PlainRecalls

CPSC, Nautilus Direct Announce Recall of Bowflex Power Pro Fitness Machines

Reported: January 29, 2004 Initiated: January 29, 2004 #04073 About 420,000 units

Nautilus Direct (doing business as Bowflex), of Vancouver, Wash. issued this CPSC recall on January 29, 2004. Classified as Moderate severity. Approximately About 420,000 units are affected. The recall was issued because: First, while being used in the incline position, the machine's backboard bench can unexpectedly collapse and break, pos…. This recall notice is sourced from official CPSC enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.

Recall Insight

This CPSC action (record #04073) was formally reported on January 29, 2004. It is classified under Moderate severity, with a current status of Active. Nautilus Direct (doing business as Bowflex), of Vancouver, Wash. is listed as the recalling firm. Federal records indicate About 420,000 units are affected, a scale large enough to require multi-state distribution tracking.

The documented reason for this recall is: First, while being used in the incline position, the machine's backboard bench can unexpectedly collapse and break, posing a risk of injury to the user. Second, the "Lat Tower," can rotate forward and fall during use, p… 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 backboard bench in the incline position and "Lat Tower" on the fitness machines immediately. The firm is no longer in business and the recall remedy is no longer avail… — consumers holding this product should act on that instruction rather than relying on general guidance.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 6 were also issued by CPSC. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 22 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.

Recall Distribution by Severity Class

Severity1Class I (Critical)Class II (Moderate)Class III (Low)
Recall Distribution by Severity Class

Severity

Moderate

Units Affected

About 420,000

Related Recalls

6

6 from same agency

Product Description

The recalled fitness machines are the Bowflex Power Pro XL, XTL and XTLU systems with the "Lat Tower" attachment. The "Lat Tower" attaches to the back of the bench, and has pull-down pulleys attached. The name "Bowflex" and the model name are printed on the front of the machine. The machine has 10 to 14 resistance rods that extend about 48 inches high and a backboard bench that is about 36 inches long.

Reason for Recall

First, while being used in the incline position, the machine's backboard bench can unexpectedly collapse and break, posing a risk of injury to the user. Second, the "Lat Tower," can rotate forward and fall during use, posing a risk of injury to the user.

Remedy

Consumers should stop using the backboard bench in the incline position and "Lat Tower" on the fitness machines immediately. The firm is no longer in business and the recall remedy is no longer available. Discard this product. Do not donate or resell.

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 04073
Date reported January 29, 2004
Date initiated January 29, 2004
Recalling firm Nautilus Direct (doing business as Bowflex), of Vancouver, Wash.
Units affected About 420,000
Distribution Not disclosed

Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.

Scale of Impact

About 420,000 units affected — multi-state distribution scale.

Regional (<10K units)
Multi-state (10K – 100K units)
Large-scale (100K – 1M units) ✓ This recall
Massive (≥1M units)

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Consumer Product Safety Commission filings.

Frequently Asked Questions

What product was recalled?
The recalled fitness machines are the Bowflex Power Pro XL, XTL and XTLU systems with the "Lat Tower" attachment. The "Lat Tower" attaches to the back of the bench, and has pull-down pulleys attached. The name "Bowflex" and the model name are printed on the front of the machine. The machine has 10 to 14 resistance rods that extend about 48 inches high and a backboard bench that is about 36 inches long.. Recalled by Nautilus Direct (doing business as Bowflex), of Vancouver, Wash.. Units affected: About 420,000.
Why was this product recalled?
First, while being used in the incline position, the machine's backboard bench can unexpectedly collapse and break, posing a risk of injury to the user. Second, the "Lat Tower," can rotate forward and fall during use, posing a risk of injury to the user.
What should consumers do?
Consumers should stop using the backboard bench in the incline position and "Lat Tower" on the fitness machines immediately. The firm is no longer in business and the recall remedy is no longer available. Discard this product. Do not donate or resell.
Which agency issued this recall?
This recall was issued by the CPSC on January 29, 2004. Severity: Moderate. Recall number: 04073.
How do I check if my product is affected by a recall?
Check the product description and recall number (04073) 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.

Recall Context

Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as moderate severity, indicating the product may cause temporary or medically reversible health consequences. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.

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

Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.

  • 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)
  • Source: USDA FSIS — Food Safety and Inspection Service (meat, poultry, and egg product 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.

All federal data sources used on this page

Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).