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. 1,075 recalls have been distributed to Utah in the last 12 months.
Showing 14341–14360 of 49,677 recalls
Recalled Item: Artis Q ceiling with software VD12-angiography systems developed for single...
The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q.zen floor with software VD12-angiography systems developed for...
The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee multi-purpose with software VD12-angiography systems developed for...
The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gatifloxacin Ophthalmic Solution Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: Failed Stability Specifications: Out-of-specification results observed in a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diclofenac Sodium Topical Solution USP Recalled by Teligent Pharma, Inc. Due...
The Issue: Defective Container
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cubicin (daptomycin for injection) Recalled by MERCK SHARP & DOHME CORP Due...
The Issue: Presence of Particulate Matter: Identified as Glass Particles
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diclofenac Sodium Topical Solution USP Recalled by Teligent Pharma, Inc. Due...
The Issue: Defective Container
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nimbus PainPro Ambulatory Infusion Pumps with software version v4 Recalled...
The Issue: An unreleased Version 4 Protocol Library was installed on Nimbus PainPro (H)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model B35200 - Percept PC BrainSense Implantable Neurostimulator Recalled by...
The Issue: During cardioversion events, the Model B35200 Percept PC Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas u 601 urinalysis test system Recalled by Roche Diagnostics Operations,...
The Issue: A potential risk for false negative nitrite results exists when endogenous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rizatriptan Benzoate Orally Disintegrating Tablets 5mg Recalled by MACLEODS...
The Issue: Out-of-specification test results obtained in Organic Impurities test during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rizatriptan Benzoate Film Coated Tablets Recalled by MACLEODS PHARMA USA,...
The Issue: Out-of-specification test results obtained in Organic Impurities test during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rizatriptan Benzoate Orally Disintegrating Tablets 10mg Recalled by MACLEODS...
The Issue: Out-of-specification test results obtained in Organic Impurities test during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dimension Vista 1500 In-vitro diagnostic device intended to duplicate manual...
The Issue: Incorrect Default Hemolysis, Icterus or Lipemia (HIL) Index for Five...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500- In-vitro diagnostic device intended to duplicate manual...
The Issue: Incorrect Default Hemolysis, Icterus or Lipemia (HIL) Index for Five...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Anti-HBc IgM Controls Recalled by...
The Issue: Ortho Clinical Diagnostics confirmed a complaint that some VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endurant Stent Graft System REF/Description: ENTF2525C70EE STENT GRAFT...
The Issue: During stent graft deployment, the spindle may detach from the distal end of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endurant II Stent Graft System REF/Description: ETBF2513C145EE STENT GRAFT...
The Issue: Due to, during stent graft deployment, the spindle may detach from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Centricity Universal Viewer Zero Footprint Client Recalled by GE...
The Issue: There is a potential to display incomplete patient imaging study.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endurant IIs Stent Graft System REF/Description: ESBF2814C103EE STENT GRAFT...
The Issue: Due to, during stent graft deployment, the spindle may detach from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.