State

Utah product recalls

72,940 recalls have nationwide distribution and so reach Utah. 4,901 additional recalls listed Utah specifically in their distribution scope.

What the numbers show

Total: 4,901
Critical: 524
Severe: 1,091
Most recent: 2026-09-09

Of the 4,901 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 1,091 (22%) are Severe.

Which agencies issued them

These figures cover only the 4,901 recalls whose distribution notice names Utah specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3701–3725 of 77841

HighFDA (Devices)·Z-1079-2026·2026-01-21
Azurion interventional systems recalled over nine identified software issues
Philips Medical Systems Nederland is recalling 990 Azurion R3.0 systems over nine identified software issues, including loss of X-ray after a pedal tap and continuous restart.
Product
Philips Azurion Systems R3.0. Includes the following label descriptions and corresponding models: 1. Azurion 3 M12. Model Number: 722229. 2. Azurion 3 M15. Model Number: 722230. 3. Azurion 5 M12. Model Number: 722231. 4. Azurion 5 M20. Model Number: 722232. 5.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1092-2026·2026-01-21
Patient positioning systems recalled over stereotactic radiosurgery tolerance errors
C-RAD Positioning is recalling 189 Catalyst and Catalyst+ systems because the system may indicate a patient as correctly positioned at the isocenter when it is outside tolerance.
Product
Brand Name: Catalyst+ Product Name: Catalyst, Catalyst+ Model/Catalog Number: SP001-0026, SP003-0002 Software Version: cSRS module in combination with cMotion module Product Description: GMDN: 40893 Patient positioning device, diagnostic imaging/radiotherapy, laser Component
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0401-2026·2026-01-21
SMV BodyTrack nuclear medicine systems recalled over a potential detector fall
GE HealthCare is recalling 12 units of the SMV BodyTrack nuclear medicine system, because systems moved without adequate detector support may suffer a detector fall.
Product
Jumbo RAW SHRIMP, All Natural, Chemical Free, No artificial ingredients, NET WT. 32 OZ (2 LB) 907g UPC: 1 93968 00697 6
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0398-2026·2026-01-21
Non-dairy frozen dessert recalled over foreign material in millions of units
WhiteWave is recalling 4,665,608 US units of So Delicious Dairy Free Salted Caramel Cluster Cashewmilk non-dairy frozen dessert over foreign material.
Product
So Delicious Dairy Free Salted Caramel Cluster Cashewmilk, Non-Dairy Frozen Dessert, One Pint (473 mL). UPC 744473 476138. Manufactured By/For So Delicious Dairy Free Eugene, OR 97402 So Delicious Dairy Free Salted Caramel Cluster Cashewmilk, Non-Dairy Frozen Dessert. Net wt. 50
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1100-2026·2026-01-21
Arterial blood sampling kits recalled over a crack on the syringe collar
ICU Medical is recalling 64,290 Pulsator Arterial Blood Sampling Kits because syringes may have a crack on the collar, which may lead to blood leakage and repeated draws.
Product
Pulsator Arterial Blood Sampling Kit, Item Numbers 4044EG-1 4080P-2 4084P-1 4080PE 4080PG
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1093-2026·2026-01-21
Cell wash solution recalled over fungal contamination of an affected lot
Hologic is recalling 3,728 units of ThinPrep CytoLyt Solution over fungal contamination of the affected lot with Parengyodontium album.
Product
ThinPrep¿ CytoLyt¿ Solution. Buffered Cell Wash Solution.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0261-2026·2026-01-21
Frozen raw shrimp recalled over elevated levels of chloramphenicol
AZ Gems is recalling 1,099 cases of Member's Mark Jumbo Raw Shrimp over elevated levels of chloramphenicol.
Product
Advil a) Ibuprofen, Dispenser Pack, 2 tablet packets in box containing 50 individual packets, UPC: 305730154895; b) PM, Ibuprofen, Dispenser Pack, 2 Caplet packets in box containing 50 packets, UPC: 305730164559
Category
Food
Distribution
Distributed nationwide
HighNHTSA·26V029000·2026-01-21
Alexis Fire Equipment Recalls Two Tanker Trucks Due to Loose Fasteners
Alexis Fire Equipment is recalling two tanker trucks (2022 and 2024) because loose axle clamp fasteners may cause a loss of vehicle control.
Product
ALEXIS FIRE EQUIPMENT — ALEXIS FIRE EQUIPMENT FIRE APPARATUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0282-2026·2026-01-21
Carmex lip balm recalled over insanitary conditions at a distribution center
Gold Star Distribution is recalling Carmex over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Product
Carmex a) jar, 12 count, UPC: 083078123154, 083078113155; b) Tube, PEG, 12 count, UPC: 083078123147, 083078113148
