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 2606126080 of 49,677 recalls

Medical DeviceMay 18, 2018· Qiagen Sciences, Inc.

Recalled Item: AmniSure ROM Test under the following labels: 1) Catalog Number Recalled by...

The Issue: Potential for control line not appearing on the test strip

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 18, 2018· OMNIlife science Inc.

Recalled Item: OMNI Hip System Recalled by OMNIlife science Inc. Due to The Internal...

The Issue: The Internal packaging, the pouch and patient labels are improperly labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2018· BERLIN HEART GMBH

Recalled Item: EXCOR Pediatric Ventricular Assist Device Blood Pumps Recalled by BERLIN...

The Issue: There is a potential for a disruption in one or more of the triple layer...

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

Class I — Serious Health HazardOngoing
FoodMay 17, 2018· Ziyad Brothers Importing, Inc.

Recalled Item: Ziyad Brand Tahini Recalled by Ziyad Brothers Importing, Inc. Due to...

The Issue: Ziyad Brothers Importing is voluntarily recalling its Ziyad Brand Tahini, 8...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 17, 2018· Arrow International Inc

Recalled Item: VPS Rhythm ECG Accessory Pack Recalled by Arrow International Inc Due to...

The Issue: Product pouch label may not easily identify the lot number, expiration date...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2018· Arrow International Inc

Recalled Item: Peripherally Inserted Midline Catheter Kit with Placement Wire Recalled by...

The Issue: Product pouch label may not easily identify the lot number, expiration date...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2018· Arrow International Inc

Recalled Item: VPS TipTracker Stylet Accessory Recalled by Arrow International Inc Due to...

The Issue: Product pouch label may not easily identify the lot number, expiration date...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2018· Arrow International Inc

Recalled Item: VPS Rhythm ECG Accessory Pack with Johans Adapter Recalled by Arrow...

The Issue: Product pouch label may not easily identify the lot number, expiration date...

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

Class II — Potential Health HazardOngoing
DrugMay 17, 2018· Shoreside Enterprises Inc.

Recalled Item: POSEIDON Xtreme PLATINUM 4500 Recalled by Shoreside Enterprises Inc. Due to...

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

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 17, 2018· Lupin Pharmaceuticals Inc.

Recalled Item: My Way (Levonorgestrel) Tablets TWO PACK Recalled by Lupin Pharmaceuticals...

The Issue: Marketed Without an Approved NDA/ANDA: 2-pack configuration did not receive...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 17, 2018· Shoreside Enterprises Inc.

Recalled Item: 7K capsules packaged in single packs sold in 24-count boxes Recalled by...

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

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 17, 2018· Lupin Pharmaceuticals Inc.

Recalled Item: My Way (levonorgestrel) Tablets TWO PACK Recalled by Lupin Pharmaceuticals...

The Issue: Marketed Without an Approved NDA/ANDA: 2-pack configuration did not receive...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 16, 2018· Ideaz Llc

Recalled Item: screamin' menthol (menthol) Pain Relieving Gel Recalled by Ideaz Llc Due to...

The Issue: CGMP Deviations: Products manufactured with an ingredient that exceed the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 16, 2018· Inopak Ltd

Recalled Item: Option Systems Antibacterial Foaming Hand Wash with .3% PCMX Recalled by...

The Issue: Microbial contamination of NonSterile Product; FDA analysis returned out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 16, 2018· Ideaz Llc

Recalled Item: screamin' hot (capsaicin) Pain Relieving Gel Recalled by Ideaz Llc Due to...

The Issue: CGMP Deviations: Products manufactured with an ingredient that exceed the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: Immunoglobulin A is an in vitro diagnostic assay for the Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: C4 is an in vitro diagnostic assay for the quantitative Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: The Recalled by Abbott Laboratories, Inc Due to An update to the Reagents...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: C3 is an in vitro diagnostic assay for the quantitative Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: Transferrin is an in vitro diagnostic assay for the quantitative Recalled by...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing