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. 1,818 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
1,818 in last 12 months

Showing 4178141800 of 49,677 recalls

Medical DeviceJune 23, 2014· Cordis Corporation

Recalled Item: Cordis EMPIRA NC RX PTCA Dilatation Catheter Recalled by Cordis Corporation...

The Issue: The balloon may exhibit resistance to the removal of the balloon cover....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: SIEMENS ADVIA Centaur CP Immunoassay System BNP kit Recalled by Siemens...

The Issue: Complaints of failed calibration.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: SIEMENS ADVIA Centaur CP Immunoassay System BNP kit Recalled by Siemens...

The Issue: Complaints of failed calibration.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2014· Stryker Endoscopy

Recalled Item: Disposable StrykeFlow Tip Recalled by Stryker Endoscopy Due to Internal...

The Issue: Internal review found that six lots of Disposable StrykeFlow Tips were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2014· Laser Peripherals LLC

Recalled Item: LP Recalled by Laser Peripherals LLC Due to Mislabeling

The Issue: Laser Peripherals LLC is recalling DBLF-60-2 Bare Laser due to a mislabeling...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2014· ORIGIO, Inc

Recalled Item: Name: Pasteur Pipets Recalled by ORIGIO, Inc Due to Identification of...

The Issue: Identification of packaging breach of the nylon pouch sterile barrier for...

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

Class II — Potential Health HazardOngoing
DrugJune 20, 2014· Mylan Pharmaceuticals Inc.

Recalled Item: Tolterodine Tartrate Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications; Out of specification for...

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

Class III — Low RiskOngoing
Refund
DrugJune 20, 2014· Novel Laboratories, Inc.

Recalled Item: Famotidine for Oral Suspension Recalled by Novel Laboratories, Inc. Due to...

The Issue: Failed Impurity/Degradation Specification; 12-month stability time point

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

Class III — Low RiskOngoing
Refund
DrugJune 19, 2014· Mckesson Packaging Services

Recalled Item: Aspirin DR Enteric Coated Tablets Recalled by Mckesson Packaging Services...

The Issue: Failed Dissolution Specification; at the 12 month time interval.

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

Class III — Low RiskOngoing
Refund
DrugJune 19, 2014· Mylan Pharmaceuticals Inc.

Recalled Item: Diltiazem HCl Extended Release Capsules Recalled by Mylan Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...

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

Class III — Low RiskOngoing
Refund
DrugJune 19, 2014· Pfizer Inc.

Recalled Item: Cardura XL (doxazosin mesylate extended release tablets Recalled by Pfizer...

The Issue: Failed Impurities/Degradation Specifications: Product from this lot may not...

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

Class III — Low RiskOngoing
Refund
DrugJune 19, 2014· Forest Pharmaceuticals Inc

Recalled Item: Bystolic (nebivolol) tablets Recalled by Forest Pharmaceuticals Inc Due to...

The Issue: Failed Dissolution Specifications: Drug failed stage III dissolution testing.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 19, 2014· Abbott Molecular

Recalled Item: 5 mL Reaction Vessels (a consumable of the Abbott m2000sp Recalled by Abbott...

The Issue: Abbott Molecular identified that some of the 5 ml Reaction Vessels (RVs)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2014· Boston Scientific CRM Corp

Recalled Item: Boston Scientific ENDOTAK RELIANCE¿ SG Recalled by Boston Scientific CRM...

The Issue: A review of manufacturing test records for Boston Scientific ENDOTAK...

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

Class II — Potential Health HazardOngoing
FoodJune 19, 2014· Country Life

Recalled Item: Country Life TARGET MINS CALCIUM MAGNESIUM With Vitamin D3 Complex Recalled...

The Issue: The affected lots do not meet quality standards due to insoluble particulates.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 17, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Syngo RT Therapist and Syngo RT Oncologist intended use Recalled by...

The Issue: Siemens became aware of a potential issue with the syngo RT Therapist...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo¿ Advanced Perfusion System 1 100/120V AC Recalled by Terumo...

The Issue: An evaluation of the APS1 Operator Manual found that existing instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2014· Varian Medical Systems, Inc.

Recalled Item: C-Series High Energy Linear Accelerator - Models: Novalis Tx Recalled by...

The Issue: Trend in reports of unexpected decrease in beam output in C-series High...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2014· Baxter Healthcare Corp.

Recalled Item: Baxter MiniCap with Povidone-Iodine Solution Recalled by Baxter Healthcare...

The Issue: Inadequate iodine and packaging related defects.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo¿ Advanced Perfusion System 1 220/240V AC Recalled by Terumo...

The Issue: An evaluation of the APS1 Operator Manual found that existing instructions...

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

Class II — Potential Health HazardOngoing