State

Utah product recalls

73,738 recalls have nationwide distribution and so reach Utah. 4,914 additional recalls listed Utah specifically in their distribution scope.

What the numbers show

Total: 4,914
Critical: 524
Severe: 1,350
Most recent: 2026-10-28

Of the 4,914 recalls naming Utah we have scored against our rubric, 524 (11%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,350 (27%) are Severe.

Which agencies issued them

These figures cover only the 4,914 recalls whose distribution notice names Utah specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31851–31875 of 78652

HighFDA (Devices)·Z-1276-2020·2020-02-26
FDA Recalls Polysorb Sutures Due to Packaging Integrity Concerns
The FDA is recalling specific lots of Polysorb Braided Absorbable Sutures due to potential packaging integrity issues that could compromise sterility.
Product
Polysorb Braided Absorbable Suture 2/0 30 VIOLET GS-21, Item Code CL811 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1305-2020·2020-02-26
Nobel Biocare Recalls Screw Taps Due to Packaging Seal Defects
Nobel Biocare is recalling Screw Tap Tapered WP Single-Pat devices because a packaging sealing defect may compromise sterility during shelf life.
Product
Screw Tap Tapered WP Single-Pat - Product Usage: The Guided Drills (Twist (Step) Drills, Guided Tapered Drills) are used for preparing osteotomies for the specific related implants.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1331-2020·2020-02-26
Siemens Luminos dRF Max Recalled for Collision Control Override Risk
Siemens is recalling 46 Luminos dRF Max devices because an override function can disable collision controls, creating a risk of collision with obstacles or persons.
Product
Luminos dRF Max, Model No. 10762471 - Product Usage: Luminos dRF Max is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image. The system has medical applications ranging from gastrointestinal examinations to cranial, skeletal…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1310-2020·2020-02-26
Nobel Biocare Tapered Drills Recalled Due to Sterility Concerns
Nobel Biocare is recalling 154 units of Tapered RP 4.3x13 mm drills because a packaging defect may compromise sterility.
Product
Drill Tapered RP 4.3x13 mm Single-Pat - Product Usage: The Guided Drills (Twist (Step) Drills, Guided Tapered Drills) are used for preparing osteotomies for the specific related implants.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1298-2020·2020-02-26
Polysorb Braided Absorbable Suture Recalled for Packaging Integrity Issues
Covidien LLC is recalling specific lots of Polysorb Braided Absorbable Suture due to potential packaging integrity issues that may impact the humidity or sterility barrier.
Product
Polysorb Braided Absorbable Suture 0 30" VIOLET GU-46, Item Code UL877 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1318-2020·2020-02-26
Nobel Biocare Implant Retrieval Instrument Recall Due to Sterility Concerns
Nobel Biocare is recalling 31 units of Implant Retrieval Instrument CC 3.0 31 mm because a packaging sealing defect may compromise sterility.
Product
Implant Retrieval Instrument CC 3.0 31 mm- Product Usage: They can be used to remove implants, if the implant connection has been damaged. It can be used to remove implants with internal conical connection, internal tri-channel connection or external hex connection.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0728-2020·2020-02-26
CSM Bakery Products Recalls Vanilla Buttercreme Frosting Due to Plastic Contamination
CSM Bakery Products is recalling 35 lb. pails of Vanilla Xtra Smooth Buttercreme Frosting because pieces of plastic polymer were introduced into the sugar system.
Product
35 lb. pail VANILLA XTRA SMOOTH BUTTERCREME FROSTING, MDM # 10203023, Manufactured by Brill Inc. Tucker, GA 30084 1 866 982 7455 OR BRILLINC.COM
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1322-2020·2020-02-26
Nobel Biocare Abutment Screw Retrieval Instruments Recalled for Sterility Concerns
Nobel Biocare is recalling 233 units of Abutment Screw Retrieval Instruments because a packaging defect may compromise sterility during shelf life.
