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. 2,453 recalls have been distributed to Utah in the last 12 months.
Showing 25841–25860 of 28,579 recalls
Recalled Item: OSTEORAPTOR 2.3 mm Suture Anchor with ULTRABRAID COBRAID Suture Recalled by...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX" Ultra 4.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX Ultra 6.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEORAPTOR CURVED 2.3 mm Suture Anchor ULTRABRAID COBRAID Suture Recalled...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEORAPTOR 2.3 mm with 1 ULTRABRAID Suture Recalled by Smith & Nephew, Inc....
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX Ultra HA 4.5 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIORAPTOR 2.9 mm Suture Anchor with DURABRAID" Suture Recalled by Smith &...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPTORMITE" 3.7 mm PLLA with two ULTRABRAID" Sutures Size 0 and Needles...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xario XG Diagnostic Ultrasound System SSA-680A Used for routine diagnostic...
The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xario Diagnostic Ultrasound System SSA-660A Used for routine diagnostic...
The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Scotchcast Recalled by 3M Company - Health Care Business Due to 3M is...
The Issue: 3M is conducting a voluntary product recall of selected lots of 3M"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M ESPE Unitek Primary Stainless Steel Crowns (First Primary UL4) Recalled...
The Issue: 3M ESPE is recalling Unitek Primary Stainless Steel Crowns (First Primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aplio XG Diagnostic Ultrasound System SSA-790A Used for routine diagnostic...
The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aplio MX Diagnostic Ultrasound System SSA-780A Used for routine diagnostic...
The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: nanoPOINT Injector System Recalled by Medicel Ag Due to The...
The Issue: The firm initiated this recall of one lot (121402) of nanoPOINT Injectors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Juno DRF System. Mobile X-ray system These are general Recalled by Villa...
The Issue: It has been discovered that the Air Kerma rate information is inconsistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Soft Tissue Retractor Small Extendible. Offset blade facilitates...
The Issue: The small extendible Soft Tissue Retractor was recalled due to locking nut...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAVIS-EX Recalled by Nidek Inc Due to Under certain circumstances, the Left...
The Issue: Under certain circumstances, the Left eye image may be saved as the Right...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00 4309-049-00 Trabecular Metal Reverse Shoulder Glenosphere Distractor Rx...
The Issue: Zimmer is initiating a lot specific recall of the Trabecular Metal" Reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Tensioning Device The Synthes Osteogenesis System Recalled by...
The Issue: All lots of the Synthes Tensioning Device were recalled due to the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.