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. 2,413 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,413 in last 12 months

Showing 3888138900 of 49,677 recalls

DrugMarch 25, 2015· Heritage Pharmaceuticals, Inc.

Recalled Item: GLIPIZIDE and METFORMIN HYDROCHLORIDE Tablets Recalled by Heritage...

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

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 25, 2015· Nidek Inc

Recalled Item: Endophotocoagulation Delivery 4EP-1 of GYC-1000 Green Laser Photocoagulator...

The Issue: Accessories to the GYC-1000 laser were missing Laser Aperture labels.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2015· Nidek Inc

Recalled Item: Dual Delivery 4DD-1 of GYC-1000 Green Laser Photocoagulator system GYC4DD-1:...

The Issue: Accessories to the GYC-1000 laser were missing Laser Aperture labels.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Universal Charger Product Usage: The Stryker Universal Battery Charger is...

The Issue: The Stryker Universal Battery Charger is not transmitting usage data to the...

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

Class III — Low RiskOngoing
Medical DeviceMarch 25, 2015· Lumenis Limited

Recalled Item: Light Sheer Desire Diode Laser System with XC Handpiece Accessory options....

The Issue: Device software treatment preset parameters for the XC treatment handpiece...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2015· Laax, Inc.

Recalled Item: TIGERPAW System II Recalled by Laax, Inc. Due to Increase of field reports...

The Issue: Increase of field reports involving issues with the TIGERPAW System II...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 25, 2015· Laax, Inc.

Recalled Item: TIGERPAW System II Recalled by Laax, Inc. Due to Increase of field reports...

The Issue: Increase of field reports involving issues with the TIGERPAW System II...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 25, 2015· CSA Medical

Recalled Item: CSA Medical truFreeze Console- Cryosurgical Unit Cryogenic Surgical Device...

The Issue: TruFreeze Console caused a higher rate of liquid nitrogen (cryogen) to be...

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

Class II — Potential Health HazardOngoing
DrugMarch 24, 2015· Nomax Inc

Recalled Item: Rose Bengal GloStrips (rose bengal) Ophthalmic Strips USP Recalled by Nomax...

The Issue: Failed Content Uniformity Specifications: The product may not meet finished...

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

Class III — Low RiskOngoing
Refund
DrugMarch 24, 2015· Nomax Inc

Recalled Item: Fluorescein Sodium Ophthalmic Strips USP Recalled by Nomax Inc Due to Failed...

The Issue: Failed Content Uniformity Specifications: The product may not meet finished...

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

Class III — Low RiskOngoing
Refund
DrugMarch 24, 2015· Nomax Inc

Recalled Item: Fluorescein Sodium Ophthalmic Strips USP Recalled by Nomax Inc Due to Failed...

The Issue: Failed Content Uniformity Specifications: The product may not meet finished...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 24, 2015· Hamilton Medical, Inc.

Recalled Item: Hamilton-G5 Ventilators with software versions V2.40/2.41 Catalog numbers...

The Issue: Customer reports that the ventilator display can freeze. Ventilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2015· The Anspach Effort, Inc.

Recalled Item: Synthes Small Battery Drive (SBD) Oscillating Saw Attachment Part Number:...

The Issue: The potential exists for the Oscillating Saw Attachment to disengage from...

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

Class II — Potential Health HazardOngoing
DrugMarch 23, 2015· Mylan Institutional LLC

Recalled Item: Gemcitabine for Injection Recalled by Mylan Institutional LLC Due to...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 23, 2015· Mylan Institutional LLC

Recalled Item: Gemcitabine for Injection Recalled by Mylan Institutional LLC Due to...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 23, 2015· Mylan Institutional LLC

Recalled Item: Gemcitabine for Injection Recalled by Mylan Institutional LLC Due to...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 23, 2015· Baxter Healthcare Corp

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp Due to...

The Issue: Lack of Assurance of Sterility; increased complaints received for leaks

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2015· Baxter Healthcare Corp

Recalled Item: Clinimix E 5/20 sulfite-free (5% amino-acid with electrolytes in 20%...

The Issue: Lack of Assurance of Sterility; increased complaints received for leaks

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 23, 2015· Superior Foods

Recalled Item: Simply Balanced Organic Chopped Spinach NET WT 10 OZ (283g) Recalled by...

The Issue: Possible Listeria contamination

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 23, 2015· Carmel Food Group, Inc.

Recalled Item: Rising Moon Organics Spinach Florentine Ravioli Recalled by Carmel Food...

The Issue: Firm was notified by supplier of spinach and used in manufacturing showed...

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

Class II — Potential Health HazardOngoing
Refund