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. 1,744 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
1,744 in last 12 months

Showing 4826148280 of 49,677 recalls

DrugJuly 25, 2012· Lloyd Inc. of Iowa

Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...

The Issue: Subpotent; 9-month stability interval

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 25, 2012· Lloyd Inc. of Iowa

Recalled Item: Thyro-Tab 0.050 mg. Recalled by Lloyd Inc. of Iowa Due to Subpotent; 9-month...

The Issue: Subpotent; 9-month stability interval

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 25, 2012· Lloyd Inc. of Iowa

Recalled Item: Thyro-Tab 0.075 mg. Recalled by Lloyd Inc. of Iowa Due to Subpotent; 9-month...

The Issue: Subpotent; 9-month stability interval

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 25, 2012· American Health Packaging

Recalled Item: Topiramate Tablets Recalled by American Health Packaging Due to Labeling:...

The Issue: Labeling: Label Mix-Up: A typographical error in the product form on the...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 25, 2012· Aesculap Implant Systems LLC

Recalled Item: Aesculap S4 Element 4.5mm Polyaxial Screws (ST240T Recalled by Aesculap...

The Issue: There is a possibility that the screw channel that holds the rod in place...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur Multi-Diluent 1 - Used for automated dilutions...

The Issue: Decrease in onboard dilution recovery when using Multi-Diluent 1 that has...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2012· Beckman Coulter Inc.

Recalled Item: Access Folate WHO Calibrators Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter is recalling the Access Folate Calibrators because it may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2012· Capintec Inc

Recalled Item: Capintec Captus 3000 Thyroid Uptake System Nuclear uptake probe intended...

The Issue: Customers who received a Capintec Captus 3000 Thyroid Uptake System with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine EXPEDIUM Offset Torque Wrench Product Code 2797-29-510 The...

The Issue: A component within the handle of the Expedium Offset Torque Wrench is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2012· Beckman Coulter Inc.

Recalled Item: Access Folate Calibrators Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is recalling the Access Folate Calibrators because it may...

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

Class II — Potential Health HazardOngoing
DrugJuly 24, 2012· Cadence Pharmaceuticals

Recalled Item: OFIRMEV (acetaminophen) injection Recalled by Cadence Pharmaceuticals Due to...

The Issue: Presence of Particulate Matter: The firm initiated the recall due to visible...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 23, 2012· Stat Rx USA

Recalled Item: Tizanidine (Generic for: Zanaflex) Recalled by Stat Rx USA Due to Labeling:...

The Issue: Labeling: Label Mix-Up; Some bottles of Tizanidine 4mg Tablets, had the...

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

Class III — Low RiskOngoing
Refund
DrugJuly 23, 2012· American Health Packaging

Recalled Item: Mercaptopurine Tablets Recalled by American Health Packaging Due to Failed...

The Issue: Failed USP Dissolution Test Requirements: This sub-recall is in response to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 23, 2012· Cisco Systems Inc

Recalled Item: Cisco brand HealthPresence Recalled by Cisco Systems Inc Due to Software...

The Issue: Software anomaly may result in incorrect values and interpretations. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2012· Teleflex Medical

Recalled Item: TAUT Recalled by Teleflex Medical Due to Product is missing the label on the...

The Issue: Product is missing the label on the internal packaging.

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

Class III — Low RiskOngoing
Medical DeviceJuly 20, 2012· Galil Medical, Inc.

Recalled Item: Visual-ICE¿ Cryoablation System Recalled by Galil Medical, Inc. Due to Galil...

The Issue: Galil Medical is recalling a number of Visual Ice Cryoablation Systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2012· GE Healthcare, LLC

Recalled Item: CARESCAPE Monitor B850 Product Usage: The CARESCAPE TM Monitor B850 Recalled...

The Issue: GE Healthcare become aware of 4 potential issues associated with the...

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

Class II — Potential Health HazardOngoing
FoodJuly 20, 2012· Sartori Inspirations, LLC

Recalled Item: Smoked Gouda packaged in 7 oz clear plastic containers Recalled by Sartori...

The Issue: Sartori is recalling various dips, salsas, and cheese products which may...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 20, 2012· Sartori Inspirations, LLC

Recalled Item: Jalapeno Pimento Cheese packaged in 7 oz clear plastic containers Recalled...

The Issue: Sartori is recalling various dips, salsas, and cheese products which may...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 20, 2012· Sartori Inspirations, LLC

Recalled Item: Famous Thick Salsa packaged in 7 oz clear plastic containers Recalled by...

The Issue: Sartori is recalling various dips, salsas, and cheese products which may...

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

Class II — Potential Health HazardOngoing
Refund