Severity
Moderate
The recall
issued this moderate-severity CPSC recall — The pneumatic lifting mechanism can pinch or break fingers during assembly or use, posing a risk of serious i….
Sourced from official CPSC enforcement records. Verify recall #16750 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This CPSC action (record #16750) was formally reported on June 2, 2016. It is classified under Moderate severity, with a current status of Active. The recalling firm is not specified in the federal record. Federal records indicate About 750 units are affected.
The documented reason for this recall is: The pneumatic lifting mechanism can pinch or break fingers during assembly or use, posing a risk of serious injury. 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 immediately stop using the recalled converters and contact the firm for a free repair kit. — 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 and NHTSA going back to 1995. Within the same product category, the database holds 6 closely related recalls. 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 10 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.
Of 83,949 recalls in the database, 21,198 are high severity, 58,883 moderate, and 3,868 low. This recall is classified moderate severity.
Severity
Moderate
Units Affected
About 750
Related Recalls
6
0 from same agency
This recall involves Square Grove's Sit-Stand Converters. The model included in the recall is UPL147 and includes the freestand and clamp versions. The freestand version sits on a desk that raises and lowers a computer monitor and keyboard by 17 inches. The clamp version functions the same, but clamps to the back of the desk. The color of both versions is black. The dimensions for the top platform are about 24 inches in width and 16 inches in diameter. The keyboard platform dimensions are about 24 inches in width and 9 inches in diameter. The freestanding base platform version dimensions are about 20 inches in width and 20 inches in diameter. The clamp mount version dimensions are about 7 inches in width and 18 inches in diameter. The words "UPLIFT DESK" are printed on the product.
The pneumatic lifting mechanism can pinch or break fingers during assembly or use, posing a risk of serious injury.
Consumers should immediately stop using the recalled converters and contact the firm for a free repair kit.
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 16750 |
| Date reported | June 2, 2016 |
| Date initiated | June 2, 2016 |
| Recalling firm | Not disclosed |
| Units affected | About 750 |
| Distribution | Not disclosed |
Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.
Learn how the US recall system works and how to protect yourself and your household.
How the US Recall System Works
The three federal agencies, how recalls are initiated, and what happens next.
Understanding Recall Severity Classes
What Class I, II, and III mean and which recalls demand immediate action.
What to Do When a Product Is Recalled
Verify, claim your remedy, report injuries, and navigate the process.
How to Check If Your Products Are Recalled
Step-by-step guide to checking food, products, medications, and vehicles.
Recalled Products in Your Home
A room-by-room household audit guide for active recalls.
Most Recalled Product Categories
Rankings of highest-recall categories from FDA, CPSC, and NHTSA.
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.
Explore related product safety and public health data from federal sources.
Food Safety Inspections
FDA and state food facility inspection results — violations, enforcement actions, and compliance history for food manufacturers and processors.
PlainFoodSafe →
Ingredient Safety Data
FDA food additive and ingredient safety database — regulatory status, usage limits, and safety assessments for thousands of ingredients.
PlainIngredients →
Nutrition Data
USDA nutrition facts for 2M+ food items — calories, macros, vitamins, and ingredient analysis to verify what you consume.
GetFoodFacts →
Drug Safety Information
FDA drug data for 680+ medications — interactions, alternatives, side effects, and safety information for recalled and active drugs.
PlainMeds →
Product Injury Data
CPSC emergency room injury data for 838 product categories — 7.3M NEISS records tracking real-world consumer product injuries.
PlainSafety →
Recall Checker
Search our database of 83K+ recalls by product name, brand, or recall number across all agencies.
Check Now →
Recall Radar
Live feed of the latest recalls across FDA, CPSC, NHTSA, and USDA — filter by agency and severity.
View Radar →
Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.
Waldemar Link GmbH & Co. KG (Mfg Site) · 2026-03-18
Penner Patient Care, Inc. · 2026-03-18
Instrumentation Laboratory · 2026-03-18
Beckman Coulter Mishima K.K. · 2026-03-18
Trividia Health, Inc. · 2026-03-18
Compare this recall with Endo-Model Replacement Plateau; Item Number: 15-0027/11; →
Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.
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.
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).