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. 2,650 recalls have been distributed to Utah in the last 12 months.
Showing 3921–3940 of 28,579 recalls
Recalled Item: First Source Vision M. Portable cart and platform that supports Recalled by...
The Issue: Potential for the bolt that secures the positioning arm to the gas spring to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Source iQ Flex M. Portable cart and platform that Recalled by First...
The Issue: Potential for the bolt that secures the positioning arm to the gas spring to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Hoffman LRF Wire Tensioner Recalled by Stryker GmbH Due to The...
The Issue: The adjustment ring on the device may become loose resulting in the wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Medical SureStep Foley Tray System Recalled by C.R. Bard Inc Due to...
The Issue: Some of the devices may function incorrectly resulting in no temperature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Tempus LS-Manual Defibrillator Recalled by Remote Diagnostic...
The Issue: Simultaneous ECG measurements with multiple devices, including a manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Multitest 6-Color TBNK CE-IVD Recalled by Becton, Dickinson and Company,...
The Issue: Multitest with compromised raw material used to assess immune system status...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centrella Max - The Centrella Smart+ Bed is intended for Recalled by Baxter...
The Issue: There is a potential for the top cover of the hospital bed mattress to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoratec HeartMate System Monitor Recalled by Thoratec Corp. Due to System...
The Issue: System monitor screen may display atypical behavior: Overlapping...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. Reusable Patient...
The Issue: Reports of patient burns.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Vitamin B12 Range Verifier - In vitro...
The Issue: The results generated by the VITROS Immunodiagnostic Products Vitamin B12...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline ReNewal Reprocessed Covidien LigaSure Maryland Jaw Sealer/Divider...
The Issue: Potential for an incomplete seal on the packaging tray.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline ReNewal Reprocessed Covidien LigaSure Blunt Tip Recalled by MEDLINE...
The Issue: Potential for an incomplete seal on the packaging tray.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline ReNewal Reprocessed Covidien LigaSure Impact Recalled by MEDLINE...
The Issue: Potential for an incomplete seal on the packaging tray.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline ReNewal Reprocessed Ethicon Harmonic ACE+7 Shears w/ Adv. Hemostasis...
The Issue: Potential for an incomplete seal on the packaging tray.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replacement Battery List Number SUB0000594 and SUB0000864 found in Plum...
The Issue: Due to a manufacturing defect from the battery supplier, affected batteries...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum 360/A+ spare batteries. Item Number: SUB0000864. Recalled by ICU...
The Issue: Due to a manufacturing defect from the battery supplier, affected batteries...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replacement Battery List Number SUB0000864 Recalled by ICU Medical Inc Due...
The Issue: Due to a manufacturing defect from the battery supplier, affected batteries...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORI Starter Kit Recalled by Blue Belt Technologies, Inc Due to CORI...
The Issue: CORI Surgical System with Real Intelligence Software exhibits an increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN BACTISEAL EVD Catheter Set - Indicated for gaining access Recalled by...
The Issue: Defect in the external sterile packaging (pouch) leading to a gap or/and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN BACTISEAL Clear EVD Catheter 1.9mm I.D. Catheter Set- indicated...
The Issue: Defect in the external sterile packaging (pouch) leading to a gap or/and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.