CPSCMay 10, 2006consumer
American Innovations Corp. Recalls Ladder Extensions that Can Detach and Hit Consumers
Official recall recorded by the U.S. Consumer Product Safety Commission.
The hazard
If the knob securing the extension unit to the ladder is not tight, it can detach and fall when the ladder is being removed or lowered. The unit could hit a bystander, causing serious head injuries.
What to do
Owners are being sent a free repair kit, including a safety strap and easy-to-follow assembly instructions. Until the repair is made, consumers should check to make sure the knob securing the extension unit is tight during use.
Brands named
walkwalk throughamericanamerican innovations
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- CPSCMerkury Innovations Recalls Hot + Cool Heating and Cooling Fans Due to Risk of Serious Injury or Death from Fire Hazard2026-06-11
- CPSCArctic Zone Titan Pro Coolers Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Imported by California Innovations and Sold at Costco2026-06-11
- CPSCLithium Coin Batteries Recalled Due to Battery Ingestion; Violates Federal Statute for Child-Resistant Packaging of Coin Batteries; Imported by Proudly American Store, of Canada2026-05-28
- FDARoast beef and cheddar closed face sandwich packed in clear plastic wrap with a green adhesive label. The label reads in part as "***Lunch Box Kitchen*** Premium Convenience***Turkey & Cheddar Sub***BEST BY 06/14/26 Lot no. 26 134 NET WEIGHT: 6.1oz***KEEP REFRIGERATED*** Produced by: Produce Inno...2026-05-27
- CPSCAmerican Honda Motor Recalls Off-Road Motorcycles Due to Risk of Serious Injury or Death Due to Crash Hazard2026-04-30
- FDAArvis Hip & Knee 2.0 Instrument Set, REF: IN-21200 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C2026-04-23
- FDAArvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C; IN-28050, Tracker E2026-04-23
- FDALevocarnitine Injection, USP, 1 g/5 mL (200 mg/mL), 5 mL Single-Dose Vial, For intravenous use, Rx Only, American Regent, Inc., Shirley, NY 11967. NDC: 0517-1045-012026-04-16
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