State

Utah product recalls

20,364 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.

14101–14125 of 20364

HighFDA (Devices)·Z-1168-2023·2023-03-01
Diagnostic imaging system recalled due to ceiling and wall collision risk
Siemens Uroskop Omnia Max imaging systems are recalled due to collision risk with ceilings, walls, or objects caused by default configuration settings. The systems may move dangerously, potentially injuring staff or patients.
Product
Uroskop Omnia Max with software VE10 & VF11- A diagnostic imaging system for radiographic and fluoroscopic studie Model Number:10762473
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1160-2023·2023-03-01
Respiratory care breathing circuits recalled for incorrect expiration date labeling
S & MOHR AMERICA recalled approximately 1,320 abm Respiratory Care Standard Breathing Circuits due to incorrect expiration dates printed on product labels. The manufacturing date was printed where the expiration date should appear.
Product
abm Respiratory Care Standart Breating Circuit with Face Mask - Toddler REF BC21087 abm Respiratory Care Standart Breathing Circuit with Face Mask - Child/Adult Small REF BC21088 abm Respiratory Care Standart Breathing Circuit with Face Mask - Adult Large REF BC21273 abm
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0329-2023·2023-03-01
OTC First Aid Spray Recalled for Subpotent Active Ingredient
Dermoplast FIRST AID spray is being recalled because testing found low levels of one of its two active ingredients. The product was distributed nationwide through internet, distributors, and retailers.
Product
DERMOPLAST FIRST AID — DERMOPLAST FIRST AID (BENZETHONIUM CHLORIDE AND BENZOCAINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0333-2023·2023-03-01
TIROSINT Levothyroxine Oral Solution Recalled for Subpotent Drug Content
IBSA PHARMA INC is recalling TIROSINT oral solution (Lot #220855) nationwide due to insufficient potency of levothyroxine sodium. The defective lot was voluntarily recalled after manufacturer discovery.
Product
TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0344-2023·2023-03-01
TIROSINT Levothyroxine Oral Solution Recalled for Subpotency
IBSA Pharma has recalled one lot of TIROSINT (levothyroxine sodium) oral solution nationwide due to subpotency. The product contained less active ingredient than labeled.
Product
TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0343-2023·2023-03-01
TIROSINT levothyroxine sodium oral solution recalled for subpotency nationwide
IBSA Pharma Inc. is recalling TIROSINT (levothyroxine sodium) oral solution due to subpotency—some doses contain insufficient active ingredient. Patients should contact their pharmacist or doctor to verify their medication.
Product
TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
CriticalCPSC·23136·2023-02-23
LumaRail Bed Assist Rails recalled for entrapment and asphyxia hazard
Platinum Health is recalling about 53,000 LumaRail bed assist rails because users can become entrapped between the rail and mattress, risking death by asphyxiation. One death has been reported.
Product
LumaRail Bed Assist Rails
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23132·2023-02-23
Zinus SmartBase Euro Slats Metal Platform Bed Frames Recalled for Collapse Hazard
Zinus is recalling about 30,400 SmartBase Euro Slats metal platform bed frames because missing reinforcing brackets can cause the frame to collapse, creating an injury hazard. Consumers should stop using the bed frames and request a free repair kit.
Product
SmartBase® Euro Slats Metal Platform Bed Frames
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23133·2023-02-23
1st Stage Scuba Regulators Recalled for Drowning and Injury Risk
XDEEP 1st stage scuba regulators (model NX700) are recalled because a defective screw on the turret connection can break, creating a risk of severe injury and drowning for divers.
Product
1st stage scuba regulators
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23130·2023-02-23
Two Million Cosori Air Fryers Recalled for Fire and Burn Hazards
Atekcity Corporation is recalling about 2 million Cosori air fryers because a wire connection can overheat, posing fire and burn hazards. The firm has received 205 reports of fires, with 10 minor burn injuries and 23 reports of minor property damage.
Product
Cosori Air Fryers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23134·2023-02-23
Lancaster Table & Seating High Chairs Recalled for Fall Hazard
Clark Associates is recalling Lancaster Table & Seating brand high chairs that can break during use, posing a fall hazard to children. Three reports of high chairs breaking have been received, though no injuries have been reported.
Product
Lancaster Table & Seating brand High Chairs
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23135·2023-02-23
Aderes Bookcases Recalled Due to Tip-Over and Entrapment Hazards
TJX is recalling about 73 Aderes bookcases that can tip over if not anchored to the wall, posing tip-over and entrapment hazards that can result in death or injuries to children. Two reports of unstable bookcases have been received with no injuries reported.
Product
Aderes bookcases
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23129·2023-02-23
Mainstays Three-Wick Candles Recalled for Fire and Laceration Hazards
Star Soap Star Candle Prayer Candle recalled about 1.2 million Mainstays Three-Wick Candles because the wicks can burn too close to the glass container, causing it to break and posing fire and laceration hazards. Consumers should stop using the candles immediately and request a refund.
Product
Mainstays Three-Wick Candles
Category
Consumer Product
