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. 2,627 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,627 in last 12 months

Showing 72017220 of 13,417 recalls

DrugApril 27, 2018· Sanofi-Aventis U.S. LLC

Recalled Item: Docetaxel injection concentrate Recalled by Sanofi-Aventis U.S. LLC Due to...

The Issue: Superpotent drug: over-concentrated vials of Docetaxel injection concentrate...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2018· Sun Pharmaceutical Industries, Inc.

Recalled Item: Riomet (metformin hydrochloride oral solution) Recalled by Sun...

The Issue: Labeling: Not Elsewhere Classified: Sun Pharma has decided to initiate this...

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

Class III — Low RiskOngoing
Refund
DrugApril 23, 2018· Mckesson Packaging Services

Recalled Item: Diltiazem CD (Diltiazem Hydrochloride Extended-Release Capsules Recalled by...

The Issue: Failed Dissolution Specifications. High dissolution results were obtained...

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

Class III — Low RiskOngoing
Refund
DrugApril 23, 2018· Mckesson Packaging Services

Recalled Item: Diltiazem HCl Extended-Release Capsules Recalled by Mckesson Packaging...

The Issue: Failed Dissolution Specifications. High dissolution results were obtained...

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

Class III — Low RiskOngoing
Refund
DrugApril 23, 2018· Mckesson Packaging Services

Recalled Item: Diltiazem HCl Extended-Release Capsules Recalled by Mckesson Packaging...

The Issue: Failed Dissolution Specifications. High dissolution results were obtained...

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

Class III — Low RiskOngoing
Refund
DrugApril 23, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Dr. Reddy's...

The Issue: Presence of Foreign Tablets/Capsules: One foreign tablet identified as...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2018· Exela Pharma Sciences LLC

Recalled Item: Diclofenac Sodium and Misoprostol Delayed Release Tablets 75 mg/0.2 mg...

The Issue: Labeling: Label Mix-Up: bottle labeled as Diclofenac Sodium and Misoprostol...

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

Class II — Potential Health HazardOngoing
Refund
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
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
DrugApril 16, 2018· Epic Products, LLC

Recalled Item: Euphoric Premium Male Performance Enhancer capsules Recalled by Epic...

The Issue: Marketed Without An Approved NDA/ANDA: product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2018· Boiron Inc.

Recalled Item: Calendula Cream Recalled by Boiron Inc. Due to Labeling: Labeling Error on...

The Issue: Labeling: Labeling Error on Declared Strength; The outer carton (secondary...

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

Class III — Low RiskOngoing
Refund
DrugApril 12, 2018· AMA Wholesale

Recalled Item: Rhino 69 Extreme 50000 packaged in 1 capsule per blister pack Recalled by...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 11, 2018· Premier Pharmacy Labs Inc

Recalled Item: Morphine Sulfate 4 mg/mL PF Injection. 1 mL in a Recalled by Premier...

The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 11, 2018· Premier Pharmacy Labs Inc

Recalled Item: NEOstigmine Methylsulfate (1 mg/mL) 3mg per 3mL. 3mL Single Dose Recalled by...

The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 11, 2018· Premier Pharmacy Labs Inc

Recalled Item: Hydromorphone HCl 1 mg/mL PF INJ. 1mL in a 3mL Recalled by Premier Pharmacy...

The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 11, 2018· Premier Pharmacy Labs Inc

Recalled Item: Morphine Sulfate 2 mg/mL PF Injection. 1 mL in a Recalled by Premier...

The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 10, 2018· Pharmalucence, Inc.

Recalled Item: Kit for the Preparation of Technetium TC-99M Mebrofenin Recalled by...

The Issue: Failed Stability Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 9, 2018· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours...

The Issue: Defective Delivery System: Out of specification for adhesive transfer.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 6, 2018· Sandoz Incorporated

Recalled Item: Triamterene and Hydrochlorothiazide Tablets Recalled by Sandoz Incorporated...

The Issue: Cross Contamination With Other Products: presence of unrelated ingredients...

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

Class III — Low RiskOngoing
Refund
DrugApril 5, 2018· Coastal Meds, LLC.

Recalled Item: LIPO-B Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr. Recalled...

The Issue: Presence of Particulate matter. Recall due to presence of unknown...

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

Class II — Potential Health HazardOngoing
Refund