Product
Abutment Screw Retrieval Instrument 3.0/NP - Product Usage: The instruments for abutment screw retrieval can be used if an abutment screw is broken and a part of the screw is left inside the implant screw channel. If the implant thread needs to be cleaned before placing a new…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1273-2020·2020-02-26
Smith & Nephew Recalls TwinFix Ti Suture Anchors Due to Sterility Risk
Smith & Nephew is recalling TwinFix Ti 2.8 mm HS Suture Anchors because a protective tube failure may have breached the sterile barrier.
Product
TwinFix Ti 2.8 mm HS Suture Anchor - Product Usage: A fixation device intended to provide secure attachment of soft tissue to bone.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1340-2020·2020-02-26
Siemens ARTIS Pheno-Interventional Fluoroscopic X-Ray System Recalled for Robotic Stand Defect
Siemens Medical Solutions is recalling 96 ARTIS Pheno-Interventional Fluoroscopic X-Ray Systems because safety brakes may block the robotic stand, preventing intended movements.
Product
ARTIS Pheno-Interventional Fluoroscopic X-Ray System Model Number: 10849000 - Product Usage:AXIOM Artis is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1306-2020·2020-02-26
Nobel Biocare Tapered Drills Recalled Due to Sterility Concerns
Nobel Biocare is recalling specific tapered dental drills because a packaging defect may compromise their sterility during shelf life.
Product
Drill Tapered NP 3.5x10 mm Single-Pat - Product Usage: The Guided Drills (Twist (Step) Drills, Guided Tapered Drills) are used for preparing osteotomies for the specific related implants.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0721-2020·2020-02-26
CSM Bakery Recalls Frozen Cookie Dough Due to Plastic Contamination
CSM Bakery Products is recalling frozen chocolate chip cookie dough because pieces of plastic polymer were introduced into the sugar system.
Product
30 lb. cases of 480 1.0 oz frozen chocolate chip with mini colored candy pieces cookie dough, MDM # 10194626, Manufactured by Brill Inc. Tucker, GA 30084 1 866 982 7455 OR BRILLINC.COM
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0849-2020·2020-02-26
American Health Packaging Recalls Desmopressin Acetate Tablets Due to Missing Desiccant
American Health Packaging is recalling Desmopressin Acetate Tablets because product bottles may be missing desiccant.
Product
Desmopressin Acetate Tablets, 0.2 mg, 30 tablets (3 x 10 unit dose blister cards), Rx Only, Packaged and distributed by: American Health Packaging, Columbus, Ohio 43217. NDC Carton: 68084-604-21; NDC Unit Dose 68084-604-11
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1283-2020·2020-02-26
FDA Recalls Polysorb Sutures Due to Packaging Integrity Concerns
The FDA is recalling specific lots of Polysorb Braided Absorbable Sutures due to potential packaging integrity issues that could compromise the sterility barrier.
Product
Polysorb Braided Absorbable Suture 2-0 VIOLET 36" GS-21, Item Code CL923 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1309-2020·2020-02-26
Nobel Biocare Recalls Tapered Dental Drills Due to Sterility Concerns
Nobel Biocare is recalling 260 units of tapered dental drills because a packaging sealing issue may compromise sterility during shelf life.
Product
Drill Tapered RP 4.3x11.5 mm Single-Pat - Product Usage: The Guided Drills (Twist (Step) Drills, Guided Tapered Drills) are used for preparing osteotomies for the specific related implants.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1295-2020·2020-02-26
FDA Recalls Polysorb Sutures Due to Potential Packaging Integrity Issues
The FDA is recalling specific lots of Polysorb Braided Absorbable Sutures due to potential packaging integrity issues that could impact the humidity or sterility barrier.
Product
Polysorb Braided Absorbable Suture UD 4/0 18 P-13, Item Code SL5690 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1323-2020·2020-02-26
Nobel Biocare Recalls Implant Retrieval Kits Due to Sterility Concerns
