State

Utah product recalls

20,371 recalls have nationwide distribution and so reach Utah. 0 additional recalls listed Utah specifically in their distribution scope.

About recalls in Utah

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Utah consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

16026–16050 of 20371

ModerateFDA (Devices)·Z-1539-2022·2022-08-24
Poligrip Denture Adhesive Products Recalled for Improper Storage Conditions
Family Dollar Stores recalls multiple Poligrip denture adhesive products due to improper storage outside temperature-controlled areas. Affected products were sold between May 1 and June 10, 2022.
Product
POLIGRIP ADH CREAM FREE 2.4OZ, SKU 900334 POLIGRIP DENTURE ADHESIVE ORIGINAL 2.4OZ, SKU 900723 SUPER POLIGRIP ADH CREAM .75OZ, SKU 900085
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1540-2022·2022-08-24
Contact Lens Solution Recalled for Improper Temperature Storage
OPTI FREE REPLENISH contact lens solution sold at Family Dollar stores (May 1–June 10, 2022) was not stored in temperature-controlled areas and is being recalled.
Product
OPTI FREE REPLENISH MULTI PURPOSE 2 OZ
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1533-2022·2022-08-24
Clear Eyes Contact Lens Drops Recalled for Improper Storage
Family Dollar Stores is recalling Clear Eyes Contact Lens Drops Lubricating due to improper storage in non-temperature-controlled areas. The product was sold nationwide between May 1 and June 10, 2022.
Product
CLEAR EYES CONTCT LENS DRPS LBRCTNG .5FO, SKU 900531
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1547-2022·2022-08-24
KY Jelly Lubricant Recalled for Improper Storage Conditions
KY Jelly Lubricant 2 FL OZ (SKU 901443) distributed at Family Dollar stores was not stored in temperature-controlled areas. Consumers should discontinue use of product purchased between May–June 2022.
Product
KY JELLY LUBRICANT 2 FL OZ, SKU 901443
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1335-2022·2022-08-24
Drug Recall: Incorrect Syringe in ZYNRELEF Anesthetic Delivery Kits
Heron Therapeutics is recalling 1,790 kits of ZYNRELEF (bupivacaine and meloxicam) distributed nationwide because one lot contains an incorrect syringe in the delivery system. No illnesses or injuries have been reported.
Product
ZYNRELEF — ZYNRELEF (BUPIVACAINE AND MELOXICAM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1343-2022·2022-08-24
Rifampin Capsules Recalled Due to Manufacturing Control Deviation
Lupin Pharmaceuticals is recalling Rifampin 150 mg capsules (lot #A200170) nationwide due to a Current Good Manufacturing Practice deviation with an out-of-specification impurity detected during manufacturing.
Product
RIFAMPIN — RIFAMPIN (RIFAMPIN)
Category
Drug
Distribution
Distributed nationwide
HighCPSC·22202·2022-08-18
Hard Rock Cafe Children's Hooded Sweatshirts Recalled for Strangulation Hazard
Hard Rock Cafe is recalling about 1,550 children's hooded sweatshirts with drawstrings in the hood that can become entangled or caught on objects, posing a strangulation hazard to children. No injuries have been reported.
Product
Hard Rock Cafe Children's Hooded Sweatshirts
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·22201·2022-08-18
ASUS ROG Maximus Z690 Hero Motherboards Recalled for Fire and Burn Hazards
ASUS Computer International is recalling about 10,000 ASUS ROG Maximus Z690 Hero motherboards because a capacitor installed in reverse position can cause short circuits, overheating, or melting. ASUS has received 10 reports of overheating and melting, though no injuries have been reported.
Product
ASUS ROG Maximus Z690 Hero Motherboards
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1400-2022·2022-08-17
Viral Transport Container Distributed Without FDA Clearance or Guidance Compliance
Haimen Shengbang Laboratory Equipment recalled 100,000 viral transport containers distributed without FDA clearance and outside FDA guidance, affecting facilities in California, Florida, Illinois, New York, and China.
Product
HXBL/WETEX/Genesis Biomedical Viral Transport Container, Custom Made
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1398-2022·2022-08-17
FDA Recalls Viral Transport Containers Distributed Without Clearance
FDA recalls approximately 8.7 million viral transport containers that were distributed without regulatory clearance and without complying with FDA guidance for proper viral transport specifications.
Product
HXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59 Activated Type
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1399-2022·2022-08-17
FDA Recalls 3.95 Million Viral Transport Containers Distributed Without Clearance
The FDA recalled 3.95 million viral transport containers distributed without FDA clearance and in violation of established guidance. The containers were distributed worldwide, including to facilities in California, Florida, Illinois, and New York.
Product
HXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59-1
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1506-2022·2022-08-17
HAIOU Retractable Safety Syringes Recalled for Needle Detachment Risk
HAIOU retractable safety syringes are recalled due to reports of needle detachment from the syringe after injection and failure to retract, increasing needle stick injury risk. Approximately 4.05 million units are affected.
Product
HAIOU Needle retractable safety syringe with needle-(1ml syringe with 25G x 1-inch needle} 200 pieces/box. Intended Use: Disposable sterile needle retractable safety syringe. Catalog Number: NRSS1-25G25
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1331-2022·2022-08-17
FentaNYL Citrate IV solution recalled due to sterility assurance concerns
