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. 2,563 recalls have been distributed to Utah in the last 12 months.
Showing 16281–16300 of 28,579 recalls
Recalled Item: SnapLock" Catheter/Syringe Adapter Recalled by Arrow International Inc Due...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 cc Luer-Slip Loss of Resistance Syringe Recalled by Arrow International...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Quad-Lumen Central Venous Catheterization Kit with Blue...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arterial Line Kit with Sharps Safety Features and Maximal Barrier...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Two-Lumen Central Venous Catheterization Kit with Blue...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximal Barrier Drape Recalled by Arrow International Inc Due to Product...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi-Lumen Central Venous Catheterization Kit Recalled...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spring-Wire Guide Introducer Catheter Assembly Recalled by Arrow...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit with Sharps Safety Features Recalled by...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R)...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 3.5MM...
The Issue: There is a potential for improper welding of the yellow staple guide to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 4.8MM...
The Issue: There is a potential for improper welding of the yellow staple guide to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HLD Systems 600 Series Washer/Pasteurizer Recalled by Cenorin, LLC Due to...
The Issue: There is a supplier quality issue with the terminal blocks which may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyTouch (ET) Insulin Syringe 29G 1ml ¿" (Item 829155) Product Recalled by...
The Issue: The retail shelf cartons may be labeled with an incorrect lot number.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyTouch (ET) Insulin Syringe 29G 0.5ml ¿" (Item 829555) Product Recalled...
The Issue: The retail shelf cartons may be labeled with an incorrect lot number.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoratec HeartMate 3 LVAS Implant Kit Recalled by Abbott Due to Reports of...
The Issue: Reports of outflow graft twist occlusions. Patients whose devices experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS IMRI 1.5T AND 3T S System Product Usage: The Recalled by Deerfield...
The Issue: The DC power to the IFOSS collision detector control panel at your facility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein CU 1000 Halogen Curing Light Recalled by Handpiece Headquarters...
The Issue: Tip of the curing light was too hot causing a heat sensation in the patients.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELLSEARCH¿ CIRCULATING Tumor Cell Kits (IVD) (Product Code 7900001)...
The Issue: Unusually high number of total images/unassigned events may require...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.