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CPSC recall · Reported January 30, 2014

Strollers Recalled by Britax Due to Partial Fingertip Amputation Hazard

The hinge on the stroller's folding mechanism can partially amputate consumers' fingertips, break their fingers or cause severe lacerations, among other injuries, when they press …

Recall #
14098
Affected scope
About 216,000 in the United States and 8,800 in Canada
Verify with CPSC →
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The CPSC recalled This recall involves Britax B-Agile, B-Agile Double and BOB Motion strollers. The single … — a moderate-severity action.

Strollers Recalled by Britax Due to Partial Fingertip Amputation Hazard was recalled and listed by the CPSC in January 30, 2014. Reason: The hinge on the stroller's folding mechanism can partially amputate consumers' fingertips, break their finge…. Remedy: Consumers should stop using the recalled strollers immediately and contact Britax to rece…. Verify recall #14098 with the CPSC before acting.

The recall

issued this moderate-severity CPSC recall — The hinge on the stroller's folding mechanism can partially amputate consumers' fingertips, break their finge….

Moderate
severity level
January 30, 2014
reported

Sourced from official CPSC enforcement records. Verify recall #14098 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This CPSC action (record #14098) was formally reported on January 30, 2014. It is classified under Moderate severity, with a current status of Active. The recalling firm is not specified in the federal record. Federal records list the affected scope as About 216,000 in the United States and 8,800 in Canada.

The documented reason for this recall is: The hinge on the stroller's folding mechanism can partially amputate consumers' fingertips, break their fingers or cause severe lacerations, among other injuries, when they press the release button while pulling on the … 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 strollers immediately and contact Britax to receive a free repair kit. — 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.

Children & Baby Products recalls over time

Where this recall sits in its category — 3,146 children & baby products recalls on record

0100200300400500 20052008201120142017202020232026 128

Where this recall sits in the database

Severity2366872097High severity (most serious)Moderate severityLow severity
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.

Severity

Moderate

Affected scope

About 216,000 in the United States and 8,800 in Canada

Related Recalls

6

0 from same agency

Product description

This recall involves Britax B-Agile, B-Agile Double and BOB Motion strollers. The single and double strollers were sold in various color schemes, including black, red, kiwi, sandstone, navy and orange. They were manufactured between March 2011 and June 2013 and have the following model numbers: U341763, U341764, U341782 and U341783 for the B-Agile strollers; U361818 or U361819 for the B-Agile Double strollers; and U391820, U391821 and U391822 for the BOB Motion strollers. The model number and the manufacture date in YYYY/MM/DD format can be found on label located on the inside of the stroller's metal frame near the right rear wheel.

Reason for recall

The hinge on the stroller's folding mechanism can partially amputate consumers' fingertips, break their fingers or cause severe lacerations, among other injuries, when they press the release button while pulling on the release strap.

Remedy — what to do

Consumers should stop using the recalled strollers immediately and contact Britax to receive a free repair kit.

Recall Profile

Structured summary of the CPSC recall record
Attribute Value
Agency U.S. Consumer Product Safety Commission
Severity class Moderate
Status Active
Recall number 14098
Date reported January 30, 2014
Date initiated January 30, 2014
Recalling firm Not disclosed
Affected scope About 216,000 in the United States and 8,800 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 stop using the recalled strollers immediately and contact Britax to receive a free repair kit.

  • Check the recall number (14098) 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 Britax B-Agile, B-Agile Double and BOB Motion strollers. The single and double strollers were sold in various color schemes, including black, red, kiwi, sandstone, navy and orange. They were manufactured between March 2011 and June 2013 and have the following model numbers: U341763, U341764, U341782 and U341783 for the B-Agile strollers; U361818 or U361819 for the B-Agile Double strollers; and U391820, U391821 and U391822 for the BOB Motion strollers. The model number and the manufacture date in YYYY/MM/DD format can be found on label located on the inside of the stroller's metal frame near the right rear wheel.. Units affected: About 216,000 in the United States and 8,800 in Canada.
Why was this product recalled?
The hinge on the stroller's folding mechanism can partially amputate consumers' fingertips, break their fingers or cause severe lacerations, among other injuries, when they press the release button while pulling on the release strap.
What should consumers do?
Consumers should stop using the recalled strollers immediately and contact Britax to receive a free repair kit.
Which agency issued this recall?
This recall was issued by the CPSC on January 30, 2014. Severity: Moderate. Recall number: 14098.
How do I check if my product is affected by a recall?
Check the product description and recall number (14098) 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.

Nearby Recalls in This Category

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: CPSC, reported January 30, 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.