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. 1,070 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
1,070 in last 12 months

Showing 15861–15880 of 49,677 recalls

FoodApril 12, 2021· NATURE'S SUNSHINE PRODUCTS

Recalled Item: Love & Peas Protein Rich Meal Replacement Recalled by NATURE'S SUNSHINE...

The Issue: The firm was notified by its ingredient supplier of Medium Chain...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 12, 2021· NATURE'S SUNSHINE PRODUCTS

Recalled Item: Love & Peas Protein Rich Meal Replacement Recalled by NATURE'S SUNSHINE...

The Issue: The firm was notified by an ingredient supplier of Medium Chain...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 10, 2021· HOSTESS BRANDS LLC

Recalled Item: Hostesss SnoBalls packaged as Hostess Chocolate CupCakes Recalled by HOSTESS...

The Issue: SnoBalls snack cakes were packaged with a label for Chocolate CupCakes...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 9, 2021· Teligent Pharma, Inc.

Recalled Item: Flurandrenolide Ointment USP Recalled by Teligent Pharma, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications:

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 9, 2021· Avid Medical, Inc.

Recalled Item: FISTULA (ON/OFF) ALL IN ONE BAG. Medical convenience kit Recalled by Avid...

The Issue: Medical convenience kits are being recalled due to a potential breach in the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 9, 2021· Medical Action Industries, Inc. 306

Recalled Item: Kit: Blood Culture. MAI Kit Part Number: 80315D Recalled by Medical Action...

The Issue: Medical convenience kits are being recalled due to a potential breach in the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 9, 2021· Medical Action Industries, Inc. 306

Recalled Item: Kit: LVAD Dres Chg. MAI Kit Part Number: 79544B Recalled by Medical Action...

The Issue: Medical convenience kits are being recalled due to a potential breach in the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 9, 2021· INNOVA MEDICAL GROUP, INC.

Recalled Item: COVID-19 Self-Test Kit *** INNOVA *** 7T Recalled by INNOVA MEDICAL GROUP,...

The Issue: Due to distributing test kits to customers who were not part of a clinical...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 9, 2021· SPINEART SA

Recalled Item: PERLA TL Lateral Connector Open - Product Usage: intended to Recalled by...

The Issue: Due to external labelling error/mix-up. Affected product external labels...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2021· Avid Medical, Inc.

Recalled Item: FISTULA ON-OFF KIT. Medical convenience kit Recalled by Avid Medical, Inc....

The Issue: Medical convenience kits are being recalled due to a potential breach in the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 9, 2021· Medical Action Industries, Inc. 306

Recalled Item: Kit: Midline Insertion DA. MAI Kit Part Number: 77981B Recalled by Medical...

The Issue: Medical convenience kits are being recalled due to a potential breach in the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 9, 2021· Medical Action Industries, Inc. 306

Recalled Item: Kit: Blood Culture MAI Kit Part Number: 80076 Recalled by Medical Action...

The Issue: Medical convenience kits are being recalled due to a potential breach in the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 9, 2021· Avid Medical, Inc.

Recalled Item: ADULT CHEST TUBE TRAY. Medical convenience kit Recalled by Avid Medical,...

The Issue: Medical convenience kits are being recalled due to a potential breach in the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 9, 2021· INNOVA MEDICAL GROUP, INC.

Recalled Item: For In Vitro Diagnostic Use Only *** 25T 888 SARS-CoV-2 Recalled by INNOVA...

The Issue: Due to distributing test kits to customers who were not part of a clinical...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 9, 2021· Medical Action Industries, Inc. 306

Recalled Item: Kit: CentralLineDresChangeClrSeq MAI Kit Part Number: 79420 Recalled by...

The Issue: Medical convenience kits are being recalled due to a potential breach in the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 9, 2021· Medical Action Industries, Inc. 306

Recalled Item: Kit: Injection REVIEW MAI Kit Part Number: 74736 Recalled by Medical Action...

The Issue: Medical convenience kits are being recalled due to a potential breach in the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 9, 2021· INNOVA MEDICAL GROUP, INC.

Recalled Item: COVID-19 Self-Test Kit *** INNOVA *** 3T Recalled by INNOVA MEDICAL GROUP,...

The Issue: Due to distributing test kits to customers who were not part of a clinical...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 9, 2021· Avid Medical, Inc.

Recalled Item: DIALYSIS ACCESS Medical convenience kit Recalled by Avid Medical, Inc. Due...

The Issue: Medical convenience kits are being recalled due to a potential breach in the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 8, 2021· Meridian Bioscience Inc

Recalled Item: Revogene RNA Software Upgrade Kit Revogene RNA Software Upgrade USBs...

The Issue: Emergency Use Application (EUA) application withdrawn as false negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2021· Smith & Nephew, Inc.

Recalled Item: CANNU-Flex SILK Interference Screws 6 mmx 30 mm - Product Recalled by Smith...

The Issue: Mislabeled box contained a 6mm x 20mm screw instead of 6mm x 30mm screw

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

Class II — Potential Health HazardOngoing