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. 2,453 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,453 in last 12 months

Showing 2716127180 of 49,677 recalls

Medical DeviceJanuary 19, 2018· Mako Surgical Corporation

Recalled Item: Restoris MCK Onlay Insert Extractor. Recalled by Mako Surgical Corporation...

The Issue: Possible hinge pin disassociation from the Mako Onlay Insert Extractor.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2018· Beckman Coulter Inc.

Recalled Item: AutoMate 2550 "High Speed" Catalog Number ODL25255 Recalled by Beckman...

The Issue: A misaligned pipette tip sensor poses the remote risk of cross-contamination...

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

Class II — Potential Health HazardOngoing
DrugJanuary 17, 2018· Magno Humphries Laboratories, Inc

Recalled Item: Senna Laxative (sennosides) tablets Recalled by Magno Humphries...

The Issue: Labeling: Label Mix-Up: Customer complaint received that a bottle labeled as...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 17, 2018· CHOBANI

Recalled Item: Chobani Flip Key Lime Crumble - Key Lime Low-Fat Greek Recalled by CHOBANI...

The Issue: Product is recalled because a statement on the overwrap label erroneously...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 17, 2018· Olympus Corporation of the Americas

Recalled Item: Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R Recalled by...

The Issue: Potential breakage of the endoscope s insertion tube bending section during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2018· Olympus Corporation of the Americas

Recalled Item: Uretero-reno fiberscope URF-P6RP6 Recalled by Olympus Corporation of the...

The Issue: Breakage of the endoscope's insertion tube bending section during surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2018· Olympus Corporation of the Americas

Recalled Item: Uretero-reno fiberscope URF-P6 Recalled by Olympus Corporation of the...

The Issue: Breakage of the endoscope's insertion tube bending section during surgical...

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

Class II — Potential Health HazardOngoing
DrugJanuary 16, 2018· Fresenius Kabi USA, LLC

Recalled Item: Vecuronium bromide for Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Failed impurities/ degradation specifications: Out-of-specification (OOS)...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 16, 2018· Sun Pharmaceutical Industries, Inc.

Recalled Item: DOXOrubicin Hydrochloride Liposome Injection Recalled by Sun Pharmaceutical...

The Issue: Lack Of Assurance Of Sterility

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 16, 2018· Ottogi America Inc

Recalled Item: Ottogi Rice Cake Soup Recalled by Ottogi America Inc Due to Undeclared Milk

The Issue: Firm determined that their Rice Cake Soup has undeclared milk in the form of...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2018· Jarrow Formulas Inc

Recalled Item: Jarrow Formulas Liquid L-Carnitine Recalled by Jarrow Formulas Inc Due to A...

The Issue: A higher than normal micro result was found at the six month time point for...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 12, 2018· AuroMedics Pharma LLC

Recalled Item: Levofloxacin in 5% Dextrose Injection Recalled by AuroMedics Pharma LLC Due...

The Issue: Presence of Particulate Matter; contains visible particulate matter...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 12, 2018· International Laboratories, Inc.

Recalled Item: Pravastatin Sodium Tablets Recalled by International Laboratories, Inc. Due...

The Issue: Presence of Foreign Tablets/Capsules: bottles could contain both pravastatin...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 12, 2018· International Laboratories, Inc.

Recalled Item: Pravastatin Sodium Tablets Recalled by International Laboratories, Inc. Due...

The Issue: Presence of Foreign Tablets/Capsules: bottles could contain both pravastatin...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 12, 2018· Manicaretti Inc

Recalled Item: IASA COLATURA DI ALICI DI CETARA ANCHOVY EXTRACT Recalled by Manicaretti Inc...

The Issue: Rapid Alert System for Food and Feed notification received from Italy...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 12, 2018· Beckman Coulter Inc.

Recalled Item: 1) Cytomics FC 500 With CXP Software BECKMAN COULTER 2) Recalled by Beckman...

The Issue: A manufacturing defect on the amplifier board of the Flow Cytometers my...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 12, 2018· Beckman Coulter Inc.

Recalled Item: COULTER EPICS XL Flow Cytometer COULTER EPICS XL-MCL Flow Cytometer Recalled...

The Issue: A manufacturing defect on the amplifier board of the Flow Cytometers my...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 12, 2018· Tecan US, Inc.

Recalled Item: Cortisol Saliva Luminescence Immunoassay The IBL International Cortisol...

The Issue: Product is not meeting specification for traceability to NIST cortisol...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2018· Medline Industries, Inc.

Recalled Item: BARD MYPICC Kit Recalled by Medline Industries, Inc. Due to One of the cases...

The Issue: One of the cases of product might not have been sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2018· Shimadzu Medical Systems

Recalled Item: Sonialvision Safire II Recalled by Shimadzu Medical Systems Due to When...

The Issue: When selecting serial radiography with a pulse rate of 7.5fps (including...

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

Class II — Potential Health HazardOngoing