Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported February 5, 2020
Cyberonics VNS Therapy AspireHC Model 105 Generator, 26-0007-4000/3. The firm name on the label is CYBERONICS, INC., Houston, TX. Vagus nerve stimulator.
This recall is an expansion of Z-3019-2017 and Z-3020-2017, which was initiated to fix the devices premature battery depletion, caused by electrical leakage on the circuit board a…
LivaNova USA Inc recalled Cyberonics VNS Therapy AspireHC Model 105 Generator, 26-0007-4000/3. The firm name on t… — a moderate-severity action.
Cyberonics VNS Therapy AspireHC Model 105 Generator, 26-0007-4000/3. The firm name on t… was recalled by LivaNova USA Inc in February 5, 2020. Reason: This recall is an expansion of Z-3019-2017 and Z-3020-2017, which was initiated to fix the devices premature …. Check the official notice for the remedy. Verify recall #Z-0868-2020 with the FDA Devices before acting.
The recall
LivaNova USA Inc issued this moderate-severity FDA Devices recall — This recall is an expansion of Z-3019-2017 and Z-3020-2017, which was initiated to fix the devices premature ….
- Moderate
- severity level
- 106 units
- affected scope
- Class II
- classification
- February 5, 2020
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0868-2020 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0868-2020) was formally reported on February 5, 2020, with the manufacturer initiating the action on November 16, 2018. It is classified under Moderate severity (Class II), with a current status of Terminated. LivaNova USA Inc is listed as the recalling firm, operating out of Houston, TX. Federal records list the affected scope as 106 devices.
The documented reason for this recall is: This recall is an expansion of Z-3019-2017 and Z-3020-2017, which was initiated to fix the devices premature battery depletion, caused by electrical leakage on the circuit board assemblies of the Models 105 and 106 gene… Distribution data in the federal record shows the product reached: Distribution US nationwide, including Puerto Rico. There was no foreign/military/government consignees.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Devices — 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
106 devices
Related Recalls
6
6 from same agency
Product description
Cyberonics VNS Therapy AspireHC Model 105 Generator, 26-0007-4000/3. The firm name on the label is CYBERONICS, INC., Houston, TX. Vagus nerve stimulator.
Reason for recall
This recall is an expansion of Z-3019-2017 and Z-3020-2017, which was initiated to fix the devices premature battery depletion, caused by electrical leakage on the circuit board assemblies of the Models 105 and 106 generators. *Note this recall occurred in November 2018.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0868-2020 |
| Date reported | February 5, 2020 |
| Date initiated | November 16, 2018 |
| Recalling firm | LivaNova USA Inc |
| Firm location | Houston, TX |
| Affected scope | 106 devices |
| Distribution | Distribution US nationwide, including Puerto Rico. There was no foreign/military/government consignees. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-0868-2020) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting — recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices 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? ▼
Cyberonics VNS Therapy AspireHC Model 105 Generator, 26-0007-4000/3. The firm name on the label is CYBERONICS, INC., Houston, TX. Vagus nerve stimulator.. Recalled by LivaNova USA Inc. Units affected: 106 devices.
Why was this product recalled? ▼
This recall is an expansion of Z-3019-2017 and Z-3020-2017, which was initiated to fix the devices premature battery depletion, caused by electrical leakage on the circuit board assemblies of the Models 105 and 106 generators. *Note this recall occurred in November 2018.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 5, 2020. Severity: Moderate. Recall number: Z-0868-2020.
Where was the recalled product distributed? ▼
Distribution: Distribution US nationwide, including Puerto Rico. There was no foreign/military/government consignees..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0868-2020) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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What to do next
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Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.
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Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Devices, reported February 5, 2020.
- 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.