SterRx is recalling FentaNYL Citrate intravenous bags (10 mcg/mL) due to lack of assurance of sterility. The recalled lot (CHI, expiring December 2022) was distributed nationwide.
Product
FentaNYL Citrate in 0.9% Sodium Chloride 1 mg per 100 mL (10 mcg per mL) IV bags, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY, 12903, NDC 70324-327-01.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1511-2022·2022-08-17
GE Healthcare CT, PET, and NM Patient Tables May Drop During Service
GE Healthcare patient tables used in CT, PET, and NM systems can drop during service if technicians remove incorrect screws without appropriate supports, potentially injuring service personnel.
Product
Service manuals for the CT, PET, or NM table as follows: GT1700/GT1700V/VT1700, GT2000/VT2000, GT2000x/VT2000x, High Capacity Table, Lite Table, Kunlun Table, Global PET-CT Table, NP Table, P2005AA Table, LCT Table, CTE TWIN TABLE Assy. All devices are patient tables for PET/
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1330-2022·2022-08-17
Prednisone Tablets Recalled for Contamination With Wrong-Strength Tablets
Strides Pharma is recalling Prednisone 20 mg tablets due to contamination with 2.5 mg tablets. No illnesses have been reported, but patients may receive incorrect doses.
Product
PREDNISONE — PREDNISONE (PREDNISONE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1315-2022·2022-08-17
Eye-stream Eye Wash Solution Recalled for Improper Storage
Mckesson Medical-Surgical has recalled Eye-stream eye wash solution nationwide due to storage conditions outside drug label specifications.
Product
Eye-stream, eye wash solution, sterile, 4 FL OZ (118 mL) bottle per box, Alcon, NDC 0065-0530-04.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1515-2022·2022-08-17
Roche cobas e801 Analyzer Recall: Software Defect Affects Test Results
Roche is recalling approximately 965 cobas e801 Immunoassay Analyzers nationwide due to a software issue that impacts Pre-Wash test signals and results for six diagnostic assays. No injuries or illnesses have been reported.
Product
cobas e801 Immunoassay Analyzer
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1514-2022·2022-08-17
Lithotripsy Generator Recall Due to Mis-Wired Component Affecting System Reliability
Olympus Corporation recalls 2 units of the ShockPulse-SE Lithotripsy Generator due to a mis-wired component that causes improper power supply noise and EMC non-compliance, potentially affecting device reliability and treatment delivery.
Product
ShockPulse-SE Lithotripsy Generator Model/Serial: SPL-S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1507-2022·2022-08-17
Haiou Needle Retractable Safety Syringe recalls due to needle detachment risk
Approximately 7,218,000 Haiou Needle Retractable Safety Syringes are being recalled due to needle detachment and retracting mechanism failures that increase needlestick injury risk. The affected product was distributed in California.
Product
Haiou Needle Retractable Safety Syringe with Needle-1ML 23G x 1 (0.6x25mm). 200pcs/Box Intended Use: Disposable sterile needle retractable safety syringe. Catalog Number: NRSS1-23G25
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1513-2022·2022-08-17
Xhibit Telemetry Receiver Model 96280 alarm escalation software defect
Xhibit Telemetry Receiver Model 96280 units fail to escalate critical alarms after approximately 25 days of continuous use, including signal loss, low battery, and SpO2 sensor issues. Caregivers may not be aware of device failures.
Product
Xhibit Telemetry Receiver, Model: 96280
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1313-2022·2022-08-17
Eye Drops Recalled Due to Improper Storage Violating Manufacturing Standards
Naphcon A eye drops are being recalled nationwide because products were stored outside label specifications, violating Current Good Manufacturing Practice (CGMP) standards.
Product
NAPHCON A — NAPHCON A (NAPHAZOLINE HYDROCHLORIDE AND PHENIRAMINE MALEATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1539-2022·2022-08-17
Natierra Organic Freeze-Dried Blueberries Recalled for Lead Contamination
Natierra Nature & Earth Organic Blueberries are recalled due to elevated lead levels detected by Maryland Department of Health testing. The recall affects 22,014 units distributed nationwide.
Product
Natierra Nature & Earth Organic Blueberries Ingredients: Organic Freeze-Dried Blueberries NET WT 12 oz (34g) Distributed by Natierra Van Nuys, CA 91405-1545 Certified Organics by SCS Global Services Product of US, Canada, Poland, Estonia, Romania
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1326-2022·2022-08-17
FDA Recalls Sterile Alcohol Prep Pads Due to Improper Storage
Mckesson Medical-Surgical is recalling ALCOHOL PREP sterile alcohol prep pads nationwide because they were stored outside manufacturer specifications, potentially compromising sterility. FDA classified this as a Class II recall.
Product
ALCOHOL PREP — ALCOHOL PREP (ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1310-2022·2022-08-17
Lorazepam Injection Recalled for Out-of-Specification Impurities and Degradation
Hikma Pharmaceuticals is recalling 82,700 vials of Lorazepam Injection due to failed quality specifications for impurities and degradation. Lot #070096 (expired July 2023) was distributed nationwide.
Product
LORAZEPAM — LORAZEPAM (LORAZEPAM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1328-2022·2022-08-17
Difluprednate eye drops recalled for defective container closure affecting sterility
Cipla is recalling Difluprednate ophthalmic emulsion nationwide due to defective container closures that compromise sterility assurance. Patients using the affected lot should discontinue use and contact their healthcare provider.
Product
DIFLUPREDNATE — DIFLUPREDNATE (DIFLUPREDNATE)
Category
Drug
Distribution
Distributed nationwide