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. 1,747 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
1,747 in last 12 months

Showing 4474144760 of 49,677 recalls

DrugAugust 6, 2013· Novartis Consumer Health

Recalled Item: Maalox Regular Strength Antacid (calcium carbonate) chewable tablets...

The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or...

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2013· Novartis Consumer Health

Recalled Item: Maalox Nighttime Antacid with Acid Barrier (calcium carbonate and Recalled...

The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or...

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2013· Novartis Consumer Health

Recalled Item: Maalox Extra Strength Antacid (calcium carbonate) chewable tablets Recalled...

The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or...

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2013· Novartis Consumer Health

Recalled Item: Maalox Recalled by Novartis Consumer Health Due to Labeling: Incorrect Or...

The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or...

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2013· Novartis Consumer Health

Recalled Item: Maalox Nighttime Antacid with Acid Barrier (calcium carbonate and Recalled...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: The lot number and/or...

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2013· Novartis Consumer Health

Recalled Item: Maalox Advanced Maximum Strength Antacid & Antigas (calcium carbonate and...

The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or...

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2013· Showline Automotive Products, Inc. dba US Soaps Mfg. Company

Recalled Item: REEVA (triclosan) Antibacterial Hand Soap and Dishwashing Liquid Recalled by...

The Issue: Microbial Contamination of a Non-Sterile Products: Product was found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2013· Novartis Consumer Health

Recalled Item: Maalox Extra Strength Antacid with Anti-Gas (calcium carbonate and...

The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or...

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2013· Novartis Consumer Health

Recalled Item: Maalox Advanced Maximum Strength Antacid & Antigas (calcium carbonate and...

The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or...

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2013· Novartis Consumer Health

Recalled Item: Benefiber Recalled by Novartis Consumer Health Due to The lot number and/or...

The Issue: The lot number and/or expiration date may be illegible on the outer plastic...

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2013· Novartis Consumer Health

Recalled Item: Benefiber Recalled by Novartis Consumer Health Due to The lot number and/or...

The Issue: The lot number and/or expiration date may be illegible on the outer plastic...

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2013· Novartis Consumer Health

Recalled Item: Benefibre Recalled by Novartis Consumer Health Due to The lot number and/or...

The Issue: The lot number and/or expiration date may be illegible on the outer plastic...

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2013· Novartis Consumer Health

Recalled Item: Benefiber Recalled by Novartis Consumer Health Due to The lot number and/or...

The Issue: The lot number and/or expiration date may be illegible on the outer plastic...

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2013· Novartis Consumer Health

Recalled Item: Benefiber Recalled by Novartis Consumer Health Due to The lot number and/or...

The Issue: The lot number and/or expiration date may be illegible on the outer plastic...

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

Class III — Low RiskOngoing
Refund
DrugAugust 5, 2013· Bethel Nutritional Consulting, Inc

Recalled Item: Bethel Advance (bitter orange Recalled by Bethel Nutritional Consulting, Inc...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analyses detected the presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 5, 2013· Bethel Nutritional Consulting, Inc

Recalled Item: Quick Thin (citrus aurantium extract Recalled by Bethel Nutritional...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis detected the presence of...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 5, 2013· Toshiba American Medical Systems Inc

Recalled Item: Xario Diagnostic Ultrasound System SSA-660A Used for routine diagnostic...

The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· Medicel Ag

Recalled Item: Product Name: nanoPOINT Injector System Recalled by Medicel Ag Due to The...

The Issue: The firm initiated this recall of one lot (121402) of nanoPOINT Injectors...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· 3M Company/3m Espe Dental Products

Recalled Item: 3M ESPE Unitek Primary Stainless Steel Crowns (First Primary UL4) Recalled...

The Issue: 3M ESPE is recalling Unitek Primary Stainless Steel Crowns (First Primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· 3M Company - Health Care Business

Recalled Item: 3M Scotchcast Recalled by 3M Company - Health Care Business Due to 3M is...

The Issue: 3M is conducting a voluntary product recall of selected lots of 3M"...

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

Class II — Potential Health HazardOngoing