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. 2,453 recalls have been distributed to Utah in the last 12 months.
Showing 26801–26820 of 28,579 recalls
Recalled Item: Nova StatStrip Xpress Glu-Test Strips (Glucose test strips) Catalog # 42214...
The Issue: Glucose test strips reports no result message when tested
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeScan brand OneTouch¿ Ultra Control Solution Recalled by Lifescan Inc Due...
The Issue: When OneTouch¿ Ultra and OneTouch¿ Select test strips are tested with Ultra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GOPump Elastometric infusion PumpKit with/ and without accesssories all...
The Issue: Received 2 complaints out of 458 distributed pumps in this lot, where flow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeScan brand OneTouch¿ Select Control Solution Recalled by Lifescan Inc...
The Issue: When OneTouch¿ Ultra and OneTouch¿ Select test strips are tested with Ultra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duane Reade TRUEtrack monitor kit Recalled by Nipro Diagnostics, Inc. Due to...
The Issue: Meter kit outer boxes containing 10 ct. test strips state incorrect storage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boule Con-Diff Tri-Level Multi-Parameter Assayed Hematology Control Recalled...
The Issue: Elevated MCV results on the 1311-682, 1311-683, and 1311-684 lots.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Baseplate Impactor Extractor TRIATHLON Instruments....
The Issue: Stryker received reports from the field indicating that the handle detached...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 11-Hole Recalled by Synthes USA HQ, Inc. Due to The Synthes...
The Issue: The Synthes One-Third Tubular DCL Plate (11-Hole, 1/3 Tubular Plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aperio ScanScope System. Aperio ScanScope Models Recalled by Aperio...
The Issue: Aperio initiated this recall because the User Guides incorrectly state the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension(R) Phosphorus (PHOS) Flex(R) reagent cartridge (DF61) The...
The Issue: Siemens Healthcare Diagnostics has initiated a voluntary field action for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Radial Head Prosthesis: Trial Radial Head Elbow joint prosthesis:...
The Issue: The Trial Head may come loose from the implant stem during manipulation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerr Maxcem Elite Recalled by Kerr/Pentron, DBA Kerr Corporation and Pentron...
The Issue: Kerr Corporation is initiating this recall because raw material used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hickman 9.0 French Dual Lumen Catheter with SureCuff Tissue Ingrowth...
The Issue: Bard Access Systems is recalling two lots of Hickman 9.0 French and one lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension Vista(R) System Vista Drug 4 Calibrator. The device...
The Issue: Siemens has confirmed complaints of low QC and patient recovery with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leonard 10.0 French Dual Lumen Catheter with SureCuff Tissue Ingrowth...
The Issue: Bard Access Systems is recalling two lots of Hickman 9.0 French and one lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OsteoSelect DBM Putty Product Usage: Orthopedic bone filler Recalled by...
The Issue: The firm's retesting procedure was not validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.75mm x 12mm Fixed Cervical Screws. Components of the Genesys Recalled by...
The Issue: Manufacturing residue may be present on the cervical screws. Use of this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial baseplate Recalled by Orthopedic Alliance LLC Due to The recall of...
The Issue: The recall of the Loaner Bin and Sterilization Trays for implants and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12mm x 27mm x 8mm 12mm x 27mm x 9mm Recalled by Spinal Solutions, LLC Due to...
The Issue: The recall of the Loaner Bin and Sterilization Trays for implants and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 60 mm Rod Recalled by Spinal Solutions, LLC Due to The recall of the Loaner...
The Issue: The recall of the Loaner Bin and Sterilization Trays for implants and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.