Severity
Moderate
ModerateActive
CPSC recall · Reported July 26, 2016
Inovonics Recalls Pendants, Universal Transmitters and Receivers Due to Alarm Failure (Recall Alert)
The transmitters and receivers can fail to send or receive a signal for help in an emergency.
Inovonics, of Louisville, Colo. recalled This recall involves Inovonics transmitters and receivers. These beige devices transmit o… - a moderate-severity action.
Inovonics Recalls Pendants, Universal Transmitters and Receivers Due to Alarm Failure (Re… was recalled by Inovonics, of Louisville, Colo. in July 26, 2016. Reason: The transmitters and receivers can fail to send or receive a signal for help in an emergency.. Remedy: Consumers should immediately stop using the recalled transmitters and receiver and contac…. Verify recall #16760 with the CPSC before acting.
The recall
Inovonics, of Louisville, Colo. issued this moderate-severity CPSC recall-The transmitters and receivers can fail to send or receive a signal for help in an emergency..
- Moderate
- severity level
- July 26, 2016
- reported
Sourced from official CPSC enforcement records. Verify recall #16760 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #16760) was formally reported on July 26, 2016. It is classified under Moderate severity, with a current status of Active. Inovonics, of Louisville, Colo. is listed as the recalling firm. Federal records list the affected scope as About 5,500.
The documented reason for this recall is: The transmitters and receivers can fail to send or receive a signal for help in an emergency. Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. The remedy documented by the agency is: Consumers should immediately stop using the recalled transmitters and receiver and contact Inovonics for a free replacement. All known purchasers have been notified directly by the firm. - consumers holding this product should act on that instruction rather than relying on general guidance.
Within the same product category the archive holds 6 closely related recalls, 3 from CPSC - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
About 5,500
Related Recalls
6
3 from same agency
Product description
This recall involves Inovonics transmitters and receivers. These beige devices transmit or receive signals for emergency call systems in senior independent and assisted living communities, as well as security monitoring systems in commercial buildings and some luxury residences. Recalled models include EN1210, EN1223S, EN1233S and EN4232MR. The EN1223S and EN1233S wireless pendant transmitters allow users to push a button to summon assistance. "Inovonics" is printed on all the devices except on model EN1223S. The model number appears on a label on the back of the device. The date code is printed on the carton label and on the circuit board inside the device. Model Number Placement Function Carton Date Code Date Codes on Printed Circuit Board Label Inside Device EN1210 Mounted on door/window frame Alarm sent if door or window is opened 16075 16074 16075 EN1223S Worn on neck, wrist or belt Allows user to push button to summon assistance 16075 16071 16083 16077 16080 16081 EN1233S Worn on neck or belt Allows user to push button to summon assistance 16073 16072 EN4232MR Mounted on wall Receives messages from Inovonics transmitters 16077 16075 16076
Reason for recall
The transmitters and receivers can fail to send or receive a signal for help in an emergency.
Remedy, what to do
Consumers should immediately stop using the recalled transmitters and receiver and contact Inovonics for a free replacement. All known purchasers have been notified directly by the firm.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 16760 |
| Date reported | July 26, 2016 |
| Date initiated | July 26, 2016 |
| Recalling firm | Inovonics, of Louisville, Colo. |
| Affected scope | About 5,500 |
| Distribution | Not disclosed |
| Official source | CPSC notice → |
Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.
What to do with this recall
Consumers should immediately stop using the recalled transmitters and receiver and contact Inovonics for a free replacement. All …
- Check the recall number (16760) and product description against the item you own. Search the archive
- Confirm the current status and remedy on the official CPSC notice before acting. CPSC notice
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official CPSC record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
This recall involves Inovonics transmitters and receivers. These beige devices transmit or receive signals for emergency call systems in senior independent and assisted living communities, as well as security monitoring systems in commercial buildings and some luxury residences. Recalled models include EN1210, EN1223S, EN1233S and EN4232MR. The EN1223S and EN1233S wireless pendant transmitters allow users to push a button to summon assistance. "Inovonics" is printed on all the devices except on model EN1223S. The model number appears on a label on the back of the device. The date code is printed on the carton label and on the circuit board inside the device. Model Number Placement Function Carton Date Code Date Codes on Printed Circuit Board Label Inside Device EN1210 Mounted on door/window frame Alarm sent if door or window is opened 16075 16074 16075 EN1223S Worn on neck, wrist or belt Allows user to push button to summon assistance 16075 16071 16083 16077 16080 16081 EN1233S Worn on neck or belt Allows user to push button to summon assistance 16073 16072 EN4232MR Mounted on wall Receives messages from Inovonics transmitters 16077 16075 16076. Recalled by Inovonics, of Louisville, Colo.. Units affected: About 5,500.
Why was this product recalled? ▼
The transmitters and receivers can fail to send or receive a signal for help in an emergency.
What should consumers do? ▼
Consumers should immediately stop using the recalled transmitters and receiver and contact Inovonics for a free replacement. All known purchasers have been notified directly by the firm.
Which agency issued this recall? ▼
This recall was issued by the CPSC on July 26, 2016. Severity: Moderate. Recall number: 16760.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (16760) against your product. Visit the official CPSC website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
How do I report an injury from a recalled product? ▼
Report injuries to the issuing agency: CPSC at SaferProducts.gov, NHTSA at nhtsa.gov/report-a-safety-problem, or FDA via MedWatch. Document the product (photos, model/serial numbers, purchase receipts) and seek medical attention. Injury reports help agencies track hazard patterns and may strengthen enforcement actions.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: CPSC, reported July 26, 2016. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.