Recalls in Utah (page 32)
3917 recalls.
- GEM Premier 5000 PAK recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 PAK recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 PAK recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 PAK recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 PAK recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 PAK recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 PAK recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - Endo-Model Replacement Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model Replacement Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model Replacement Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model Replacement Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model Replacement Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model Replacement Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model Replacement Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model Replacement Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model Replacement Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model SL Connection Component incl. PE-Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model SL Connection Component incl. PE-Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model Replacement Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model SL Connection Component incl. PE-Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Raz-AT recall (Raz Design Inc)
Medical deviceClass IIReported March 18, 2026 · Due to a modification by a vendor and may be reinstalled without properly engaging the outside rear seat brackets that are used to keep the seat in place. - IBA Proton Therapy System - PROTEUS 235 recall (Ion Beam Applications S.A.)
Medical deviceClass IIReported March 18, 2026 · It was identified that eh Universal Beam Triggering Interface (UBTI) is disabled in the Therapy Safety System (TSS) configuration. In this condition, the TSS... - 10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk... recall (Becton Dickinson & Company)
Medical deviceClass IIReported March 18, 2026 · During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes. - LFTE USA Recalls Playground Swing Set Seats Due to Fall Hazard
Consumer productReported March 13, 2026 · The rivets used to support the swing seat can fail, posing a fall hazard to children. - 17 Stories Furniture 14-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units; Imported by Hong Kong Baojia International
Consumer productReported March 12, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - LIVEHOM 11-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units; Sold on Amazon by Simplehome
Consumer productReported March 12, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - ProRider Recalls Bicycle Helmets Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets
Consumer productReported March 12, 2026 · The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation, positional... - Stoney Games Recalls Kluster Magnet Chess Games Due to Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys
Consumer productReported March 12, 2026 · The recalled magnet games violate the mandatory standard for toys because they contain loose high-powered magnets that fit within CPSC's small parts cylinder... - Lobster & Crab Ravioli. Keep Frozen. Contains: Wheat recall (Perfect Pasta, Incorporated)
FoodClass IReported March 11, 2026 · Undeclared shrimp, crab, lobster, pollock (fish), whiting (fish), and soy. - Gelsoft Plus recall (Vascutek, Ltd.)
Medical deviceClass IIReported March 11, 2026 · Gelatin sealed woven polyester prostheses devices, designed for vascular repair, were incorrectly labeled with an additional month of shelf life. Device expiry... - Brand Name: STA Liatest Free Protein S Product Name: STA Liatest Free Protein S ... recall (Diagnostica Stago, Inc.)
Medical deviceClass IIReported March 11, 2026 · The potential of out-of-range results and an underestimation of the free protein S level in normal patient plasmas. The defect only affects normal-range values. - Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM ... recall (Aesculap Inc)
Medical deviceClass IIReported March 11, 2026 · There is the potential for the length of the trocar shaft to be too long. - Amnesteem recall (MYLAN PHARMACEUTICALS INC)
DrugClass IIReported March 11, 2026 · Failed Dissolution Specifications - Sodium Iodide recall (Radnostix)
DrugClass IIReported March 11, 2026 · Presence of Particulate Matter: Due to production issues - MAXIMUM recall (HTO Nevada Inc. dba Kirkman)
DrugClass IIReported March 11, 2026 · Stability Data Does Not Support Expiry Date. - MAXIMUM recall (HTO Nevada Inc. dba Kirkman)
DrugClass IIReported March 11, 2026 · Stability Data Does Not Support Expiry Date. - FIVE-STAR recall (HTO Nevada Inc. dba Kirkman)
DrugClass IIReported March 11, 2026 · Stability Data Does Not Support Expiry Date. - Product label: Temozolomide Capsules recall (Rising Pharma Holding, Inc.)
DrugClass IIReported March 11, 2026 · Failed Impurities/Degradation Specifications: An out-of-specification result observed during 9th-month long term stability testing - Midodrine Hydrochloride Tablets recall (The Harvard Drug Group LLC)
DrugClass IIReported March 11, 2026 · Defective container; inadequately sealed blister packaging. - Nilotinib Capsules recall (Cipla USA, Inc.)
