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. 2,453 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,453 in last 12 months

Showing 2632126340 of 49,677 recalls

FoodApril 20, 2018· Eden's Ethnos, LLC

Recalled Item: Eden's Ethnos Bulk Kratom 25 powder kilogram bag Also called K. Bali Supreme...

The Issue: FDA and state samples found Salmonella in Kratom products that traced back...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 20, 2018· CareFusion 303, Inc.

Recalled Item: Alaris Infusion Pump administration sets labeled as: -Infusion Set Alaris...

The Issue: Complaints where users were unable to prime the administration set.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Torax Medical, Inc.

Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...

The Issue: Possible out of specification condition which may allow a bead component to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Go.Up Recalled by Siemens Medical Solutions USA, Inc Due to There is...

The Issue: There is a potential for a software issue that may cause the need for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Now Recalled by Siemens Medical Solutions USA, Inc Due to There...

The Issue: There is a potential for a software issue that may cause the need for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Torax Medical, Inc.

Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...

The Issue: Possible out of specification condition which may allow a bead component to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Torax Medical, Inc.

Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...

The Issue: Possible out of specification condition which may allow a bead component to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Torax Medical, Inc.

Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...

The Issue: Possible out of specification condition which may allow a bead component to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Torax Medical, Inc.

Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...

The Issue: Possible out of specification condition which may allow a bead component to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugApril 19, 2018· Sun Pharmaceutical Industries, Inc.

Recalled Item: Sulfamethoxazole and Trimethoprim Tablets USP Recalled by Sun Pharmaceutical...

The Issue: Presence of Foreign Substance:Sun Pharma is recalling one (1) lot of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 19, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Gentamicin Flex reagent cartridge Recalled by Siemens Healthcare...

The Issue: The affected lots may exhibit inaccuracy for Quality Control and patient...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Gentamicin Flex reagent cartridge Recalled by Siemens...

The Issue: The affected lots may exhibit inaccuracy for Quality Control and patient...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2018· MicroAire Surgical Instruments, LLC

Recalled Item: MicroAire SmartRelease Endoscopic System Recalled by MicroAire Surgical...

The Issue: The Instructions for Use (IFU) is incorrect with regards to sterilization...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2018· Maquet SAS

Recalled Item: VOLISTA StandOP (model 600) surgical lights shipped from October 2012...

The Issue: Potential keypad failure on VOLISTA StandOP Surgical Lights.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodApril 18, 2018· NatureBox, Inc.

Recalled Item: Whole Wheat Chocolate Animal Cookies Recalled by NatureBox, Inc. Due to...

The Issue: While packing from a bulk bin of whole wheat chocolate animal cookies, 2...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodApril 18, 2018· Viable Solutions, LLC

Recalled Item: Mitragyna Speciosa Leaf Powder-GREEN Horn Recalled by Viable Solutions, LLC...

The Issue: Mitragyna Speciosa Leaf Powder Green Horn Kratom product is being recalled...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 18, 2018· Viable Solutions, LLC

Recalled Item: Mitragyna Speciosa Leaf Powder-Thai Maeng Da Recalled by Viable Solutions,...

The Issue: Mitragyna Speciosa Leaf Powder Thai Maeng Da Kratom product is being...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 18, 2018· Viable Solutions, LLC

Recalled Item: Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa...

The Issue: Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa Leaf...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 18, 2018· Canon Medical System, USA, INC.

Recalled Item: DRAD-3000E (Radrex-i) TFP-4336W (Wireless FPD) Recalled by Canon Medical...

The Issue: It was found when an operator performs a radiography using the wireless flat...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugApril 17, 2018· Rhodes Pharmaceuticals, L.P.

Recalled Item: Aptensio XR (methylphenidate HCl extended-release) capsules 15 mg Rx Only...

The Issue: Failed Dissolution Specification: Low dissolution outside of specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund