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. 2,361 recalls have been distributed to Utah in the last 12 months.
Showing 46981–47000 of 49,677 recalls
Recalled Item: KY SENSITIVE TM JELLY Personal Lubricant. The product is packaged Recalled...
The Issue: This product is not cleared for marketing in the US.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 700 Series Ventilators (PB740 and PB760) PB700 Series...
The Issue: Covidien is correcting labeling to clarify the operational life of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 840 Series Ventilator PB840 Operators Manual Addendum PN...
The Issue: Covidien is correcting labeling to clarify the operational life of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proplege Coronary Sinus Catheter model PR9 Recalled by Edwards Lifesciences,...
The Issue: Edwards Lifesciences is recalling certain Proplege Coronary Sinus Catheter,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KY SilkE Vaginal Moisturizer and Personal Lubricant. The product is Recalled...
The Issue: This product is not cleared for marketing in the US.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KY TINGLING JELLY Personal Lubricant. The product is packaged into Recalled...
The Issue: This product is not cleared for marketing in the US.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HLD System Recalled by Cenorin, LLC Due to The temperature sensor/control...
The Issue: The temperature sensor/control system in the HLD Systems Model 610 may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stelkast Cross-over Acetabular Shell and Liner Hip System Recalled by...
The Issue: Firm was made aware of incidents relating to the difficulty of properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D3000I Advantage Drive System Recalled by Linvatec Corp. dba ConMed Linvatec...
The Issue: The Membrane Switch Panel ( to as "front panel" of the component part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D3000 Advantage Drive System Recalled by Linvatec Corp. dba ConMed Linvatec...
The Issue: The Membrane Switch Panel ( to as "front panel" of the component part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sodium Sulfacetamide 10% and Sulfur 5% Lotion Recalled by Mission Pharmacal...
The Issue: Superpotent: Drug product active ingredients were formulated incorrectly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Terazosin Hydrochloride Capsules Recalled by Teva Pharmaceuticals USA, Inc....
The Issue: Presence of Foreign Tablets/Capsules: Recall is being conducted due to a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Crest PRO-HEALTH CPC Antigingivitis/Antiplaque Oral Rinse Recalled by...
The Issue: Cross Contamination with Other Products: Product was mixed with another type...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Plastic bottle containing 3.5 mL of IgG FITC Conjugate Product Recalled by...
The Issue: Affected products have a labeled expiration date of one year too long.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD Biopsy Systems (A Business Unit of Bard Peripheral Vascular Recalled by...
The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICROSHEATH¿ - 0.066 (1.7mm) proximal Recalled by Bard Peripheral Vascular...
The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: USHER¿ Support Catheter- Angled Tip WL130cm Recalled by Bard Peripheral...
The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD Biopsy Systems (A Business Unit of Bard Peripheral Vascular Recalled by...
The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plastic bottle containing 10.5 mL of IgG Conjugate Product Usage: Recalled...
The Issue: Affected products have a labeled expiration date of one year too long.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plastic bottle containing 10.5 mL of IgM Conjugate Product Usage: Recalled...
The Issue: Affected products have a labeled expiration date of one year too long.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.