott Diagnostics Scarborough, Inc.Worldwide distribution - US Nationwide and the countries of Australia;…Official notice →
Other drugs & medical recalls in the United States
- 2025-04-23
- US
Channel Medsystems, Inc. recalls Brand Name: Cerene Cryotherapy Device Product Name: DEVICE, THERMAL ABLATION, ENDOMETRIAL Model/Catalog Number: FGS-7000 Product…
Due to evaporator gasket not sealing which can cause liquid nitrous oxide to drip/leak from the bottom of the device handle during treatment or after treatment during venting of the device
FDA · DeviceChannel Medsystems, Inc.U.S Nationwide distribution in the states of AL, AZ, CA, CO, CT, DE, FL, GA,…Official notice → - US
Micro-X Ltd. recalls Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number: MXU-RV35 Product Description: Rover Mobile X-rays System…
Potential for early life x-ray tube failure for mobile x-ray system due to excessive thermal load on the anode.
FDA · DeviceMicro-X Ltd.US Nationwide distribution in the states of CA, NJ, and Puerto Rico (US…Official notice → - US
Maquet Cardiovascular, LLC recalls Maquet VH-3010 Power Supply. Used to deliver power to the harvesting tool of the Vasoview Hemopro EVH System (HemoPro 2).
Incorrect resistor utilized in the VH-3010 Power Supply, which may cause the jaws of the HemoPro 2 to not adequately heat up.
FDA · DeviceMaquet Cardiovascular, LLCWorldwide - US Nationwide distribution in the states of AL, CA, CO, DC, FL,…Official notice → - US
Abbott Diagnostics Scarborough, Inc. recalls Brand Name: ID NOW Influenza A/B 2 24T Product Name: ID NOW Influenza A/B 2 24T Model/Catalog Number: 427-000 Software…
The impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.
FDA · DeviceAbbott Diagnostics Scarborough, Inc.Worldwide distribution - US Nationwide and the countries of Australia;…Official notice → - US
Thoratec LLC recalls HeartMate Mobile Power Unit: REF: 107754, NA; 107758, EU; 107758AU, AU; 107758UK, UK; L107758, EU Rental. Used with HeartMate 3 and II…
Left Ventricular Assist System Mobile Power Unit (MPU) may have electrical component that may cause MPU not to turn on, unprompted shut down, or turning off/restarting, may cause system controller to indicate Yellow…
FDA · DeviceThoratec LLCWorldwide - US Nationwide distribution in the states of WA, NE, VA, PA, DC,…Official notice → - US
Conformis Inc. recalls restor3d Cordera Hip System. ACETABULAR LINER GRP C 36MM LIP. Model Number: HDL-060-C22L-000101 Acetabular Liner for Cordera Hip System
The hip cup liner that was packaged with the incorrect labeling. HDL-060-C22S-000101 from Lot 1788258 contained a hooded liner, but it was labeled to have a standard liner.
FDA · DeviceConformis Inc.US Nationwide distribution in the states of CA, FL, NV, TN.Official notice →