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All product recalls associated with Medtronic Inc.
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.
Medtronic has identified an issue with the labeling of the I-4500 Silicone Oxygenators (P/N 61399402655). Lot numbers of this oxygenator manufactured between August 2007 and September 2008 have an incorrect "Recommended maximum blood flow range" on the label. The label on the device states a range of 5.0 - 8.5 L/min but should state a range of 5.0 - 6.5 L/min. These oxygenators are acceptable t
These devices may experience difficulty cocking and arming, resulting in an inability to use the devices.
These devices may experience difficulty cocking and arming, resulting in an inability to use the devices.
The recalled walkers were sold for babies 6 months and older. The walkers were sold in the following colors: pink, red, green, blue, and ivory. The walkers have an activity tray with a steering wheel and other toys. "My Way Corp" is printed on a sticker on the front of the walker.
Catheter pouch was mislabeled with the wrong size.
GE initiated a correction to the instructions/use due to the potential for erroneous auto injection of contrast dye.
GE initiated a correction to the instructions/use due to the potential for erroneous auto injection of contrast dye.
The recall involves Effikal RVGP-PC Gas Vent Damper size 4, 5, 6, 7, 8, 9, or 10 which are installed with the gas boiler systems listed below. The vent damper date code is located on a sticker under the motor assembly cap on the plastic base. Serial numbers are located on a label on the side of the damper's cap. All sizes and models of the RVGP-PC have the same motor assembly with black Effikal caps and black plastic bases. Manufacturer Atmospheric Gas Boiler Models Vent Damper Date Codes Vent Damper Serial Numbers Allied Engineering MG, MS and SG Series 0728 through 0809 3588428 through 3687571 Burnham Series 2b, Series 8h, and Independence except Independence PV 0728-0738 3588428-3647820 Crown AWI, CWI and BSI Series 0728-0809 3588428-3687571 Hydro Therm R/MR, VGA, VS and HW Series 0728-0809 3588428-3687571 Laars JV Series 0728-0809 3588428-3687571 Lochinvar CBN Solution Series 0728-0809 3588428-3687571 RBI Spectrum Series 0728-0809 3588428-3687571 Smith GB and HW Series 0728-0809 3588428-3687571 New Yorker CG and CGS Series 0728-0738 3588428-3647827 Peerless MI, 63 and GM series 0728-0809 3588428-3687571 Raypak Series XV-42-180 Series V-181-260 and 182-261 Series VII-133 0728-0809 3588428-3687571 Union Steam GWA and GSA 0728-0809 3588428-3687571 Weil-McLain CGa, EG, and PFG Series 0728-0738 3538074-3647830 WilliamsonThermoflo GWA and GSA s 0728-0738 3538074-3647830
Product is mislabeled as having a shelf life of 3 years, where the actual shelf life is 1 year.
It has come to our attention that users of these product lots may experience an elevation in the rate of false positivity when compared with previous product lots. Internal quality assurance testing has shown that the products are performing within the release specifications, although there has been a slight shift in the cut-off which may lead to an increase in the number of positive results obta
The recall involves YO-YO amusement rides, consisting of a vertical cylinder with rotating horizontal sweep arms, from which the riding chairs hang.
Packaging issue may result in failure to maintain sterile barrier.
Boston Scientific Corporation initiated a recall of its easy Core" BIOPSY SYSTEM due to difficulty cocking or arming the cannula latch on the device. This difficulty may result in an inability to use the device.
Failure to insert the guidewire through the 18 gauge introducer needle
Failure to insert the guidewire through the 18 gauge introducer needle
Failure to insert the guidewire through the 18 gauge introducer needle
Failure to insert the guidewire through the 18 gauge introducer needle
Poor sensitivity and imprecision on ADVIA Centaur systems; Serum samples low bias; EDTA plasma samples low bias
May experience an interruption of ventilation for approximately 5 seconds
Biosense Webster initiated the recall because of the potential concern with one of the Printed Circuit Board (PCB) components used in the NaviStar RMT Catheters, which may cause the ablation catheter icon to shift on the map viewer when RF energy is being applied. Therefore the user, attempting a linear ablation in the location displayed on the CARTO RMT screen, may ultimately apply RF energy to u