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. 2,375 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,375 in last 12 months

Showing 4240142420 of 49,677 recalls

Medical DeviceApril 30, 2014· Mako Surgical Corporation

Recalled Item: Robotic Arm Interactive Orthopedic System (RIO) Recalled by Mako Surgical...

The Issue: Revision of the field manual

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2014· Microport Orthopedics INC.

Recalled Item: PATH(R) THREAD CUP ADAPTOR Recalled by Microport Orthopedics INC. Due to...

The Issue: Difficulty removing the cup adaptor from the impaction handle during surgery

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

Class II — Potential Health HazardOngoing
DrugApril 29, 2014· Independent Nutrition Center, Inc.

Recalled Item: Red Yeast Rice High Potency Dietary Supplement Recalled by Independent...

The Issue: Marketed Without An Approved NDA/ANDA: Product is being recalled due to...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 29, 2014· Flawless Beauty LLC

Recalled Item: Tatiomax (reduced glutathione/hydrolyzed collagen) powder for injection...

The Issue: Marketed Without An Approved NDA/ANDA: Product is sold over the counter...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 29, 2014· Flawless Beauty LLC

Recalled Item: Sterile Water for Injection Recalled by Flawless Beauty LLC Due to Marketed...

The Issue: Marketed Without An Approved NDA/ANDA: Product is sold over the counter...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 29, 2014· Flawless Beauty LLC

Recalled Item: Relumins Advanced Glutathione (lyophilized glutathione/vitamin C) injectable...

The Issue: Marketed Without An Approved NDA/ANDA: Product is sold over the counter...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 29, 2014· Flawless Beauty LLC

Recalled Item: Laroscorbine Platinium (vitamin C/collagen) injectable I.V. solution...

The Issue: Marketed Without An Approved NDA/ANDA: Product is sold over the counter...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 29, 2014· Flawless Beauty LLC

Recalled Item: Saluta (reduced glutathione) Powder for Injection Recalled by Flawless...

The Issue: Marketed Without An Approved NDA/ANDA: Parenteral product is labeled for use...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 29, 2014· Flawless Beauty LLC

Recalled Item: Vitamin C (ascorbic acid) Injection Recalled by Flawless Beauty LLC Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Parenteral product is sold over the...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 29, 2014· Mercola Group

Recalled Item: Organic Cocoa Cassava bars Recalled by Mercola Group Due to Undeclared Milk

The Issue: This voluntary recall has been initiated because the Dr. Mercola Organic...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 29, 2014· Childrens Medical Ventures

Recalled Item: Philips/Children's Medical Ventures Smart Monitor 2 Professional Series...

The Issue: The battery pack wire harness is improperly assembled rendering the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2014· Convatec Inc.

Recalled Item: Convatec Flexi Seal Control Fecal Management System Rx Only by Convatec Inc....

The Issue: Convatec Inc. is recalling Flexi-seal FMS Control Kit since it does not have...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 29, 2014· Synthes, Inc.

Recalled Item: Synthes ProDisc-C 2.0mm Milling Bit Recalled by Synthes, Inc. Due to Certain...

The Issue: Certain lots of the ProDisc-C 2.0mm Milling Bits have an increased potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2014· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Connection issues between the PD transfer set catheter connector and an...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2014· Atrium Medical Corporation

Recalled Item: Atrium Express Dry Seal Chest Drain ATS Blood Recovery Recalled by Atrium...

The Issue: Product that was previously recalled because the Chest Drain tubing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2014· Greatbatch Medical

Recalled Item: Coaxial Micro-Introducer Kit. Greatbatch Part Number/Bard Access Systems...

The Issue: Greatbatch identified that the documentation does not support the five-year...

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

Class II — Potential Health HazardOngoing
DrugApril 25, 2014· Prestige Brands Holdings

Recalled Item: PediaCare brand NIGHTTIME MULTI-SYMPTOM Cold Recalled by Prestige Brands...

The Issue: Presence of Precipitate; small amounts of diphenhydramine precipitated out...

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

Class III — Low RiskOngoing
Refund
DrugApril 25, 2014· Prestige Brands Holdings

Recalled Item: PediaCare brand DAY & NIGHT Value Pack DAYTIME MULTI-SYMPTOM Cold Recalled...

The Issue: Presence of Precipitate; small amounts of diphenhydramine precipitated out...

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

Class III — Low RiskOngoing
Refund
FoodApril 25, 2014· Kroger Co

Recalled Item: Private Selection Chocolate Hazelnut Mascarpone Ice Cream Recalled by Kroger...

The Issue: The firm discovered that the label for two of their products did not declare...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 25, 2014· Kroger Co

Recalled Item: Private Selection Caramel Hazelnut Fudge Truffle Ice Cream Recalled by...

The Issue: The firm discovered that the label for two of their products did not declare...

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

Class I — Serious Health HazardOngoing
Refund