Tobii Dynavox Llc recalls TD Navio Midi Speech Generating Device Model/Catalog Number: 1000798
Under certain conditions, the battery mounting tabs may become damaged, allowing the battery to move within the device enclosure, potentially leading to an internal short circuit. This may cause localized heating and…
Read the official notice →- Date
- 2026-08-26
- Country
- United States
- Brand
- Tobii Dynavox
- Product
- TD Navio Midi Speech Generating Device Model/Catalog Number: 1000798
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Tobii Dynavox recalls
- 2023-04-26
US
Tobii Dynavox Llc recalls Tobii Dynavox TD I-110 Speech Device-tablet style speech generating device used for ambulatory people with disabilities. Catalog #: 750567
Problem maintaining the stable placement of the battery may come loose from the housing and become damaged.
FDA · DeviceTobii Dynavox LlcWorldwide distribution - US Nationwide and the countries of Argentina,…Official notice →
Other drugs & medical recalls in the United States
- 2026-08-26
US
AVID Medical, Inc. recalls Halyard LAVH PACK, Model/Catalog Number: USAR053-11 containing Clearify Visualization System (5303907).
The kit component was subjected to EO sterilization, contrary to the manufacturer recommendation, which may have led to the component leaking in a kit.
US
Maquet Critical Care AB recalls GETINGE Y SENSOR Module, SERVO-U, SERVO-N, Model Number 6693662; part of the SERVO-U/-N continuous ventilator system, for facility use.…
The module did not undergo electrical safety tests and functional tests during production.
FDA · DeviceMaquet Critical Care ABUS Nationwide distribution in the states of CA, GA, MN, NY.Official notice →US
Boston Scientific Corporation recalls OverStitch Suture Cinch, 1pk. Endoscopic tissue approximation device.
Device may fail to deploy the cinch implant and/or fail to cut the suture as intended.
FDA · DeviceBoston Scientific CorporationWorldwide distribution - US Nationwide and the countries of Austria,…Official notice →US
Arrowhead DE LLC recalls Arrow-LOK Implant, REF: 21-253519, 21-253522, 21-253525, 21-253528, 21-253530, 21-253533, 21-253535, 21-253540, 21-253545, 21-253550,…
Implant did not undergo required gamma radiation dose audit. A potential reduction in sterility assurance could lead to patient infection.
FDA · DeviceArrowhead DE LLCUS Nationwide distribution in the states of VT, FL, TN, NY, GA, TX, HI.Official notice →US
Kico Knee Innovation Company recalls Brand Name: Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2 Model/Catalog Number: IN-29200 Software…
Due to an internal sensor issue, image displayed with eyepiece may appear tilted relative to the eyepiece housing
FDA · DeviceKico Knee Innovation CompanyConsignee Consignee Number Region Device Quantity RFK MEDICAL CE102 RICHMOND…Official notice →US
Philips North America Llc recalls Cardiac Workstation 5000. Product Number: 860439.
Device will intermittently provide inaccurate data related to native heart rate.
FDA · DevicePhilips North America LlcWorldwide distribution - US Nationwide and the countries of Australia,…Official notice →