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. 2,623 recalls have been distributed to Utah in the last 12 months.
Showing 10281–10300 of 28,579 recalls
Recalled Item: Steris CO2MPACT Endoscopic Insufflator system Recalled by Northgate...
The Issue: An internal tubing component in the flow path was made with incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed 50L abdominal insufflator Recalled by Northgate Technologies, Inc....
The Issue: An internal tubing component in the flow path was made with incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Screw 6.5x25mm - Product Usage: used as a sterile Recalled by...
The Issue: Zimmer Biomet is conducting a lot specific medical device recall for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MARQUEE Disposable Core Biopsy Instruments XX.Xcm Recalled by Bard...
The Issue: Due to the Penetration Depth Switch used to select the desired penetration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHYSIO CONTROL LIFEPAK CR2 Defibrillator 3321605-xxx The LIFEPAK CR2...
The Issue: Due to complaints received regarding missing lid magnets which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products VersaTips - Product Usage: used to dispense...
The Issue: A deformity affecting a specific lot of VITROS¿ Chemistry Products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power Injectable CT Port insertion kits - Product Usage: is Recalled by...
The Issue: The 5F Dignity CT Port kits were packaged with the incorrect size port. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Parietex hydrophilic anatomical mesh 15 cm x 10 cm Recalled by...
The Issue: incorrect device is contained in the package. The packaging label indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENROUTE Transcarotid Stent System Recalled by Silk Road Medical Inc Due to...
The Issue: Due to complaints received that the tip/nose cone may detach from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grasper/Retriever Recalled by Shent USA, Inc. Due to Mislabeling
The Issue: Mislabeled: Devices labeled as catalog #7208 (Grasper/Retriever, Alligator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grasper/Retriever Recalled by Shent USA, Inc. Due to Mislabeling
The Issue: Mislabeled: Devices labeled as catalog #7208 (Grasper/Retriever, Alligator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Natus Manufacturing Limited Due to The external drainage system...
The Issue: The external drainage system failed to meet Pyrogen test requirements for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Clean-Cath Intermittent Catheter Recalled by C.R. Bard, Inc. Due to The...
The Issue: The device catheter tip was cut off (no tip) and the product packaging was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slush + Warmer Disc Drape Recalled by Ecolab Inc Due to Slits were...
The Issue: Slits were identified in a low quantity of ORS-320 Slush + Warmer Disc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Cerebro Spinal Fluid Flow Control Valves and Shunts. STRATA...
The Issue: Potential for variation in radiopaque marking visibility under radiographic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic PS Medical Cerebro Spinal Fluid (CSF)-Flow Control Valves for...
The Issue: Potential for variation in radiopaque marking visibility under radiographic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Delta CSF (Cerebro Spinal Fluid) -Flow Control Valves for Recalled...
The Issue: Potential for variation in radiopaque marking visibility under radiographic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WMTS Telemetry Receiver Recalled by Nihon Kohden America Inc Due to...
The Issue: Incorrect Date Stamp or No Data Transfer on Telemetry Receiver and Transmitter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13C-Spirulina Gastric Emptying Breath Test (GEBT) - Product Usage: intended...
The Issue: Potential for false negative diagnosis of gastroparesis. Certain GEBT kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Femoral Sleeves - Product Usage: used primarily in revision...
The Issue: The taper dimensions may be out of specification due to a production issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.