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 26861–26880 of 28,579 recalls
Recalled Item: Test Strips packaged in the OC-Light Manual iFOBT Kit Recalled by Polymedco,...
The Issue: The test strips in the affected product lots of the OC Light immunological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System. Radiation treatment planning. Recalled by Elekta, Inc....
The Issue: The beam is displayed at the "gantry" angle, but the dose is calculated at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANTI-BORRELIA (LYME) MICROPLATE EIA Kit Recalled by Innominata Dba Genbio...
The Issue: Multiple incidents of low-reacting assay plates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer NexPosure Recalled by Zimmer, Inc. Due to Possibility that the inner...
The Issue: Possibility that the inner pouch may be compromised. The product is packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic DBS Lead Kit for Deep Brain Stimulation Recalled by Medtronic...
The Issue: There is a potential for lead damage due to the use of the lead cap provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avex CX Suite Recalled by Ultradent Products, Inc. Due to Orthodontic...
The Issue: Orthodontic brackets distributed was incorrectly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic DBS Therapy for Dystonia Kit Recalled by Medtronic Neuromodulation...
The Issue: There is a potential for lead damage due to the use of the lead cap provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Ortho-Clinical Diagnostics, Inc. (OCD) determined that extension springs on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Spine Polaris 5.5 Button Lock Screw Inserter. Catalog Number Recalled...
The Issue: Increased risk of failure at the driver tip during screw insertion or removal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Ortho-Clinical...
The Issue: Ortho-Clinical Diagnostics, Inc. (OCD) determined that extension springs on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...
The Issue: Ortho-Clinical Diagnostics, Inc. (OCD) determined that extension springs on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CR MD1.0 General Set Recalled by AGFA Corp. Due to The cassettes were...
The Issue: The cassettes were shipped with the wrong IP (image plate) size bar code.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heritage Labs Path Study Extra Supplies Kit Recalled by Heritage Labs...
The Issue: The product has a Lithium Heparin contaminant which could adversely affect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smiths Medical Recalled by Smiths Medical ASD, Inc. Due to In rare...
The Issue: In rare instances, the BCI¿ Remote Alarm Cables (BCI¿ Cable) are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+3 Infusion Pump. List Number 12618. The Plum A+ Recalled by Hospira...
The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Hyperbaric Infusion Pump. List Number 11005. The Plum Recalled by...
The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Infusion Pump with Hospira MedNet Software. List Number Recalled by...
The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+3 Infusion Pump System. List Number 12348. The Plum Recalled by...
The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Infusion Pump. List Number 11973. The Plum A+ Recalled by Hospira...
The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Infusion Pump with Hospira MedNet Software. List Number Recalled by...
The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.