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All product recalls associated with Sybaritic, Inc.
Total Recalls
1000
Past Year
566
Class I (Serious)
25
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.
A correction or removal, conducted to reduce a risk to health posed by a device, was not reported in writing to FDA. Sybaritic, Inc. conducted a recall on DERMALIFE 2G equipment (SpaJet, Spa Oceana, Spa Feng Shui) because of IR Fan failure which resulted in the overheating and failure of the IR emitter and surrounding assembly.
A correction or removal, conducted to reduce a risk to health posed by a device, was not reported in writing to FDA. Sybaritic, Inc. conducted a recall on DERMALIFE 2G equipment (SpaJet, Spa Oceana, Spa Feng Shui) because of IR Fan failure which resulted in the overheating and failure of the IR emitter and surrounding assembly.
The transducer adapter bracket on the pump could crack or break and potentially result in under delivery of the enteral product.
Continued use of the pump may cause the door pivot point on the back of the pump to crack or break. This will cause the pump to shut down and stop the initiation of enteral feeding.
Falsified Repair/Test and Inspection records: Pumps submitted for repair or service may not have been properly repaired or serviced before being returned to the customer.
Falsified Repair/Test and Inspection records: Pumps submitted for repair or service may not have been properly repaired or serviced before being returned to the customer.
Falsified Repair/Test and Inspection records: Pumps submitted for repair or service may not have been properly repaired or serviced before being returned to the customer.
Falsified Repair/Test and Inspection records: Pumps submitted for repair or service may not have been properly repaired or serviced before being returned to the customer.
A software anomaly is causing newly upgraded Colleague Triple Channel Infusion Pumps to alarm, display an error code (16:310:867:0002) and stop the infusion. This occurs during user programming with all three channels simultaneously infusing fluids. In reported cases, the pump stopped infusing and both an audible and a visual alarm notification were activated.
ACL TOP unit, when in emergency stop may release liquid during recovery sequence and contaminate sample tube.
It has been determined that with low probability, over-infusion may occur as a result of an open safety clamp fitment (a.k.a. Flo-Stop fitment) on the pumping segment, whether opened intentionally in the course of expected clinical practice, or as a result of inadvertent action. The over-infusion occurrence is dependent on the user not closing the roller clamp first, as required by clinical practi
The recall includes snow equipment with Briggs & Stratton OHV engines that have model numbers beginning with 12, 15, 20, or 21, and a date of manufacture (DOM) code between 000601xx and 070301xx. The engines were installed on the following brand snow throwers: Ariens, Canadiana, Craftsman, Frontier Equipment, Husqvarna, Poulan Pro, Simplicity and Snapper. The engine model number and DOM information are located on the cylinder shield or rocker cover. Call for more information about determining if your snow thrower engine is included in the recall.
Mislabeling: Product is labeled with the wrong expiration date: 2009-12. The correct expiration date is 2008-12.
The cooktop has electric and induction heating elements with a black ceramic glass surface. This recall involves model numbers CIT302DS/01 and CIT362DS/01 with date codes between 8606 and 8612. The model number and date code can be found on the underside of the cooktop.
The recalled Baby Long Johns are red with snap fasteners down the front and along the legs. A personalized embroidery is stitched across the button-up back flap on the long johns. The long johns were sold in sizes 6, 12, 18 and 24 months.
Incorrect Unit of Measure displayed : The meters report results in the wrong unit of measurement for Canadian users.
The sterility of the product may be compromised as the packaging used for the sterility barrier was not designed for the sterility process used by the firm.
Target Alignment Error : A mechanical component/software incompatibility caused by a specific combination of the BrainLAB Target Positioner version 40700-3A for Leksell headrings and BrainLAB planning software resulted in a 1.25 mm shift in target area alignment during radiosurgery treatment.
Labels on the carton from two batches/lots of Impulse Angiographic Catheters may indicate a different curve style than the device that is actually in the carton.
The tubes may kink during use which may impede or prevent ventilation.