Product Recalls in Utah
Product recalls affecting Utah — including food, drugs, consumer products, medical devices, and vehicles distributed to Utah. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,639 recalls have been distributed to Utah in the last 12 months.
Showing 5741–5760 of 28,579 recalls
Recalled Item: Stryker ACM (Advanced Cement Mixing) System: ACM Kit w/ Femoral Recalled by...
The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT Chemistry Products ALKP Slides Recalled by Ortho-Clinical...
The Issue: Samples containing high levels of ALKP (or an interfering substance) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT Chemistry Products TBIL-ALKP Slides Recalled by Ortho-Clinical...
The Issue: Samples containing high levels of ALKP (or an interfering substance) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DJO Surgical: Empowr Knee Recalled by Encore Medical, LP Due to Orthopedic...
The Issue: Orthopedic device components were not subjected to final sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DJO Surgical: Delta Ceramic Femoral Head Recalled by Encore Medical, LP Due...
The Issue: Orthopedic device components were not subjected to final sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DJO Surgical: CLP Hip Recalled by Encore Medical, LP Due to Orthopedic...
The Issue: Orthopedic device components were not subjected to final sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DJO Surgical: Reverse Shoulder System (RSP) Semi Humeral Socket Insert...
The Issue: Orthopedic device components were not subjected to final sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DJO Surgical: Altivate Reverse Recalled by Encore Medical, LP Due to...
The Issue: Orthopedic device components were not subjected to final sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI Addipak Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Product dispositioned for scrap for sterility failure investigation that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOVAPLUS GAMMEX NON-LATEX PI GREEN Surgical gloves Recalled by Ansell...
The Issue: Some surgical glove sterile pouches were not completely sealed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3T Heater Cooler System Recalled by LivaNova Deutschland GmbH Due to The...
The Issue: The firm's labeling (Quick Guide) contains incorrect information in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GAMMEX NON-LATEX PI GREEN Surgical gloves Recalled by Ansell Healthcare...
The Issue: Some surgical glove sterile pouches were not completely sealed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE STERILE IRIS SCISSORS CVD/STD Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: 4.5" Iris Scissors, Sterile, Curved (DYNJ04049) are being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Upper roller bracket (part number 1088370) for the Gen2 gantry Recalled by...
The Issue: It is possible the upper roller bracket in the Radixact System gantry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT Recalled by Philips Healthcare Due to Philips has identified...
The Issue: Philips has identified three software issues with compliance concerns to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GS70H Salus Surgical Table Recalled by Skytron, LLC Due to When the control...
The Issue: When the control of the operating table was used in Bluetooth mode, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GS70 Salus Surgical Table Recalled by Skytron, LLC Due to When the control...
The Issue: When the control of the operating table was used in Bluetooth mode, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnifuse Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to The...
The Issue: The incorrect product labeling was applied to the product indicating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were reporting that the device was not charging as expected. It was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were reporting instances of "Gas Loss in IAB Circuit" and "Gas Gain in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.