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 21061–21080 of 28,579 recalls
Recalled Item: Ottobock Modular Polycentric EBS Knee Joint 3R60 Recalled by Otto Bock...
The Issue: Otto Bock HealthCare GmbH is recalling Modular Polycentric EBS Knee Joint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toomey Syringe 70cc Syringe with Catheter Tip and Luer Tip Adapters Recalled...
The Issue: Report by a customer of an open package seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue Module Measurement X2 Model: M3002A Recalled by Philips...
The Issue: The ST elevation alarm on the Patient Monitor or standalone X2 Measurement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue Measurement Module X1 Model: M3001A Recalled by Philips...
The Issue: The ST elevation alarm on the Patient Monitor or standalone X2 Measurement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORDIS AVANTI + CATHETER SHEATH INTRODUCER SYSTEM The product includes...
The Issue: Incorrect cannula of the sheath introducer (smaller than intended).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This reagent is for in vitro diagnostic use. Pax-5 (1EW) Recalled by Leica...
The Issue: The Bond" Polymer Detection and Novolink" Polymer Detection System may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur PSA Assay Recalled by Siemens Healthcare Diagnostics, Inc Due...
The Issue: PSA assay is not meeting the High Dose Hook Effect expectation in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQURE System Recalled by Radiometer America Inc Due to The AQURE System has...
The Issue: The AQURE System has a design error regarding sample type in which sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PharmaCaribe PulmoSal 7% Sodium chloride Recalled by Pharmacaribe llc Due to...
The Issue: Vials were labeled as USP 7% Hypertonic saline instead of PulmoSal 7% (pH+)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EliA SmDP Well Recalled by Phadia Ab Due to All equivocal and positive...
The Issue: All equivocal and positive results (greater or equal 7 EliA U/ml) on EliA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548790 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548300 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549560 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Moog Curlin Infusion Recalled by MOOG Medical Devices Group Due to Moog is...
The Issue: Moog is recalling Curlin 4000, 6000, and PainSmart Infusion Pumps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548920 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548750 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548560 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549390 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548850 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549570 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.