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. 2,450 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,450 in last 12 months

Showing 3116131180 of 49,677 recalls

Medical DeviceJanuary 19, 2017· Applied Medical Technology Inc

Recalled Item: AMT Bridle - Nasal Tube Retaining System Used with...

The Issue: Expired expiration dates are listed on the pouches.

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

Class III — Low RiskOngoing
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Potassium Chloride Oral Solution Recalled by VistaPharm, Inc. Due to...

The Issue: Defective Container: Leakage of unit dose cups that may occur at the seal.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Metoclopramide Oral Solution Recalled by VistaPharm, Inc. Due to CGMP...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Lactulose Solution Recalled by VistaPharm, Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Lactulose Solution Recalled by VistaPharm, Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Nystatin Oral Suspension Recalled by VistaPharm, Inc. Due to CGMP...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Oral Solution Recalled by...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Methadone Hydrochloride Oral Concentrate Recalled by VistaPharm, Inc. Due to...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Phenytoin Oral Suspension Recalled by VistaPharm, Inc. Due to CGMP...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Oxycodone Hydrochloride Oral Solution Recalled by VistaPharm, Inc. Due to...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Methadone Hydrochloride Oral Concentrate Recalled by VistaPharm, Inc. Due to...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Methadone Hydrochloride Oral Concentrate Recalled by VistaPharm, Inc. Due to...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Nystatin Oral Suspension Recalled by VistaPharm, Inc. Due to CGMP...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 18, 2017· D. F. Stauffer Biscuit Co, Inc.

Recalled Item: FRONT: Stauffer's Animal Crackers Original Recalled by D. F. Stauffer...

The Issue: D. F. Stauffer Biscuit Co., Inc. is voluntarily recalling one specific best...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 18, 2017· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Brilliance iCT X-Ray Recalled by Philips Electronics...

The Issue: During a bolus tracking procedure, no images were generated when the scan...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2017· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity CT X-Ray Recalled by Philips Electronics North...

The Issue: During a bolus tracking procedure, no images were generated when the scan...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2017· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity Core128 X-Ray Recalled by Philips Electronics...

The Issue: During a bolus tracking procedure, no images were generated when the scan...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2017· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity Core X-Ray Recalled by Philips Electronics...

The Issue: During a bolus tracking procedure, no images were generated when the scan...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2017· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Brilliance 64 System Recalled by Philips Electronics...

The Issue: During a bolus tracking procedure, no images were generated when the scan...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2017· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Brilliance iCT SP X-Ray Recalled by Philips Electronics...

The Issue: During a bolus tracking procedure, no images were generated when the scan...

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

Class II — Potential Health HazardOngoing