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. 1,139 recalls have been distributed to Utah in the last 12 months.
Showing 2181–2200 of 49,677 recalls
Recalled Item: HME TwinStar HEPA Plus Filter. Bidirectionally breathing system filter....
The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: An out of specification results observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone 200 mg Pellet packaged in 1mL amber vials Recalled by Qualgen,...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date: A printing issue...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SafeStar 55 Plus Filter. Bidirectionally breathing system filter. Recalled...
The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SwabFlush Prefilled Syringe with ICU Medical SwabCaps Recalled by MEDLINE...
The Issue: SwabFlush syringes are affected by the ICU Medical recall of their SwabCap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano Visions Digital IVUS Catheter: PV.014P (Platinum) Recalled by...
The Issue: Reports of IVUS catheter and guide wire entanglement during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estrone RIA Catalog Number DSL8700 UDI Code: 15099590211615 Estrone RIA...
The Issue: Estrone RIA kit lots may rarely give falsely high patient results which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular Recalled...
The Issue: Due to packaging discrepancy with the incorrect tibial inserts/implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products OP Reagent Gen 15. Model Number: 680 Recalled by...
The Issue: Lots from Generation (GEN) 15 of VITROS Chemistry Products OP Reagent may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular Recalled...
The Issue: Due to packaging discrepancy with the incorrect tibial inserts/implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL Recalled by Johnson & Johnson Vision...
The Issue: Due to defects (bubbles/voids) identified during standard finished goods testing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endosee System Convenience Kit with IV Tube. Model Number: ES-TRAY-IV....
The Issue: The HSG Procedure Trays and Endosee System Convenience Kits contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASPRIRE Cristalle Mammography System (cleared under K212873) installed with...
The Issue: Devices had an unapproved slabbing software function enabled for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endosee System Convenience Kit. Model Number: ES-TRAY. Endosee System...
The Issue: The HSG Procedure Trays and Endosee System Convenience Kits contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Famciclovir Tablets Recalled by Macleods Pharmaceuticals Ltd Due to Presence...
The Issue: Presence of Foreign Substance- Black hair strand found attached to a tablet...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HSG Procedure Tray. Model Number: 6050T. The HSG Procedure Tray Recalled by...
The Issue: The HSG Procedure Trays and Endosee System Convenience Kits contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. Welby Vitamin B12 Adult Gummies 140 Count 2. Berkely Recalled by Vita...
The Issue: Contains undeclared peanut
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Caphosol Artificial Saliva (32 doses sachet box). 64 x 15 Recalled by...
The Issue: Out of specification stability test result for the Caphosol B solution from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BostonSight SCLERAL Lens Recalled by Boston Foundation For Sight Due to...
The Issue: Select orders of lenses were manufactured with errors impacting sagittal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BostonSight PROSE Lens. Recalled by Boston Foundation For Sight Due to...
The Issue: Select orders of lenses were manufactured with errors impacting sagittal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.