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All product recalls associated with Medtronic Perfusion Systems.
Total Recalls
1000
Past Year
1000
Class I (Serious)
34
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.
Some warehouse inventory of Custom Pack product bags were found with ruptured seals. The seals were partially opened in the center of the bag's Tyvek edge. Since this bag is used to enclose and seal the custom pack assembly & had been sterilized, the ruptured seal breaches the sterility barrier for the package.
The product is a non-motorized two-wheeled scooter with a folding hinge and an adjustable handlebar. The scooter platform is purple with a bright pink Bratz logo on the top surface. Scooters containing information identifying the product as Item No. 266563, with a date of manufacture prior to July 2004, and manufactured by Jurong Dumar Bicycle, Inc. are included in this recall. This identification information can be located either in the area directly beneath the scooter platform or at the bottom of the scooter near the rear wheel.
The recalled includes 2005 Arctic Cat 500 and 650 FIS, and 400 and 500 TBX model ATVs. The FIS models affected by this recall have the vehicle identification number (VIN) ranges of 4UF05ATV15T226237 through 4UF05ATV15T242874, and 4UF05ATV55T246510 through 4UF05ATV55T248189. The TBX models have VIN ranges of 4UF05ATV15T221345 through 4UF05ATV15T223967, and 4UF05ATVX5T251024 through 4UF05ATV55T251397. The VIN is located on the left rear frame tube of the vehicle near the upper shock mount. AFFECTED MODELS: 2005 500 4x4 Auto LE 2005 500 4X4 Auto 2005 500 4X4 Manual 2005 650 V2 4X4 Auto 2005 650 V2 4X4 Auto LE 2005 400 4x4 Auto TBX 2005 500 4X4 Auto TBX