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 4061–4080 of 28,579 recalls
Recalled Item: BSM-3000 Series Bedside Monitor The Life Scope BSM-3000 Recalled by Nihon...
The Issue: Due to software issue the device may give false "SpO2 Probe Failure" alarm
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow FiberOptix Intra-Aortic Balloon Catheter Kit: a) Recalled by ARROW...
The Issue: Teleflex received reports indicating an infrequent condition that, when not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow UltraFlex Intra-Aortic Balloon Catheter Kit Recalled by ARROW...
The Issue: Teleflex received reports indicating an infrequent condition that, when not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: GlideScope Core 15-inch FHD Model/Catalog Number: 0570-0437...
The Issue: Due to software issues, their is the potential for loss of image or a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Ultra 8 IAB Intra-Aortic Balloon Catheter Kit Recalled by ARROW...
The Issue: Teleflex received reports indicating an infrequent condition that, when not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: GlideScope Core 15-inch Monitor Model/Catalog Number: 0570-0404...
The Issue: Due to software issues, their is the potential for loss of image or a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDC Recalled by Centers For Disease Control and Prevention Due to The H5b...
The Issue: The H5b component may fail to amplify, resulting in an inconclusive result.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm O2 Imaging System-Mobile x-ray system designed for 2D fluoroscopic...
The Issue: Potential for an electrical component of the O-arm" O2 Imaging System to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EsoFLIP Recalled by Covidien, LLC Due to Due to saline conductivity issues,...
The Issue: Due to saline conductivity issues, their is a potential that dilation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STARDRIVE SCRWDRVR SHFT/T4 50MM/SELF-RETAINING/HXC-Intended for tightening...
The Issue: Stardrive Screwdrivers manufactured without a 5-degree relief cut around the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasySuite 4K Integrated Operating Room System Model/Catalog Number:...
The Issue: A subset of the ES4K systems do not have complete records for earth leakage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EsophaCap Product Name: EsophaCap (25mm diameter Recalled by...
The Issue: The EsophaCap sponge may be at increased risk of detaching from the string...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EsophaCap Product Name: EsophaCap (20mm diameter Recalled by...
The Issue: The EsophaCap sponge may be at increased risk of detaching from the string...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coviden Monoject 60ml Syringe Luer-Lock Tip-used to inject fluid into...
The Issue: Quarantined product was inadvertently distributed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo ProVue Recalled by Stryker Neurovascular Due to Neurovascular devices...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo Trak 21 Microcatheter Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro .014"guide wire Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DAC 044 115cm Recalled by Stryker Neurovascular Due to Neurovascular devices...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo NXT ProVue 3 x 32 Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo XP ProVue Retriever 4 x 20 Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.