DrugClass IIIReported March 11, 2026 · Failed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual Inspection... - Nilotinib Capsules recall (Cipla USA, Inc.)
DrugClass IIIReported March 11, 2026 · Failed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual Inspection... - Semaglutide recall (Harbin Jixianglong Biotech Co., Ltd.)
DrugClass IIReported March 11, 2026 · CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before distribution - Semaglutide recall (Harbin Jixianglong Biotech Co., Ltd.)
DrugClass IIReported March 11, 2026 · CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before distribution - Antimicrobial Alcohol Hand Wipe recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Children's Healthcare of Atlanta recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Dynarex recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Dynarex recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Green Guard Antiseptic Wipes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Hand Sanitizing Wipes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - WP WipesPlus Hand Sanitizing Wipes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Med-Nap Cleansing Towelettes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Cleansing Towelette recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Dynarex Obstetrical Towelettes Cleanser recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Wipes Plus recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - BZK Antiseptic Towelettes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Med Nap BZK Antiseptic Towelettes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Medi-First Antiseptic Wipes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Savannah Antibacterial Towelettes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Max Packaging Antibacterial Towelette recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - 1) BZK Antiseptic Towelettes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - First Aid Only BZK Antiseptic Towelette recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Dukal BZK Antiseptic Towelette recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - First Aid Only BZK Antiseptic Towelettes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - First Aid Only BZK Antiseptic Towelettes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Metoprolol Succinate Extended-Release Tablets recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported March 11, 2026 · Failed Dissolution Specifications - Metoprolol Succinate Extended-Release Tablets recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported March 11, 2026 · Failed Dissolution Specifications - Metoprolol Succinate Extended-Release Tablets recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported March 11, 2026 · Failed Dissolution Specifications - Metoprolol Succinate Extended-Release Tablets recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported March 11, 2026 · Failed Dissolution Specifications - Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units per box. ... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported March 11, 2026 · Potential for rubber fragment detachment during use. - Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units per box. ... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported March 11, 2026 · Potential for rubber fragment detachment during use. - CS300 IABP. Software Version CS300 IABP C.01. recall (Datascope Corp.)
Medical deviceClass IIReported March 11, 2026 · The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated. - CS100 IABP. Software Version CS100 IABP Q.01. recall (Datascope Corp.)
Medical deviceClass IIReported March 11, 2026 · The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated. - Atellica CH Urine Albumin recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported March 11, 2026 · Falsely depressed UAlb patient results may occur. Affected samples with any urine albumin concentration above the UAlb measuring interval >40.0 mg/dL may... - Brand Name: B. Braun Product Name: 21GA WINGED INF SET Model/Catalog Number: 7M2802 ... recall (B Braun Medical Inc)
Medical deviceClass IIReported March 11, 2026 · The potential for the needle tip to be dull/blunt, difficult to advance, and/or break. - Brand Name: B. Braun Product Name: 21GA WINGED INFUSION recall (B Braun Medical Inc)
Medical deviceClass IIReported March 11, 2026 · The potential for the needle tip to be dull/blunt, difficult to advance, and/or break. - Brand Name: B. Braun Product Name: BBraun Medical 21G X4.4CM Winged INF ... recall (B Braun Medical Inc)
Medical deviceClass IIReported March 11, 2026 · The potential for the needle tip to be dull/blunt, difficult to advance, and/or break. - Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE Lithotripsy... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported March 11, 2026 · Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer. Damage to the... - Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name: ShockPulse-SE... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported March 11, 2026 · Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer. Damage to the... - Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name: ShockPulse-SE... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported March 11, 2026 · Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer. Damage to the... - cobas pro integrated solutions with cobas c 503 analytical units: cobas pro sample... recall (Roche Diagnostics Operations, Inc.)
Medical deviceClass IIReported March 11, 2026 · Software defect, which allows the system to accept erroneous, non-monotonous calibrations for Spline-type assays. Cobas pro integrated solutions is an... - GE Healthcare Centricity Universal Viewer Zero Footprint Client recall (GE Healthcare)
Medical deviceClass IIReported March 11, 2026 · Under certain workflows, patient information shown in the viewer may not match the images displayed on Centricity Universal Viewer Zero Footprint Client (ZFP)... - Impella RP. Product Code: 0046-0011. recall (Abiomed, Inc.)
