Roche Diabetes Care, Inc. recalls RocheDiabetes Care Platform Software version 2.5.2 material number 08888353001. This is a web application software hosted on a server.…
Potential for patient data mismatch when using browser "back" button to navigate between patients when using the diabetes management software.
Read the official notice →- Date
- 2022-05-04
- Country
- United States
- Brand
- Roche Diabetes Care
- Product
- RocheDiabetes Care Platform Software version 2.5.2 material number 08888353001. This is a web application software hosted on a server.…
- Classification
- Class II
- Units
- US Nationwide Distribution: AK, AZ, CA, CO, DC, FL, GA, IL, IN, MN, NC, NJ,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Roche Diabetes Care recalls
- 2024-07-03
USRoche Diabetes Care, Inc. recalls Accu-Chek Guide (SC) Kit -Intended to quantitatively measure glucose in fresh capillary whole blood from the fingertip, palm, and upper…
The reason for recall is the meters may show an incorrect measurement unit (mmol/L rather than mg/dL) and may result in the wrong unit of measure. Which may subsequently cause an error in interpreting a result as…
Other drugs & medical recalls in the United States
- 2022-05-04
- US
Draegar Medical Systems, Inc. recalls Drager Infinity CentralStation Software versions VG2.1.2 and VG2.1.2 SU12. For patient monitoring with Infinity M300 wireless…
Software issue resulting in temporary loss of central monitoring functionality.
FDA · DeviceDraegar Medical Systems, Inc.Worldwide distribution - US Nationwide distribution in the states of AL, AR,…Official notice → - US
Stryker GmbH recalls Smart Toe II Intramedullary Arthrodesis Implant
The nickel-sensitivity statement on the outer carton may be partially covered by a label resulting in the statement showing "Indicated for patients with Nickel sensitivity" instead of "Not Indicated for patients with…
FDA · DeviceStryker GmbHWorldwide distribution - US Nationwide and the countries including Australia,…Official notice → - US
Siemens Medical Solutions USA, Inc. recalls Acuson 9vE4 Transducer, Model (240)11289564 CE0129, Rx Only ,
Transducers (component of ultrasound system) may exceed recommended thermal index limits
FDA · DeviceSiemens Medical Solutions USA, Inc.Worldwide distribution - US Nationwide distribution in the states of…Official notice → - US
Carl Zeiss Meditec AG recalls ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.
High friction of the slider can cause the device to stick, or not move as intended.
FDA · DeviceCarl Zeiss Meditec AGU.S.: AL, AR, AZ, CA, CT, FL, GA, IA, IL, KS, LA, MA, MD, MI, MN, MO, MS, MT,…Official notice → - US
ROi CPS LLC recalls Convenience kits containing regard IV Start Kits: (1) regard Clinical Packaging Solutions, Item Number: 830015013, LD00200M - Vag Delivery…
A drug kit component was recalled by its manufacturer due to the potential for inadequacy of the validation of test methods used in its manufacture.
- US
Boston Scientific Corporation recalls SpaceOAR System, UPN SO-1010, SO-2101, SO-3101, and SO-4101. Used to temporarily position the anterior rectal wall away from the…
Users need to be aware that embolism is a possible adverse event associated with hydrogel misplacements. Updated IFU provides new procedural instructions, warnings and precautions that describe steps to verify correct…