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. 2,397 recalls have been distributed to Utah in the last 12 months.
Showing 41681–41700 of 49,677 recalls
Recalled Item: Clonidine HCL Recalled by Gyma Laboratories Of Amer,Inc Due to cGMP...
The Issue: cGMP Deviations: GYMA laboratories Inc. has recalled multiple Active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Hulka Clip is a sterile packaged medical device that Recalled by Richard...
The Issue: Richard Wolf Medical Instrument Corporation is recalling Hulka Clip Tubal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene BC-GN Test Kit (Catalog number 20-005-021) includes: 1) 20 Recalled...
The Issue: Nanosphere Inc. has recently determined through four customer complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kodak DirectView DR 7500 Diagnostic X-Ray System Product Usage: The Recalled...
The Issue: An on-site evaluation of the equipment parts that attach the Beta Assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QLAB 10.1 Core Module PN 453561728001. QLAB Quantification Software is...
The Issue: The QLAB a2DQ and aCMQ features have a defect that may use incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QLAB 10 Core Module PN 453561704771. QLAB Quantification Software is...
The Issue: The QLAB a2DQ and aCMQ features have a defect that may use incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIRACEPT (R) (nelfinavir mesylate) Tablets Recalled by Pfizer Inc. Due to...
The Issue: Labeling: Incorrect or missing lot and or Exp Date: The bottles were labeled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shell Eggs packaged under the following labels: (1) Abbotsford Farms...
The Issue: Shell eggs contaminated with Pseudomonas fluorescens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Choripdong Chocolate Almond Richmond Ice Bar 4 bars/432 mL Seoul Recalled by...
The Issue: Seoul Trading USA Inc. is recalling Choripdong Chocolate Almond Richmond Ice...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gyrus ACMI Falope-Ring Dilator Recalled by Gyrus Medical, Inc Due to...
The Issue: Falope-Ring Dilator for Reusable Falope-Ring Band Applicators have been sold...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Specialty Aria Inserter Recalled by Stryker Spine Due to Stryker has...
The Issue: Stryker has initiated the recall of its Aria Standard and Specialty Implant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Luminos dRF Recalled by Siemens Medical Solutions USA, Inc Due to It...
The Issue: It was discovered that during a RAD examination using Siemens Luminos dRF,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Aria Implant Inserter Recalled by Stryker Spine Due to Stryker has...
The Issue: Stryker has initiated the recall of its Aria Standard and Specialty Implant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Possible sound loss...
The Issue: Possible sound loss associated with the CARESCAPE Monitor B650. When an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4051 Endo Tube Holder Recalled by Smiths Medical ASD, Inc. Due to The tube...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4002S Neonatal/Paed.Intubation Kit 3.0mm Murphy Recalled by Smiths Medical...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4052 Endo Tube Holder Recalled by Smiths Medical ASD, Inc. Due to The tube...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4002PS Neonatal/Paed.Intubation Kit 3.0mm Murphy Recalled by Smiths Medical...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4001PS Neonatal/Paed.Intubation Kit 2.5mm Murphy Recalled by Smiths Medical...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4001S Neonatal/Paed.Intubation Kit 2.5mm Murphy Recalled by Smiths Medical...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.