Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported February 13, 2013
P10 Tobii battery box (product number 510410) Product Usage - Battery pack for MyTobii P10 Device. MyTobii P10 is a portable eye-controlled communication device featuring the Tobii Eye Control system.
Tobii ATI customers P10 external battery pack, which contains sealed lead-acid batteries, malfunctioned while recharging and produced smoke with a chemical smell.
Tobii Assistive Technology, Inc. recalled P10 Tobii battery box (product number 510410) Product Usage - Battery pack for MyTobii… - a moderate-severity action.
P10 Tobii battery box (product number 510410) Product Usage - Battery pack for MyTobii… was recalled by Tobii Assistive Technology, Inc. in February 13, 2013. Reason: Tobii ATI customers P10 external battery pack, which contains sealed lead-acid batteries, malfunctioned while…. Check the official notice for the remedy. Verify recall #Z-0766-2013 with the FDA Devices before acting.
The recall
Tobii Assistive Technology, Inc. issued this moderate-severity FDA Devices recall-Tobii ATI customers P10 external battery pack, which contains sealed lead-acid batteries, malfunctioned while….
- Moderate
- severity level
- 483 units
- affected scope
- Class II
- classification
- February 13, 2013
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0766-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0766-2013) was formally reported on February 13, 2013, with the manufacturer initiating the action on January 14, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Tobii Assistive Technology, Inc. is listed as the recalling firm, operating out of Dedham, MA. Federal records list the affected scope as 483 units.
The documented reason for this recall is: Tobii ATI customers P10 external battery pack, which contains sealed lead-acid batteries, malfunctioned while recharging and produced smoke with a chemical smell. Distribution data in the federal record shows the product reached: US Nationwide Distribution. 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, 3 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 - 40,322 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
483 units
Related Recalls
6
3 from same agency
Product description
P10 Tobii battery box (product number 510410) Product Usage - Battery pack for MyTobii P10 Device. MyTobii P10 is a portable eye-controlled communication device featuring the Tobii Eye Control system.
Reason for recall
Tobii ATI customers P10 external battery pack, which contains sealed lead-acid batteries, malfunctioned while recharging and produced smoke with a chemical smell.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0766-2013 |
| Date reported | February 13, 2013 |
| Date initiated | January 14, 2013 |
| Recalling firm | Tobii Assistive Technology, Inc. |
| Firm location | Dedham, MA |
| Affected scope | 483 units |
| Distribution | US Nationwide Distribution |
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-0766-2013) 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? ▼
P10 Tobii battery box (product number 510410) Product Usage - Battery pack for MyTobii P10 Device. MyTobii P10 is a portable eye-controlled communication device featuring the Tobii Eye Control system.. Recalled by Tobii Assistive Technology, Inc.. Units affected: 483 units.
Why was this product recalled? ▼
Tobii ATI customers P10 external battery pack, which contains sealed lead-acid batteries, malfunctioned while recharging and produced smoke with a chemical smell.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 13, 2013. Severity: Moderate. Recall number: Z-0766-2013.
Where was the recalled product distributed? ▼
Distribution: US Nationwide Distribution.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0766-2013) 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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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: FDA Devices, reported February 13, 2013. 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.