Distribution
Distributed nationwide
ModerateCPSC·23131·2023-02-23
SCARPA F1 Ski Boots Recalled for Fall Hazard
SCARPA North America is recalling about 770 F1 LT and F1 GT ski boots manufactured in 2022. Screws attaching the ski/walk mechanism can loosen or fall out, causing the mechanism to malfunction and posing a fall hazard.
Product
F1 LT and F1 GT Ski Boots
Category
Consumer Product
Distribution
Distributed nationwide
ModerateCPSC·23728·2023-02-23
Polaris Timbersled Snow Bike Conversion Kits Recalled for Crash Hazard
Polaris is recalling about 780 Timbersled snow bike conversion kits because a QuickDrive fastener can loosen during operation, causing brake failure and crash risk. No crashes or injuries have been reported.
Product
Polaris Timbersled Snow Bike Conversion Kits
Category
Consumer Product
Distribution
Distributed nationwide
ModerateCPSC·23729·2023-02-23
Harbor Freight Replacement Lower Blade Guards for 12-Inch Miter Saws
Harbor Freight Tools is recalling replacement lower blade guards for 12-inch Chicago Electric Miter Saws because they do not sufficiently cover the saw blade and can break during use, posing an injury hazard.
Product
Replacement lower blade guards for 12-inch Chicago Electric Miter Saws
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1128-2023·2023-02-22
Surgical Convenience Kits Recalled Due to Non-Sterile Outer Packaging
Medline and Centurion Medical Products are recalling surgical convenience kits because the outer packaging has perforations that prevent sterility, leaving only the contents inside the kit wrapping sterile.
Product
Surgical convenience kits labeled as: a) MEDLINE HAND PACK, Reorder Number DYNJ67850; b) MEDLINE SHOULDER SUSPENSION II-LF, Reorder Number DYNJSHOULDER2; c) MEDLINE TRAY BONE MARRO ASC LTX SAFE, Reorder Number P429589A; d) MEDLINE LUMBAR TRAY, Reorder Number SPEC0177;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1114-2023·2023-02-22
Surgical Breast Biopsy Kits Recalled Due to Non-Sterile Outer Wrapping
Medline Industries is recalling 60 units of its Breast Biopsy Kit nationwide because the outer wrapping is not sterile. Only the kit's contents maintain sterility.
Product
Surgical convenience kits labeled as: MEDLINE BREAST BIOPSY KIT, Reorder Number DYNDA1224B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0293-2023·2023-02-22
Fluconazole 200mg injection recalled due to sterility concerns
Sentara Infusion Services is recalling Fluconazole 200mg injectable solution due to lack of sterility assurance. The recall affects 13 bags distributed nationwide to patients.
Product
FLUCONAZOLE 200MG NS 100ML, antifungal, Rx only, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1130-2023·2023-02-22
HydroPICC Catheter Recall Due to Incorrect Expiration Dates on Select Lots
Select lots of HydroPICC 4Fr catheters are mislabeled with expiration dates that exceed their actual expiration. Affected units should not be used.
Product
HydroPICC 4Fr Single Lumen, 80cm Guidewire - Basic Kit, Model Number 80001002
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1123-2023·2023-02-22
Surgical Convenience Kits Recalled for Outer Wrapping Sterility Defect
Medline is recalling 1376 surgical convenience kits nationwide due to a packaging defect that compromises the sterility of the outer wrapping. Only the kit contents remain sterile.
Product
Surgical convenience kits labeled as: MEDLINE PREP TRAY, Reorder Number DYNDL1643A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0269-2023·2023-02-22
Metoprolol Succinate ER Tablets Recalled for Failed Dissolution Specifications
Amerisource Health Services is recalling Metoprolol Succinate Extended-Release Tablets due to failed dissolution specifications that may prevent proper drug release.
Product
METOPROLOL SUCCINATE — METOPROLOL SUCCINATE (METOPROLOL SUCCINATE ER TABLETS)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0318-2023·2023-02-22
Sentara TPN Products Recalled Due to Lack of Sterility Assurance
Sentara Infusion Services is recalling 26 bags of Total Parenteral Nutrition (TPN) solutions distributed nationwide because the manufacturer cannot assure the products maintain sterility. Patients receiving these products should contact their healthcare provider.
Product
TPN (a) 100GM/AA, 285GM/DEX, (b)55GM/LIP 2300ML, (c)55GM/AA 285GM/DEX 50GM/LIP1800ML, (d)TPN AA:100GM DEX:250GM LIP:50GM 2400ML, (e) 55GM DEX:285GM 1800ML, Rx Only, use with Curlin pump or no pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeak
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0327-2023·2023-02-22
Abelcet Injectable Drug Recalled Due to Bacterial Contamination
A sterile injectable drug, Abelcet, is being recalled due to bacterial contamination detected in a nationwide shipment. The recall affects 31,879 vials with lot number 1203A.
Product
Abelcet (Amphotericin B Lipid Complex) Injection, 5 mg/mL, 100 mg vial, Rx only, Manufactured by Exelead, Inc., Indianapolis, IN 46268; Distributed by Leadiant Biosciences, Inc., Gaithersburg, MD 20878, NDC 57665-101-41
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0266-2023·2023-02-22
Injectable drug vials recalled for particulate matter contamination
McGuff Compounding Pharmacy Services is recalling Thiamine Hydrochloride and Riboflavin injection vials due to presence of foreign substances in some units.
Product
Thiamine Hydrochloride 200 mg/2mL (100mg/mL), Riboflavin 2 mg/2mL (1mg/mL) Injection, FOR INTRAMUSCULAR OR SLOW INTRAVENOUS USE, 2 mL Sterile Single Use Vial, Preservative-Free, Rx Only, Compounded for a licensed professional or patient use by: McGuff Compounding Pharmacy Service
Category
Drug
Distribution
Distributed nationwide