CPSC recall · Reported December 17, 2009
CO2 Bicycle Tire Inflators Sold at Walmart Recalled by Todson Inc. Due to Risk of Injury
The pressurized cartridge containing carbon dioxide (CO2) can forcefully separate from the pump head, posing a risk of injury to the consumer.
The CPSC recalled This recall involves Zefal CO2 bicycle tire inflators with a small pressurized carbon dio….
CO2 Bicycle Tire Inflators Sold at Walmart Recalled by Todson Inc. Due to Risk of Injury was recalled and listed by the CPSC in December 17, 2009. Reason: The pressurized cartridge containing carbon dioxide (CO2) can forcefully separate from the pump head, posing …. Remedy: Consumers should immediately stop using the inflators and return them to Walmart for a fu…. Verify recall #10081 with the CPSC before acting.
The recall
issued this CPSC recall-The pressurized cartridge containing carbon dioxide (CO2) can forcefully separate from the pump head, posing ….
- None
- agency class
- December 17, 2009
- reported
Sourced from official CPSC enforcement records. Verify recall #10081 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. Consumers holding this product should act on the agency's documented remedy above 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 - 41,021 medical devices recalls on record
Product description
This recall involves Zefal CO2 bicycle tire inflators with a small pressurized carbon dioxide cartridge. The metal cartridge is threaded into the inflator head, which allows for the controlled release of carbon dioxide into the bicycle inner tube. The recalled inflators have "Zefal EZ+ CO2 inflator" printed on the front of the package. Model number 5602 and UPC number 798661556020 is printed on the back.
Reason for recall
The pressurized cartridge containing carbon dioxide (CO2) can forcefully separate from the pump head, posing a risk of injury to the consumer.
Remedy, what to do
Consumers should immediately stop using the inflators and return them to Walmart for a full refund.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Not classified by agency |
| Status | Active |
| Recall number | 10081 |
| Date reported | December 17, 2009 |
| Date initiated | December 17, 2009 |
| Recalling firm | Not disclosed |
| Affected scope | About 24,000 |
| 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 immediately stop using the inflators and return them to Walmart for a full refund.
- Check the recall number (10081) 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? ▼
Why was this product recalled? ▼
What should consumers do? ▼
Which agency issued this recall? ▼
How do I report an injury from a recalled product? ▼
Nationwide recalls with similar severity or category timing
Consumer-product notices outside this firm and state, matched by severity timing and product category.
Similar severity · nearest report date
Same archive severity grade, closest by report date among other firms and states.
Similar Medical Devices · nearest report date
Same product category, closest by report date among other firms and states (deduped against the severity set).
Compare this recall with GORE VIABIL Short Wire Biliary Endoprosthesis, Model No. VS… → · All Medical Devices recalls
Methodology · Corrections · Archive as of August 2026