Nobel Biocare is recalling 87 units of Implant Retrieval Kits because a packaging sealing issue may compromise the sterility of the devices during their shelf-life.
Product
Implant Retrieval Kit - Product Usage: The kit itself does not have a specific intended Use, but included devices have specific intended use as shown above.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1257-2020·2020-02-26
Ormco/Sybronendo Recalls SnapLink Brackets Due to Slide Door Failure
Ormco/Sybronendo is recalling SnapLink brackets because the lower buccal tube slide doors may not stay closed, potentially causing tooth rotation and treatment delays.
Product
SnapLink, Ref Part No. 438-2190, L6R SnapLink, Slot .022, TQ--28, Ang +2, Rot +2, Qty 10, Made in Mexico, CE 0086, Rx Only
Category
Medical Device
Distribution
51 states
ModerateFDA (Devices)·Z-1263-2020·2020-02-26
Abbott i-STAT CG4+ Cartridges Recalled for Lack of FDA Clearance
Abbott Point Of Care Inc. is recalling i-STAT CG4+ cartridges because they are not FDA cleared and lack CLIA waived status.
Product
i-STAT CG4+ cartridge (blue), List No. 03P85-50. UDI (01) 00054749002269 - Product Usage: The i-STAT CG4+ cartridge is intended for the quantitative measurement of lactate, pH, pCO2, and pO2 in venous, arterial or capillary whole blood.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1296-2020·2020-02-26
Polysorb Braided Absorbable Suture Recalled for Packaging Integrity Issues
Covidien LLC is recalling Polysorb Braided Absorbable Sutures due to potential packaging integrity issues that may impact the humidity or sterility barrier.
Product
Polysorb Braided Absorbable Suture 4/0 30 VIO SC-2 124K, Item Code SL654 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0848-2020·2020-02-26
American Health Packaging Recalls Desmopressin Acetate Tablets Due to Missing Desiccant
American Health Packaging is recalling Desmopressin Acetate Tablets because the product bottles may be missing desiccant.
Product
Desmopressin Acetate Tablets, 0.1 mg, 30 tablets (3 x 10 unit dose blister cards), Rx Only, Packaged and distributed by: American Health Packaging, Columbus, Ohio 43217. NDC Carton: 68084-606-21; NDC Unit Dose 68084-606-11
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1262-2020·2020-02-26
Abbott i-STAT CHEM8+ Cartridges Recalled for Lack of FDA Clearance
Abbott Point Of Care Inc. is recalling i-STAT CHEM8+ cartridges because they are not FDA cleared and do not have CLIA waived status.
Product
i-STAT CHEM8+ cartridges (blue), List No. 09P31-25. UDI (01) 00054749001910 - Product Usage: The i-STAT CHEM8+ cartridge may be used for the quantitative measurement of sodium, potassium, chloride, blood urea nitrogen (BUN), ionized calcium, TCO2, glucose, creatinine, and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1248-2020·2020-02-26
Arrow Epidural Catheterization Kit Recalled for Incorrect Expiration Date
Arrow International Inc. is recalling 1,320 units of the Arrow Epidural Catheterization Kit because the product lidstock contains the incorrect expiration date.
Product
Arrow EPIDURAL CATHETERIZATION KIT AM-05500
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1249-2020·2020-02-26
Arrow Epidural Catheterization Kit Recalled for Incorrect Expiration Date
Arrow International Inc. is recalling 1,360 units of the Arrow Epidural Catheterization Kit CK-02220 because the product lidstock contains the incorrect expiration date.
Product
Arrow EPIDURAL CATHETERIZATION KIT CK-02220
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1316-2020·2020-02-26
Nobel Biocare Implant Retrieval Instruments Recalled for Sterility Concerns
Nobel Biocare is recalling 2,470 implant retrieval instruments because a packaging defect may compromise sterility. The devices are distributed worldwide.
Product
Implant Retrieval Instrument Hex & Tri-Ch NP/RP 22mm - Product Usage: They can be used to remove implants, if the implant connection has been damaged. It can be used to remove implants with internal conical connection, internal tri-channel connection or external hex connection.
Category
Medical Device
Distribution
Distributed nationwide