HemoCue AB recalls The HemoCue Glucose 201 Microcuvettes are designed for use with the HemoCue Glucose 201 (or DM) Analyzer with plasma conversion that…
Glucose microcuvettes experienced transit time outside of limits, so stability through the whole microcuvette lifetime can no longer be guaranteed. The affected products may not have been stored at the recommended…
Read the official notice →- Date
- 2025-07-09
- Country
- United States
- Brand
- HemoCue AB
- Product
- The HemoCue Glucose 201 Microcuvettes are designed for use with the HemoCue Glucose 201 (or DM) Analyzer with plasma conversion that…
- Classification
- Class II
- Units
- US Nationwide distribution in the state of AR.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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.
Other drugs & medical recalls in the United States
- 2025-07-09
USC.R. Bard Inc recalls REF: 123400,Bard Urologist's Tray, For the Obstructed Urethra
Cather packaging may contain the incorrect French size.
FDA · DeviceC.R. Bard IncWorldwide - US Nationwide distribution including in the states of AL, AR, AZ,…Official notice →- US
Ortho-Clinical Diagnostics, Inc. recalls VITROS Chemistry Products OP Reagent Gen 15. Model Number: 680 1997. The VITROS OP Reagent is a dual-chambered package…
Lots from Generation (GEN) 15 of VITROS Chemistry Products OP Reagent may generate lower than expected quality control (QC) results. If the customer is unable to get passing quality control results, then the customer…
FDA · DeviceOrtho-Clinical Diagnostics, Inc.Worldwide distribution - US Nationwide and the countries of Australia,…Official notice → - US
CHANGE HEALTHCARE CANADA COMPANY recalls Change Healthcare Cardiology Hemodynamics Software
Due to complaints, software update may cause software to unexpectedly shutdown.
FDA · DeviceCHANGE HEALTHCARE CANADA COMPANYWorldwide - US Nationwide distribution in the states of AL, AR, CA, FL, KY MO,…Official notice → - US
CORIN MEDICAL, LTD. recalls Apex Knee System. Model Numbers: KC-50090, KC-50097, KC-50110, KC-50117, KC-50130, KC-50135, KC-50137, KC-50150, KC-50155, KC-50157,…
Investigation has identified that the age of the nylon packaging material has caused a loss of integrity of some pouches.
FDA · DeviceCORIN MEDICAL, LTD.US Nationwide distribution in the states of CA, CO, FL, IL, OK, TX, UT.Official notice → - US
Philips Ultrasound, Inc recalls Philips eL18-4 EMT Transducer.
Ultrasound transducer devices were refurbished beyond their useful life.
FDA · DevicePhilips Ultrasound, IncDomestic: Nationwide Distribution; Foreign: Australia, Austria, Belgium,…Official notice → - US
LUMITHERA INC recalls Brand Name: Valeda Light Delivery System Product Name: Light Based Device for Dry Age Related Macular Degeneration Product Description:…
U.S. customers were shipped devices that were configured for the European Union and were unable to plug the device in the electrical outlet.
FDA · DeviceLUMITHERA INCUS Nationwide distribution in the states of AZ, CA, FL, IL, ND, TN, TX.Official notice →