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. 2,471 recalls have been distributed to Utah in the last 12 months.
Showing 22881–22900 of 28,579 recalls
Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Correction due to a fault that causes distal SUJ (DSUJ) failures that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Correction due to a fault that causes distal SUJ (DSUJ) failures that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Master Drug Library Software version 8.0 Recalled by Baxter Healthcare Corp...
The Issue: Loading/Bolus default dose settings in the Master Drug Library and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The FLOW-i Anesthesia System Axillary O2 and Suction Module Recalled by...
The Issue: Maquet has identified that in some FLOW-i Anesthesia System Auxiliary O2 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Steriseal-Cannula Ophthalmic Recalled by Hill-Rom, Inc. Due to The metal...
The Issue: The metal cannula attached to the handpiece can rotate and become dislodged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kinemax Stem Extenders Recalled by Stryker Howmedica Osteonics Corp. Due to...
The Issue: Stryker received four customer complaints reporting that inside the box...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDOPATH ECHELON" Vascular White Reload for Advanced Placement Tip Recalled...
The Issue: During an internal inspection of the production process the firm discovered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziploop Button Product Usage: The Ziploop Button is a non-resorbable...
The Issue: The firm is recalling ToggleLocs and Ziploops manufactured in May and July...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIS27T - Lacrimal Intubation Set RX Only Sterile Used in Recalled by Quest...
The Issue: Expiration date incorrectly printed in Manufacturing Date field on both...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ToggleLoc Recalled by Biomet, Inc. Due to The firm is recalling ToggleLocs...
The Issue: The firm is recalling ToggleLocs and Ziploops manufactured in May and July...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitagel Recalled by Orthovita, Inc., dBA Stryker Orthobiologics. Due to...
The Issue: Several shipments of Vitagel product (a surgical hemostat) required to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASSO NAV Duo Loop eco Catheters Recalled by Biosense Webster, Inc. Due to...
The Issue: Biosense Webster is recalling the LASSO NAV Duo Loop eco Catheters because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captiva's lumbar intervertebral fusion system Reamers (color code rings on...
The Issue: It is possible for the titanium color-coded ring to detach from the Reamers.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Hydrogel Gauze Dressing 2 x 2 Recalled by Amerx Health Care Corp....
The Issue: Nonapproved labeling claims (Sterile)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Tumescent Catheter Inversion (TCI) System. The TCI System...
The Issue: Mislabeled with an incorrect expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 130 Degree Aiming Arm and 125 Degree Aiming Arm Recalled by Synthes,...
The Issue: The guide sleeve has the potential to jam in the Aiming Arms, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Inc. Cardiac Rhythm Disease Management Due...
The Issue: Clinicians observed debris, appearing to originate from the hemostasis valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RECLAIM Assembled Implant Inserter Adaptor orthopedic manual surgical...
The Issue: This lot of the RECLAIM Assembled Implant Inserter Adaptor Instrument may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobius3D Product Usage: Mobius3D software is used for quality assurance...
The Issue: Mobius3D version 1.5.0 contained a defect in software code which affects...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coblator II System Recalled by ArthroCare Medical Corporation Due to The...
The Issue: The recalling firm was notified by the contract manufacturer that they had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.