- Home
- Utah Recalls
Utah Recalls
3,498 recalls on record affecting Utah
SDI Limited recalls Dentsply Sirona Capsule Mixer Model No. 5546068
Potential for electrical discharge from unit when unplugged.
View recall details →
Bard Access Systems, Inc. recalls BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK
After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically necessary cases, users may experience difficulty/inability to remove obturator, due to it locking to the needle hub, due to out-of-tolerance dimensions and IFU unclarity, which may result in new needle placement, which may result in delayed therapy
View recall details →
529 COMMERCE, LLC recalls Aquafaba Powder, Vegan Replacement, NET WT. 4 oz (113g) and
Undeclared Egg
View recall details →
Prospector Popcorn, LLC recalls Prospector Popcorn Belgian Chocolate Toffee Gourmet Popcorn
Inaccurately declared nutrients including Iron (understated), and Vitamin D (overstated).
View recall details →
Prospector Popcorn, LLC recalls Prospector Popcorn Chocolate Mocha Gourmet Popcorn 1.5 oz.
Inaccurately declared nutrients including Carbohydrates (understated) and Cholesterol (understated).
View recall details →
Prospector Popcorn, LLC recalls Prospector Popcorn Maple Walnut Ice Cream Gourmet Popcorn 3.
Inaccurately declared nutrients including Potassium (overstated), Calcium (overstated), and Iron (understated).
View recall details →
Prospector Popcorn, LLC recalls Prospector Popcorn Fudge Brownie Gourmet Popcorn 1.5oz and 3
Inaccurately declared nutrients including Potassium (overstated) and Calcium (overstated).
View recall details →
Byron White Formulas, Inc. recalls Byron White FORMULAS A-L Complex Herbal Supplement 1.0 fl. o
Label does not declare walnuts in English
View recall details →
Dreyer's Grand Ice Cream Inc. recalls Outshine Fruit Bars Tangerine, 6-Count 2.5 ounce, with UPC 0
Foreign object: products may contain glass pieces
View recall details →
Byron White Formulas, Inc. recalls Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL
Label does not declare walnuts in English
View recall details →
Dreyer's Grand Ice Cream Inc. recalls Outshine Fruit Bars Strawberry, Pineapple, Grape, Tangerine.
Foreign object: products may contain glass pieces
View recall details →
Dreyer's Grand Ice Cream Inc. recalls Outshine Fruit Bars Black Cherry, 6 Bars, 2.5 ounce, with UP
Foreign object: products may contain glass pieces
View recall details →
Dreyer's Grand Ice Cream Inc. recalls Outshine Fruit Bars Strawberry, 6-Count 2.5 ounce, with UPC
Foreign object: products may contain glass pieces
View recall details →
Dreyer's Grand Ice Cream Inc. recalls Outshine Fruit Bars Grape, 6-Count 2.5 ounce, with UPC 04154
Foreign object: products may contain glass pieces
View recall details →
Dreyer's Grand Ice Cream Inc. recalls Outshine Fruit Bar Watermelon, 6-Count 2.5 ounce with UPC 04
Foreign object: products may contain glass pieces
View recall details →
Byron White Formulas, Inc. recalls Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30
Label does not declare walnuts in English
View recall details →
BD SWITZERLAND SARL recalls 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI cod
Products may not have received adequate sterilization processing.
View recall details →
Argon Medical Devices, Inc recalls L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga
Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking and/or cracking at the hub, which may lead to replacement, inability to flush/aspirate catheter, catheter occlusion, therapy interruption, blood loss, tissue irritation, bloodstream infection.
View recall details →
Argon Medical Devices, Inc recalls L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 38462
Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking and/or cracking at the hub, which may lead to replacement, inability to flush/aspirate catheter, catheter occlusion, therapy interruption, blood loss, tissue irritation, bloodstream infection.
View recall details →
Orthofix U.S. LLC recalls Orthofix MINIRAIL, SHORT, LENGTHENER REF: M103, Unilateral
Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111
View recall details →
Showing 20 of 3,498 recalls. Use search to filter further.