Fitbit Recalls Force Activity-Tracking Wristband Due to Skin Irritation Risk
Fitbit is recalling Force activity-tracking wristbands because the materials can cause skin irritation, rashes, or blistering. Consumers should contact Fitbit for a full refund.
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a risk-of-harm product where injury (skin irritation and blistering) has been reported, fitting the High severity criteria for products with reported harm but no fatalities or severe systemic injuries.
Plain-English summary
Fitbit Inc. is recalling approximately 1,000,000 Fitbit Force wireless activity-tracking wristbands in the United States and about 28,000 in Canada. The recall involves model numbers FB402BK, FB402BKS, FB402SL, and FB402SLS. These wristbands function as pedometers, sleep monitors, and watches, featuring a plastic body with a stainless steel casing and clasp.
The recall was issued because users can develop allergic reactions to the stainless steel casing, strap materials, or adhesives used in assembly. These reactions can result in redness, rashes, or blistering where the skin has been in contact with the tracker. Fitbit has received about 9,900 reports of skin irritation and about 250 reports of blistering.
The wristbands were sold at AT&T, Best Buy, Brookstone, Dick's Sporting Goods, Radio Shack, REI, Sports Authority, Target, and other stores nationwide, as well as online at Amazon.com and Fitbit.com, from October 2013 to February 2014 for about $130. Consumers should contact Fitbit for a full refund.
The recalled product
- Product
- Wireless activity-tracking wristband
- Affected units
- 1,000,000
Distribution
Distributed nationwide across the United States.
Related recalls
Same hazard · skin irritation
See all →- HighFDA Recalls Medical Kits with Contaminated Pericare Wipes
FDA (Devices) · 2026-10-07
- SevereFDA Recalls Medical Kits with Contaminated Pericare Wipes
FDA (Devices) · 2026-10-07
- HighRecall of Medical Convenience Kits with Contaminated Pericare Wipes
FDA (Devices) · 2026-10-07
- ModerateCardinal Health Recalls Urinary Catheter Trays with Contaminated Wipes
FDA (Devices) · 2026-09-09
- ModerateCardinal Health Recalls Urinary Catheter Trays with Contaminated Wipes
FDA (Devices) · 2026-09-09
Similar recalls
- High
- SevereFitbit Recalls Ionic Smartwatches Due to Burn Hazard
CPSC · 2022-03-02
- HighProvata Recalls Activity Trackers Due to Burn Hazard
CPSC · 2018-09-25
- HighSPRI Ultra Heavy Resistance Bands Recalled for Injury Hazard
CPSC · 2019-10-04
- HighTarget Recalls Men's Sweatshirts for Flammability Safety Violations
CPSC · 2002-11-19
- SevereFDA Recalls Walnut Wearable Smart Thermometer Due to Reported Skin Burns
FDA (Devices) · 2023-06-14