FDA Device Intelligence
HomeAnacom Medtek › Series 7 Anacom MedTek

Series 7 Anacom MedTek

Anacom Medtek · Model A1501-087.1L · UDI-DI 00812324016830

ILQ
10
510(k) clearances
714
Adverse events (22 deaths)
19
Recalls
45
Facilities

Description

A speaker to be used by a patient when lying in bed or resting in a chair. It is a device that contains a speaker and cable and a connector for connection to a radio, television, infotainment or other sound emitting device. It has an audio jack plug for headphones. The sound level is regulated by the user with an adjustable control.

Recalls

DateFirmReason
2026-07-08Tobii Dynavox LlcUnder 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.
2026-07-08Tobii Dynavox LlcUnder 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.
2023-02-24Tobii Dynavox LlcProblem maintaining the stable placement of the battery may come loose from the housing and become damaged.
2022-05-31Baxter Healthcare CorporationAn issue has been identified with Phillips (Emergin) and Longleaf non relay (Connexall, Vocera, Cerner) wireless integrations used with NaviCare/Voalte Nurse Call, software version
2022-04-13Baxter Healthcare CorporationFirm discovered a firmware memory leak with a supplier-manufactured component.
2022-04-13Baxter Healthcare CorporationFirm discovered a firmware memory leak with a supplier-manufactured component.
2022-03-28Medminder Systems, Inc.Discontinuation of the Emergency Alert watch or pendant will no longer connect to the emergency alert system for all models. Older Model (legacy) without screen medical alert feat
2021-10-14Hill-Rom Inc.An unrecoverable error may occur where a component will fail to complete the reboot cycle, become non-functional and must be replaced.
2021-10-11Forbes Rehab Services IncWarning Added: Using damaged cables or chargers, or charging when moisture is present, can cause fire, electric shock, injury, or damage to Speech Generating Device or other proper
2017-12-14Dynavox Systems LlcThe battery is integral to the device. If the device sits unused and is not charged for a lengthy period of time (a few months) the battery will go into a deep discharge state and

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.