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 2842128440 of 49,677 recalls

Medical DeviceJuly 28, 2017· C.R. Bard, Inc.

Recalled Item: Bard Magic 3 Antibacterial Hydrophilic Intermittent Catheter Female Recalled...

The Issue: Specific lots labeled as an Antibacterial Hydrophilic Intermittent Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2017· Cardinal Health 200, LLC

Recalled Item: Convertors Robotic Drape with Attached Leggings Recalled by Cardinal Health...

The Issue: Product 29474 LAVH drape was packaged as 29574 Robotic Drape with Leggings.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2017· Zimmer Surgical Inc

Recalled Item: A.T.S. 2200TS Tourniquet Systems Recalled by Zimmer Surgical Inc Due to...

The Issue: Updated on-device label and 3 pages of an updated Operator/Service Manual....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2017· Zimmer Surgical Inc

Recalled Item: A.T.S. 4000TS Tourniquet Systems Recalled by Zimmer Surgical Inc Due to...

The Issue: Updated on-device label and 3 pages of an updated Operator/Service Manual....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2017· Medtronic Navigation, Inc.

Recalled Item: VCLAS (Visualase Cooled Laser Ablation System) Part Number: 9735559...

The Issue: The VCLAS 3mm, 10mm, and 15mm tip devices were not appropriately tested for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2017· Optovue, Inc.

Recalled Item: iFusion Recalled by Optovue, Inc. Due to FDA determined that a 510(k) is...

The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2017· Optovue, Inc.

Recalled Item: iVue with Normative Database Recalled by Optovue, Inc. Due to FDA determined...

The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2017· Optovue, Inc.

Recalled Item: iVue 500 with iScan Recalled by Optovue, Inc. Due to FDA determined that a...

The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...

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

Class II — Potential Health HazardOngoing
DrugJuly 26, 2017· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Presence...

The Issue: Presence of Particulate Matter; stainless steel

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2017· HOSPIRA INC, LAKE FOREST

Recalled Item: Hydromorphone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST...

The Issue: Presence of Particulate Matter: Silicone oil

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2017· HOSPIRA INC, LAKE FOREST

Recalled Item: Hydromorphone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST...

The Issue: Presence of Particulate Matter: Silicone oil

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2017· HOSPIRA INC, LAKE FOREST

Recalled Item: Hydromorphone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST...

The Issue: Presence of Particulate Matter: Silicone oil

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Acidophilus-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared...

The Issue: Undeclared allergens: milk (Colostrum, Dried Yogurt, Whey).

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Leci-thin-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared...

The Issue: Undeclared allergens: soy (lecithin)

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Heart-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens

The Issue: Undeclared allergens: soy (lecithin)

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Pancreas-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens

The Issue: Undeclared allergens: soy (lecithin)

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Thymus Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens

The Issue: Undeclared allergens: milk (Colostrum)

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Liver-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens

The Issue: Undeclared allergens: soy (lecithin)

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Metabo-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens

The Issue: Undeclared allergens: milk (Whey)

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 26, 2017· NatureAll-STF Holding, LLC

Recalled Item: Prostate-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens

The Issue: Undeclared allergens: soy (lecithin)

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

Class II — Potential Health HazardOngoing
Refund