Severity
Moderate
ModerateActive
CPSC recall · Reported June 2, 2015
ORTOVOX Recalls Avalanche Transceiver Due to Loss of Emergency Communications Capability
The S1+ hardware can fail, resulting in an inability to transmit a discoverable signal during an emergency situation, even as the unit appears to be powered on and functioning pro…
Ortovox, of Taufkirchen, Germany recalled The ORTOVOX S1+ transceiver is used as a beacon to locate an individual in the event of a… — a moderate-severity action.
ORTOVOX Recalls Avalanche Transceiver Due to Loss of Emergency Communications Capability was recalled by Ortovox, of Taufkirchen, Germany in June 2, 2015. Reason: The S1+ hardware can fail, resulting in an inability to transmit a discoverable signal during an emergency si…. Remedy: Consumers should stop using the recalled S1+ transceiver beacons immediately and return t…. Verify recall #15154 with the CPSC before acting.
The recall
Ortovox, of Taufkirchen, Germany issued this moderate-severity CPSC recall — The S1+ hardware can fail, resulting in an inability to transmit a discoverable signal during an emergency si….
- Moderate
- severity level
- June 2, 2015
- reported
Sourced from official CPSC enforcement records. Verify recall #15154 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #15154) was formally reported on June 2, 2015. It is classified under Moderate severity, with a current status of Active. Ortovox, of Taufkirchen, Germany is listed as the recalling firm. Federal records list the affected scope as About 3,000.
The documented reason for this recall is: The S1+ hardware can fail, resulting in an inability to transmit a discoverable signal during an emergency situation, even as the unit appears to be powered on and functioning properly. 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 stop using the recalled S1+ transceiver beacons immediately and return them to ORTOVOX for a free repair. — 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 — 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 — 40,409 medical devices recalls on record
Where this recall sits in the database
Of 100,165 recalls in the database, 23,668 are high severity, 72,097 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 3,000
Related Recalls
6
0 from same agency
Product description
The ORTOVOX S1+ transceiver is used as a beacon to locate an individual in the event of avalanche burial. The flip-case design transceiver is black with green accent stripes on the top sides. ORTOVOX and S1+ are printed on the top of the device. In the open/receive position the top half of the transceiver displays a blue screen with green border that displays an image and distance reading of the buried individual. The transceivers measure about 5 inches long by 3 inches wide by 1 inch thick in the closed/transmit position. All transceivers manufactured from 2010 through 2014 are included in the recall. The manufacture date is printed inside the battery door on the back of the transceiver with a roman numeral representing the quarter of the year and a two digit number referring to the year.
Reason for recall
The S1+ hardware can fail, resulting in an inability to transmit a discoverable signal during an emergency situation, even as the unit appears to be powered on and functioning properly.
Remedy — what to do
Consumers should stop using the recalled S1+ transceiver beacons immediately and return them to ORTOVOX for a free repair.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 15154 |
| Date reported | June 2, 2015 |
| Date initiated | June 2, 2015 |
| Recalling firm | Ortovox, of Taufkirchen, Germany |
| Affected scope | About 3,000 |
| 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 stop using the recalled S1+ transceiver beacons immediately and return them to ORTOVOX for a free repair.
- Check the recall number (15154) 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? ▼
The ORTOVOX S1+ transceiver is used as a beacon to locate an individual in the event of avalanche burial. The flip-case design transceiver is black with green accent stripes on the top sides. ORTOVOX and S1+ are printed on the top of the device. In the open/receive position the top half of the transceiver displays a blue screen with green border that displays an image and distance reading of the buried individual. The transceivers measure about 5 inches long by 3 inches wide by 1 inch thick in the closed/transmit position. All transceivers manufactured from 2010 through 2014 are included in the recall. The manufacture date is printed inside the battery door on the back of the transceiver with a roman numeral representing the quarter of the year and a two digit number referring to the year.. Recalled by Ortovox, of Taufkirchen, Germany. Units affected: About 3,000.
Why was this product recalled? ▼
The S1+ hardware can fail, resulting in an inability to transmit a discoverable signal during an emergency situation, even as the unit appears to be powered on and functioning properly.
What should consumers do? ▼
Consumers should stop using the recalled S1+ transceiver beacons immediately and return them to ORTOVOX for a free repair.
Which agency issued this recall? ▼
This recall was issued by the CPSC on June 2, 2015. Severity: Moderate. Recall number: 15154.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (15154) 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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What to do next
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Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: CPSC, reported June 2, 2015.
- Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records — no number is typed in by an editor. 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 June 2026.