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. 2,495 recalls have been distributed to Utah in the last 12 months.
Showing 20821–20840 of 28,579 recalls
Recalled Item: iConnect Access used with Ortho PACS software provides medical specialists...
The Issue: Studies that are viewed in iConnect Access that originate on Merge PACS /...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADstream software. The firm name on the label is Merge Healthcare Recalled...
The Issue: The software was not presenting the PURE filter user interface message on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS software. The firm name on the label is Merge Healthcare Recalled...
The Issue: A migrated study that has annotations will display the annotations, but when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software. Product Usage: Merge Cardio is an integrated Recalled...
The Issue: Patient information in the header is only found on the first page of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge FlexConnect software Recalled by Merge Healthcare, Inc. Due to...
The Issue: Communication protocols interfacing with the affected software version with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge OfficePACS software. The firm name on the label is Merge Healthcare...
The Issue: Potential data loss occurs as a result of the software archiving not working...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iConnect Access used with Merge PACS software provides medical specialists...
The Issue: Studies that are viewed in iConnect Access that originate on Merge PACS /...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinity Acetabular System Product Usage - Total Hip Replacement. Recalled by...
The Issue: Potential for abrasion of the sterile barrier pouches of the new packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orapharma (Onpharma) Onset Mixing Pen Rx only Recalled by Valeant...
The Issue: It has been determined that the Onset Mixing Pen has an optimal use period...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinity Acetabular Shell Product Usage: Total Hip Replacement. Recalled by...
The Issue: Potential for abrasion of the sterile barrier pouches of the new packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinity Acetabular Shell Product Usage Total Hip Replacement. Recalled by...
The Issue: Potential for abrasion of the sterile barrier pouches of the new packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PINPOINT Endoscopic Fluorescence Imaging System Recalled by Novadaq...
The Issue: It has been determined that the PINPOINT Operator's Manual does not contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: software for Syngo Dynamics a Picture Archiving and Communication System...
The Issue: Siemens is releasing a software update that addresses an issue of mixing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GlideScope Titanium Single-Use Video Laryngoscope. It is a single-use video...
The Issue: The firm has become aware of the potential for disruption (flickering) in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crosslock DVR ePAK -Sterile Recalled by Biomet, Inc. Due to Foreign Object...
The Issue: Components of the DVR ePAKs can oxidize during shipment and storage prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK15 monitor/defibrillator with End-Tidal C02 (EtC02) feature...
The Issue: The firm became aware that when using EtC02 in the kPa or % setting and in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FMC7 FITC: Model 430918. FMC7 is intended for in Recalled by Becton,...
The Issue: Becton, Dickinson and Company (BD) has determined that the FMC7 FITC (ASR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Syngo Dynamics-a Picture Archiving and Communication System (PACS)...
The Issue: Siemens' conducting a recall due to a potential issue when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Dover PRECSION PRM 14FR SIL FLY Item Code: ¿ Recalled by Covidien...
The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Dover PREM U/M 14FR TMP SNS CSD Item Code: Recalled by Covidien LLC...
The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.