Severity
Moderate
ModerateActive
CPSC recall · Reported November 23, 2004
CPSC, Fitness Quest Inc. Announce Recall to Repair Ab Lounge™ Exercise Products
When opening or folding up these exercise machines, consumers can catch their fingers in the hinges. This can result in lacerations, crushing, or amputation to fingertips. This do…
Compiled from official public sources by the editorial team.
Verify with CPSC →
Fitness Quest Inc., of Canton, Ohio recalled The recall includes the Ab Lounge™, Ab Lounge™ 2, and Ab Lounge™ Ultimate exercisers. The… - a moderate-severity action.
CPSC, Fitness Quest Inc. Announce Recall to Repair Ab Lounge™ Exercise Products was recalled by Fitness Quest Inc., of Canton, Ohio in November 23, 2004. Reason: When opening or folding up these exercise machines, consumers can catch their fingers in the hinges. This can…. Remedy: Firm no longer in business. Recall remedy no longer available. Discard the product. Do no…. Verify recall #05055 with the CPSC before acting.
The recall
Fitness Quest Inc., of Canton, Ohio issued this moderate-severity CPSC recall-When opening or folding up these exercise machines, consumers can catch their fingers in the hinges. This can….
- Moderate
- severity level
- November 23, 2004
- reported
Sourced from official CPSC enforcement records. Verify recall #05055 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #05055) was formally reported on November 23, 2004. It is classified under Moderate severity, with a current status of Active. Fitness Quest Inc., of Canton, Ohio is listed as the recalling firm. Federal records list the affected scope as About 460,000.
The documented reason for this recall is: When opening or folding up these exercise machines, consumers can catch their fingers in the hinges. This can result in lacerations, crushing, or amputation to fingertips. This does not occur while users are exercising. 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: Firm no longer in business. Recall remedy no longer available. Discard the product. Do not donate or resell. - 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, 6 from CPSC - 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.
Outdoor & Sports recalls over time
Where this recall sits in its category - 510 outdoor & sports 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
About 460,000
Related Recalls
6
6 from same agency
Product description
The recall includes the Ab Lounge™, Ab Lounge™ 2, and Ab Lounge™ Ultimate exercisers. The machines have the name "Ab Lounge" or "Ab Lounge 2" printed on the upper front fabric of the seat. The recall involves machines with the following serial numbers: Ab Lounge™ machines: ALX-000001 through ALX-037999, and all machines that start with serial numbers 03 44 through 04 36. Ab Lounge™ 2 machines: AL2X-000001 through AL2X-059060, and all machines that start with serial numbers 04 03 through 04 36. Ab Lounge™ Ultimate machines: all machines that start with serial numbers 04 28 through 04 34. The serial number is located on a label on the bottom of the front frame. Ab Lounge™ exercise products with straight brackets that do not fold are not part of this recall.
Reason for recall
When opening or folding up these exercise machines, consumers can catch their fingers in the hinges. This can result in lacerations, crushing, or amputation to fingertips. This does not occur while users are exercising.
Remedy, what to do
Firm no longer in business. Recall remedy no longer available. Discard the product. Do not donate or resell.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 05055 |
| Date reported | November 23, 2004 |
| Date initiated | November 23, 2004 |
| Recalling firm | Fitness Quest Inc., of Canton, Ohio |
| Affected scope | About 460,000 |
| 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
Firm no longer in business. Recall remedy no longer available. Discard the product. Do not donate or resell.
- Check the recall number (05055) 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? ▼
The recall includes the Ab Lounge™, Ab Lounge™ 2, and Ab Lounge™ Ultimate exercisers. The machines have the name "Ab Lounge" or "Ab Lounge 2" printed on the upper front fabric of the seat. The recall involves machines with the following serial numbers: Ab Lounge™ machines: ALX-000001 through ALX-037999, and all machines that start with serial numbers 03 44 through 04 36. Ab Lounge™ 2 machines: AL2X-000001 through AL2X-059060, and all machines that start with serial numbers 04 03 through 04 36. Ab Lounge™ Ultimate machines: all machines that start with serial numbers 04 28 through 04 34. The serial number is located on a label on the bottom of the front frame. Ab Lounge™ exercise products with straight brackets that do not fold are not part of this recall.. Recalled by Fitness Quest Inc., of Canton, Ohio. Units affected: About 460,000.
Why was this product recalled? ▼
When opening or folding up these exercise machines, consumers can catch their fingers in the hinges. This can result in lacerations, crushing, or amputation to fingertips. This does not occur while users are exercising.
What should consumers do? ▼
Firm no longer in business. Recall remedy no longer available. Discard the product. Do not donate or resell.
Which agency issued this recall? ▼
This recall was issued by the CPSC on November 23, 2004. Severity: Moderate. Recall number: 05055.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (05055) 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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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: CPSC, reported November 23, 2004. 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.