Severity
Moderate
Inversion Therapy Tables Recalled by Stamina Products Due to Fall Hazard
Reported: January 16, 2008 Initiated: January 16, 2008 #08538 About 2,000 units
Stamina Products Inc., of Springfield, Mo. issued this CPSC recall on January 16, 2008. Classified as Moderate severity. Approximately About 2,000 units are affected. The recall was issued because: A weld in the center of the inversion table can fail when the table is in an inverted position, posing a fall hazard to…. 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 #08538) was formally reported on January 16, 2008. It is classified under Moderate severity, with a current status of Active. Stamina Products Inc., of Springfield, Mo. is listed as the recalling firm. Federal records indicate About 2,000 units are affected.
The documented reason for this recall is: A weld in the center of the inversion table can fail when the table is in an inverted position, posing a fall hazard to consumers. 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 inversion tables immediately and contact Stamina Products to have the table picked up and to receive a free replacement inversion table or a refund. — 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 18 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
Units Affected
About 2,000
Related Recalls
6
6 from same agency
Product Description
This recall involves the following inversion therapy tables: Name Model Number Serial Number Inversion Therapy Table 55-1531 05NOV000001 through 05NOV000414 and 05DEC000415 through 05DEC000828 Pro Inversion System 55-1536, 55-1536A, and 55-1536B 05SEP000001 through 05SEP000528, 06NOV000001 through 06NOV000528, and 07SEP000001 through 07SEP000528 This exercise equipment allows consumers to fasten to the table in an upright position and safely invert. The model and serial number are located on the black Stamina label found to the left of the rubber stopper on the cross bar.
Reason for Recall
A weld in the center of the inversion table can fail when the table is in an inverted position, posing a fall hazard to consumers.
Remedy
Consumers should stop using the recalled inversion tables immediately and contact Stamina Products to have the table picked up and to receive a free replacement inversion table or a refund.
Details
- Recalling Firm
- Stamina Products Inc., of Springfield, Mo.
- Units Affected
- About 2,000
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 08538 |
| Date reported | January 16, 2008 |
| Date initiated | January 16, 2008 |
| Recalling firm | Stamina Products Inc., of Springfield, Mo. |
| Units affected | About 2,000 |
| Distribution | Not disclosed |
Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.
Frequently Asked Questions
What product was recalled? ▼
This recall involves the following inversion therapy tables: Name Model Number Serial Number Inversion Therapy Table 55-1531 05NOV000001 through 05NOV000414 and 05DEC000415 through 05DEC000828 Pro Inversion System 55-1536, 55-1536A, and 55-1536B 05SEP000001 through 05SEP000528, 06NOV000001 through 06NOV000528, and 07SEP000001 through 07SEP000528 This exercise equipment allows consumers to fasten to the table in an upright position and safely invert. The model and serial number are located on the black Stamina label found to the left of the rubber stopper on the cross bar.. Recalled by Stamina Products Inc., of Springfield, Mo.. Units affected: About 2,000.
Why was this product recalled? ▼
A weld in the center of the inversion table can fail when the table is in an inverted position, posing a fall hazard to consumers.
What should consumers do? ▼
Consumers should stop using the recalled inversion tables immediately and contact Stamina Products to have the table picked up and to receive a free replacement inversion table or a refund.
Which agency issued this recall? ▼
This recall was issued by the CPSC on January 16, 2008. Severity: Moderate. Recall number: 08538.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (08538) 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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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.
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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.
Read our methodology — how this data is sourced, computed, and verified.
All federal data sources used on this page
- U.S. Census Bureau ACS — demographic + housing + income data. census.gov/programs-surveys/acs
- BLS Occupational Employment and Wage Statistics (OEWS) — wage + employment by occupation. bls.gov/oes
- BEA Regional Economic Accounts — GDP + personal income by state/metro. bea.gov/data/regional
- U.S. Census Bureau County Business Patterns — establishment + employment by industry. census.gov/cbp
- IRS Statistics of Income (SOI) — tax-return aggregate data. irs.gov/statistics
- data.gov — U.S. federal open-data portal — discovery layer for additional federal sources. data.gov
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).