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All product recalls associated with Neuro-Fitness LLC.
Total Recalls
1000
Past Year
1000
Class I (Serious)
143
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.
No FDA clearance for the .35Hz/.45Hz frequency option on device.
Incorrect Results -- Through evaluation of stability, Abbott have found a decrease in the calibrator A to F span with these reagents lots, which may produce the following results: - Printed Error Code "SPAN LESS THAN MIN SPAN" - Controls out of range. When a control is out of range, patient results should not be reported.
Incorrect Results -- Through evaluation of stability, Abbott have found a decrease in the calibrator A to F span with these reagents lots, which may produce the following results: - Printed Error Code "SPAN LESS THAN MIN SPAN" - Controls out of range. When a control is out of range, patient results should not be reported.
Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head.
Incorrect part: Device may have an incorrect locking ring assembled with the UHR bipolar head.
Incorrect Results -- Through evaluation of stability, Abbott have found a decrease in the calibrator A to F span with these reagents lots, which may produce the following results: - Printed Error Code "SPAN LESS THAN MIN SPAN" - Controls out of range. When a control is out of range, patient results should not be reported.
Incorrect Needle size - Some of the kits contain a 1 inch 21G needle instead of the 1-1/2 inch 21G needle specified on the kit label.
Sample/Patient Mis-identification: Two issues identified related to the ACCELERATOR Decision Manager (ADM), to include: 1) Sample Identification (SID) and/or Patient Identification (PID) numbers that contain more than 12 characters are truncated to the final 12 characters by the ADM; 2) for SIDs using alpha characters that are case sensitive, SIDs with lower case characters are transmitted by the
This recall involves the Robbie Ducky children's leaf rake, hoe, broom and spade. "Robbie Ducky™ Garden Collection" is printed on a tag attached to the handle. The rake has a yellow handle with the head of a tortoise and green prongs. The hoe has an orange handle with a caterpillar and a blue blade. The broom has a purple handle with a duck and an orange brush. The spade has a yellow handle with the head of a frog and a red blade. The tools measure between 27 and 29 inches long.
Sterility (package integrity) compromised: This recall is being conducted due to incomplete seal of the product package at the corner of the outer tray and tyvek lid.
The bottom of the children's seat is round and flat with a diameter of about 15 inches. It is constructed of a single piece of molded foam and comes in yellow, blue, purple, pink, aqua, and lime green. The seat has leg holes and seat back that wraps completely around the child. On the front of the seat in raised lettering is the word "Bumbo" with the image of an elephant on top. The bottom of the seat has the following words: "Manufactured by Bumbo South Africa Material: Polyurethane World Patent No. PCT: ZA/1999/00030." The back of the seat contains the following "WARNING" - "Never use on a raised surface. Never use as a car seat or bath seat. Designed for floor level use only. Never leave your baby unattended as the seat is not designed to be totally restrictive and may not prevent release of your baby in the event of vigorous movement."
The 2006 Line X-Fly and Line Pro model ski boards were sold in 90- and 99-centimeter lengths. The Pro model is a twin-tip ski which is turned up at both ends. "Pro 90" or "Pro 98" is printed on the tail. The X-Fly is a unidirectional ski which is turned up on one end. "Fly 90" or "Fly 99" is printed on the tail.
This recall involves the Reynolds UL bicycle fork models with 43 mm and 50 mm rakes and with serial numbers 09100 through 10403. The serial number decal is located on the steer tube. To see the serial number, the fork must be removed from the frame. Some recalled forks are black, have "Reynolds" printed on them, and have a gray and white stripe painted on the legs of the fork. Other recalled forks were painted with a different paint scheme and do not have "Reynolds" printed on them. To determine if a fork is included in this recall, consumers should contact the company.
This recall involves the 64 Zone Wireless Receivers with model 45A00-1 and revision number B1. The receiver is an accessory to the Home Automation Inc. Home Control System and is professionally installed. The model and revision numbers can be found on a label on the back of the unit.
This recall involves the treadmills "Cybex 400T," "Cybex 410T," "Trotter 510," "Trotter 525", "Trotter 535", and "CXT+" that were recalled on October 8, 2003 and later repaired. The treadmills are black with gray coloring, have rectangular uprights, and measure 69 inches long and 30 inches wide. The brands and models are written on the display panel. The "CXT+" model does not bear the brand Cybex or Trotter.
The Salicylate Reagent lots listed here may fail calibration and/or fail to maintain linearity at the upper end of analytical range.
This recall involves the battery-operated power pack boxes for the 20-gallon "Sports Cool Powered Team Drinker" and the 40-gallon "Sports Cool Powered Tanker with Cart" portable team hydration units. The units include a water tank, six hoses, a battery-operated pack box, and a cart. "Sports Cool" is printed on the water tank.
Incorrect dose data: GE Healthcare has found that after 6 days and 4 hours without performing a system reset or a system reboot (turning it off/on), the displayed dose data on these systems (Innova 3100 / Innova 4100 with Bolus option) may be underestimated by up to 50%. In order to avoid this issue, it is necessary to perform a system reset or reboot every day. GE Healthcare is working on a c
Incorrect dose data: GE Healthcare has found that after 6 days and 4 hours without performing a system reset or a system reboot (turning it off/on), the displayed dose data on these systems (Innova 3100 / Innova 4100 with Bolus option) may be underestimated by up to 50%. In order to avoid this issue, it is necessary to perform a system reset or reboot every day. GE Healthcare is working on a c
Pneumatic Leaks: air leaks developing in the pneumatic driveline when subjected to excessive stress at the junction of the percutaneous line to the pump housing due to sharp bending when implanted (paracorporeal-external-position).