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Land America Health and Fitness Co., of China

Land America Health and Fitness Co., of China Recalls

All product recalls associated with Land America Health and Fitness Co., of China.

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Recall Summary

Total Recalls

1000

Past Year

593

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 9141–9160 of 10391 recalls

F3 Exercise Units (Nautilus) – fall risk (2009)

This recall involves Nautilus F3 Chin Dip stationary exercise units. The model number (F3CD) is located on the frame of the product.

CPSCAug 13, 2009Nationwide• Land America Health and Fitness Co., of China

Workshop Sets (Little Tikes) – choking hazard (2009)

Choking Hazard

The oversized, plastic toy nail is about 3 inches long by 1 inch in diameter and comes in red or blue colors. It has a large round head; about 1 ¼ inches below the head is a plastic ridge, slightly smaller than the nail head and about 1 inch in diameter. They were sold with a variety of Little Tikes Children's products. The names, model numbers and UPC code of the products included in this recall are listed below: Model # Name 0914/430B Electronic Project Workshop SOLD FROM MARCH 1994 THROUGH DEC 2003 UPC: 0-50743-00914-3 UPC: 0-57043-52613-8 0920/612237 Little HandiWorker Workhorse SOLD FROM MARCH 1999 THROUGH JUNE 2009 UPC 0-50743-10920-1 UPC 0-50743-61223-7 4146 Home Improvements 2-Sided Workshop SOLD FROM FEBRUARY 2001 THROUGH JANUARY 2009 UPC 0-50743-04146-4 440Z Swirlin' Sawdust Workshop SOLD FROM APRIL 2004 THROUGH NOVEMBER 2008 UPC 0-50743-38540-7 4028 Black Pickup Truck with Tools SOLD FROM MARCH 2000 THROUGH APRIL 2009 UPC 0-50743-04028-3

CPSCAug 13, 2009Nationwide• Little Tikes, of Hudson, Ohio

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The Anspach Effort, Inc.: Foot Pedal, Foot Control for SC2000 and SC2100 Powered, s...

The Anspach Effort, Inc. is recalling the Foot Control/ Foot Pedal for SC2000 and SC2100 Powered, simple cranial drills, burrs, trephines, and accessories. The Foot Control Cables lacks the shield connection from the cable to the connector body. The lack of shielding may result in radiated emissions which could possibly cause interference on other electrical equipment adjacent to the foot pedal

FDAAug 13, 2009Nationwide• The Anspach Effort, Inc.

Ge Healthcare: GE OEC 9900 Elite GSP Fluoroscopes To produce mobile flu...

A software defect - may result in a false indication and warning on the OEC 9900 Workstation and C-arm display that the X-Ray tube Anode is over-heated. This will also cause the displayed air kerma rate and cumulative air kerma to be inaccurate.

FDAAug 12, 2009Nationwide• Ge Healthcare

Ge Healthcare: GE OEC 9900 Elite ESP To produce mobile fluoroscopic im...

FDAAug 12, 2009Nationwide• Ge Healthcare

Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany: BrainLab Radiotherapy Treatment Planning Software; Cata...

Failure to conduct important safety checks when using the BrainLab radiotherapy treatment planning software in combination with BrainLab conical collimators could result in unintended radiation outside the conical shaped field, which may lead to serious injury of the patient.

FDAAug 12, 2009Nationwide• Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany

Ossur H F Grjothals 5 Reykjavik Iceland: Total Knee Junior Model Number 1100 Product Usage: The T...

Some units of the Total Knee Junior produced between November 25th, 2008 and through April, 2009 contain balancing units that may fail under extreme use over a long period. The fault is noncritical and no incidents or injuries resulting from this situation have been reported to Ossur at this stage. Over long term use (estimated to be in the four to six year range) the prosthetic device may fail a

FDAAug 10, 2009Nationwide• Ossur H F Grjothals 5 Reykjavik Iceland

GE Healthcare, LLC: Innova 2000 The principle system components include a C-a...