Medical deviceClass IReported March 11, 2026 · Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift. - Impella RP Flex with SmartAssist. Product Code: 1000323. recall (Abiomed, Inc.)
Medical deviceClass IReported March 11, 2026 · Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift. - Impella RP with SmartAssist. Product Code: 0046-0035. recall (Abiomed, Inc.)
Medical deviceClass IReported March 11, 2026 · Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift. - Cubimana Island Storm 3 In 1 Building Sets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by RBS Toys
Consumer productReported March 5, 2026 · The Island Storm Building Sets violate the mandatory safety standard for toys because the battery compartment within the LED light piece contains button cell... - HALO Dream Recalls Magic Sleepsuits Due to Choking Hazard
Consumer productReported March 5, 2026 · The zipper head can detach from certain sleepsuits, posing a choking hazard to infants. - Tomum Minoxidil Hair Serum Spray Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Distributed by Belleka
Consumer productReported March 5, 2026 · The hair serum contains minoxidil, which must be in child-resistant packaging as required by the Poison Prevention Packaging Act. The hair serum's bottles are... - Unique Brands Com Recalls Forever 21 Pajama Pants Due to Risk of Serious Injury or Death from Burn Hazard; Violates Mandatory Flammability Standards for Children's Sleepwear
Consumer productReported March 5, 2026 · The recalled children's pajama pants violate the mandatory standards for flammability of children's sleepwear, posing a burn hazard and risk of serious injury... - Gerber Arrowroot Biscuits recall (Gerber Products Company dba Nestle Infant Nutrition)
FoodClass IIReported March 4, 2026 · Downstream recall. Product contains arrowroot flour ingredient that was voluntarily recalled by the supplier due to potential contamination of soft kraft... - BioGlo Fluorescein Sodium Ophthalmic Strips USP recall (Wizcure Pharmaa Private Limited)
DrugClass IIReported March 4, 2026 · Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices. - Bio Glo Fluorescein Sodium Ophthalmic Strips USP recall (Wizcure Pharmaa Private Limited)
DrugClass IIReported March 4, 2026 · Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices. - CHNaO Fluorescein Sodium Ophthalmic Strips recall (Wizcure Pharmaa Private Limited)
DrugClass IIReported March 4, 2026 · Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices. - Vista Gonio Eye Lubricant recall (Wizcure Pharmaa Private Limited)
DrugClass IIReported March 4, 2026 · Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices. - Vista Meibo Tears Propylene Glycol 0.6% w/v Eye Drops Advanced Dry Eye Relief... recall (Wizcure Pharmaa Private Limited)
DrugClass IIReported March 4, 2026 · Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices. - Vista Gel Hypromellose USP 0.3% w/v recall (Wizcure Pharmaa Private Limited)
DrugClass IIReported March 4, 2026 · Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices. - Vista Tears Polyethylene Glycol 400 0.4% w/v recall (Wizcure Pharmaa Private Limited)
DrugClass IIReported March 4, 2026 · Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices. - Eptifibatide Injection recall (Slate Run Pharmaceuticals)
DrugClass IIIReported March 4, 2026 · Labeling: Not Elsewhere Classified. The carton for Eptifibatide Injection 75 mg/100 mL states 75 mg/100 mL vial for weight-adjusted bolus dosing. The approved... - Amantadine HCl recall (AvKARE)
DrugClass IIReported March 4, 2026 · Failed Dissolution Specifications: This recall has been initiated due to an Out of Specification finding in dissolution. - Adbry recall (LEO PHARMA INC)
DrugClass IIReported March 4, 2026 · Lack of Assurance of Sterility: due to the presence of particulate matter in one unit from the lot, which lab tests have identified as wool fiber. - Campy CVA Medium 100/PK recall (Remel, Inc)
Medical deviceClass IIReported March 4, 2026 · Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.