Severity
Moderate
ModerateActive
CPSC recall · Reported March 12, 2014
Fitbit Recalls Force Activity-Tracking Wristband Due to Risk of Skin Irritation
Users can develop allergic reactions to the stainless steel casing, materials used in the strap, or adhesives used to assemble the product, resulting in redness, rashes or blister…
Flextronics Sales & Marketing Ap Ltd., of Port Louis, Mauritius recalled This recall involves Fitbit Force™ wireless activity-tracking wristbands with model numbe… — a moderate-severity action.
Fitbit Recalls Force Activity-Tracking Wristband Due to Risk of Skin Irritation was recalled by Flextronics Sales & Marketing Ap Ltd., of Port Louis, Mauritius in March 12, 2014. Reason: Users can develop allergic reactions to the stainless steel casing, materials used in the strap, or adhesives…. Remedy: Consumers should contact Fitbit for a full refund.. Verify recall #14129 with the CPSC before acting.
The recall
Flextronics Sales & Marketing Ap Ltd., of Port Louis, Mauritius issued this moderate-severity CPSC recall — Users can develop allergic reactions to the stainless steel casing, materials used in the strap, or adhesives….
- Moderate
- severity level
- March 12, 2014
- reported
Sourced from official CPSC enforcement records. Verify recall #14129 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #14129) was formally reported on March 12, 2014. It is classified under Moderate severity, with a current status of Active. Flextronics Sales & Marketing Ap Ltd., of Port Louis, Mauritius is listed as the recalling firm. Federal records list the affected scope as About 1,000,000 in the U.S. and about 28,000 in Canada.
The documented reason for this recall is: Users can develop allergic reactions to the stainless steel casing, materials used in the strap, or adhesives used to assemble the product, resulting in redness, rashes or blistering where the skin has been in contact w… 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 contact Fitbit for a full refund. — 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 1,000,000 in the U.S. and about 28,000 in Canada
Related Recalls
6
0 from same agency
Product description
This recall involves Fitbit Force™ wireless activity-tracking wristbands with model numbers FB402BK, FB402BKS, FB402SL and FB402SLS. The wristband operates as a pedometer, sleep monitor and watch. It is made of plastic with a stainless steel casing and clasp and a small LED display screen. The display screen is flush with the top side of the band and a control button is on one side of the band. The wristband is about 3/4 inch wide and comes in large and small sizes and in the colors black or slate. The model number is on the back of the recalled wristband below the charging port.
Reason for recall
Users can develop allergic reactions to the stainless steel casing, materials used in the strap, or adhesives used to assemble the product, resulting in redness, rashes or blistering where the skin has been in contact with the tracker.
Remedy — what to do
Consumers should contact Fitbit for a full refund.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 14129 |
| Date reported | March 12, 2014 |
| Date initiated | March 12, 2014 |
| Recalling firm | Flextronics Sales & Marketing Ap Ltd., of Port Louis, Mauritius |
| Affected scope | About 1,000,000 in the U.S. and about 28,000 in Canada |
| 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 contact Fitbit for a full refund.
- Check the recall number (14129) 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 Fitbit Force™ wireless activity-tracking wristbands with model numbers FB402BK, FB402BKS, FB402SL and FB402SLS. The wristband operates as a pedometer, sleep monitor and watch. It is made of plastic with a stainless steel casing and clasp and a small LED display screen. The display screen is flush with the top side of the band and a control button is on one side of the band. The wristband is about 3/4 inch wide and comes in large and small sizes and in the colors black or slate. The model number is on the back of the recalled wristband below the charging port.. Recalled by Flextronics Sales & Marketing Ap Ltd., of Port Louis, Mauritius. Units affected: About 1,000,000 in the U.S. and about 28,000 in Canada.
Why was this product recalled? ▼
Users can develop allergic reactions to the stainless steel casing, materials used in the strap, or adhesives used to assemble the product, resulting in redness, rashes or blistering where the skin has been in contact with the tracker.
What should consumers do? ▼
Consumers should contact Fitbit for a full refund.
Which agency issued this recall? ▼
This recall was issued by the CPSC on March 12, 2014. Severity: Moderate. Recall number: 14129.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (14129) 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 March 12, 2014.
- 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.