GE Healthcare has become aware of a potential video splitter failure with certain Innova 2000 and 4100 X-ray systems that may impact patient safety. A potential video splitter failure inside the GE equipment cabinet could occur with no advance warning and thereby prevent x-ray image display. Should this occur, the system cannot be recovered without service intervention. GE Healthcare has obse

FDAAug 6, 2009AL, AZ, CA +39 more• GE Healthcare, LLC

GE Healthcare, LLC: Innova 4100/4100IQ GE Innova 4100 / 4100 IQ. , GE Healthc...

FDAAug 6, 2009AL, AZ, CA +39 more• GE Healthcare, LLC

GE Healthcare, LLC: Innova 2121-IQ/3131--1Q Biplane Cardiovascular Imaging Sy...

GE Healthcare has become aware of a potential issue regarding Innova systems with GE Fluoro UPS 20KVA that may impact patient safety. GE Fluoro UPS 20KVA (Uninterrupted Power Supply) is used to maintain fluoroscopy availability for approximately 5 minutes should there be a main power failure. Once power is restored, the equipment power will be returned to the main hospital power. UPS fluoro ba

FDAAug 5, 2009AL, AZ, AR +39 more• GE Healthcare, LLC

GE Healthcare, LLC: Innova 2100IQ (The Digital Fluoroscopic Imaging System co...

FDAAug 5, 2009AL, AZ, AR +39 more• GE Healthcare, LLC

GE Healthcare, LLC: Innova 3100/3100IQ GE Innova 3100 / 3100 IQ, Cardiovascul...

FDAAug 5, 2009AL, AZ, AR +39 more• GE Healthcare, LLC

Baxter Healthcare Corp.: Baxter's elastomeric infusion pumps are non-electronic, a...

There are reported incidents of leakage on the INFUSOR and FOLFUSOR pumps at the connection of the blue winged cap and the distal male Luer. Investigation of these reports indicates the incidence of leakage has only occurred after pumps are filled, primed, re-capped (using the blue winged Luer cap) and stored for a period of time, typically overnight. In addition, the reported instances of leakage

FDAJul 31, 2009Nationwide• Baxter Healthcare Corp.

Baxter Healthcare Corp.: Baxter's elastomeric infusion pumps are non-electronic, a...

Class IIModerate

FDAJul 31, 2009Nationwide• Baxter Healthcare Corp.

Baxter Healthcare Corp.: Baxter's elastomeric infusion pumps are non-electronic, a...

Class IIModerate

FDAJul 31, 2009Nationwide• Baxter Healthcare Corp.

Baxter Healthcare Corp.: Baxter's elastomeric infusion pumps are non-electronic, a...

Class IIModerate

FDAJul 31, 2009Nationwide• Baxter Healthcare Corp.

Little Tikes Clubhouse Swing Set (Little Tikes) – fall hazard (2009)

The Little Tikes Clubhouse Swing Set is a plastic molded product that features a climbing wall, rope ladder, slide and two swings with blue and yellow seats. Only the blue seat model is being recalled. The model numbers are 400V and 612398.

CPSCJul 30, 2009Nationwide• Little Tikes, of Hudson, Ohio

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Virtuoso VR, Model D154VWC, Single Chamber impl...

Medtronic has detected a specific pattern of MOSFET IC malfunctions in its Concerto, Virtuoso and EnRhythm family of devices. The probability of occurrence decreases with time and, to date over 90% of the malfunctions related to the pattern have occurred within the first twelve months after implant.

FDAJul 27, 2009Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Virtuoso DR, Model D154AWG, Dual Chamber implan...

FDAJul 27, 2009Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Spacelabs Healthcare, Incorporated: Spacelabs Medical Integrated ECG Cable are supplied as pa...

The Spacelabs Medical Integrated ECG Cables, PN: 700-0008-22, 700-0008-23, 700-0008-24, and 700-0008-25 will not withstand the high voltage of a defibrillation shock.

FDAJul 23, 2009Nationwide• Spacelabs Healthcare, Incorporated