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0262-2026·2026-01-21
Aleve recalled over insanitary conditions at a distribution center
Gold Star Distribution is recalling Aleve over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Product
Aleve 1's, 60 CT
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1095-2026·2026-01-21
Coagulation reagent recalled over potential for microbial contamination
Instrumentation Laboratory is recalling 7,720 units of a coagulation reagent used for evaluating the intrinsic pathway and monitoring heparin therapy over potential microbial contamination.
Product
The product is used for the evaluation of the intrinsic coagulation pathway, APTT substitution test and the monitoring of heparin therapy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1099-2026·2026-01-21
Circulatory support blood pumps recalled over locking into the motor
Thoratec is recalling 8,399 CentriMag blood pump products after reports that the pump may not fit or lock securely into the motor using the screw-in locking feature.
Product
CentriMag Blood Pump, REF: 102953, 201-20003, 201-90010, 201-90016; CentriMag RVAD HDE KIT, REF: 104318; CentriMag Pre-connected Pack, REF: CMAEK00; CentriMag VAD KIT, REF: 201-51006, 201-51007, 201-90001 201-90001T; Blood Pump with CentriMag Acute Circulatory Support System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0269-2026·2026-01-21
Excedrin recalled over insanitary conditions at a distribution center
Gold Star Distribution is recalling Excedrin over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Product
EXCEDRIN 2'S DISP.- 30 CT
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0271-2026·2026-01-21
Nuclear medicine systems recalled over inadequate detector support during transport
GE Medical Systems Israel is recalling 38 MAXXUS systems because units past end of guaranteed service may have been moved without adequate detector support, risking a detector fall.
Product
MOTRIN 2'S DISP.- 50CT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0263-2026·2026-01-21
Alka Seltzer recalled over insanitary conditions at a distribution center
Gold Star Distribution is recalling Alka Seltzer over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Product
Alka Seltzer, a) Original, 2 tablets per packet in 58 count box, UPC: 815556020033, 016500514473, b) Plus Cold & Flu, 2 tablets per packet in 36 count box, UPC: 016500594932
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0265-2026·2026-01-21
Bayer aspirin recalled over insanitary conditions at a distribution center
Gold Star Distribution is recalling Bayer 2Pk over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Product
Bayer 2Pk- 25 CT
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0279-2026·2026-01-21
TUMS antacid tablets recalled over insanitary conditions at a distribution center
Gold Star Distribution is recalling TUMS antacid tablets over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Product
TUMS a) Assorted, 12 Ct.; b) Extra Strength (EX) Assorted Berries, 12-count #1194A *05/27; c)Extra Strength (EX) Assorted Fruit, 12-count, #1194C *03/27
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1087-2026·2026-01-21
PALACOS MV bone cement recalled because ampoules may not break
Heraeus Medical is recalling PALACOS MV pro 40 and PALACOS MV pro 80 bone cement because an unfortunate combination of factors can leave ampoules unbroken, so no appropriate cement dough is formed.
Product
Medline medical procedure convenience kits labeled as: 1) WCH BARI-GASTRECTOMY CDS, REF CDS860237AF; 2) ROBOTIC PROCEDURE, REF CDS982128Q; 3) CUH THORACIC, REF CDS984338M; 4) THORACIC PROCEDURE, REF CDS984640I; 5) DAVINCI ROBOTIC PACK-LF, REF DYNJ0525321O; 6) LAP CHO
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1090-2026·2026-01-21
Robotic prostate kits recalled over suction irrigators that can leak
Medline is recalling 12 units of procedure convenience kits containing Stryker Strykeflow 2 Suction Irrigators, which can leak or emit vaporized saline during use.
Product
Medline medical procedure convenience kits labeled as: KIT ROBOTICS UROLOGY PROSTATE, REF DYKMBNDL116G
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1053-2026·2026-01-21
Donor nephrectomy accessory kits recalled over recalled B. Braun sets
Medline is recalling 33 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: RR-LAP DONOR NEP ACCESSORY, Medline kit SKU DYNJ63395B
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1056-2026·2026-01-21
IV start kits recalled over recalled B. Braun administration sets inside
Medline is recalling 5314 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) IV START KIT NS, Medline kit SKU DYKM1980C; 2) (134) L&D IV-START SET, Medline kit SKU DYKM2137B; 3) IV START KIT, Medline kit SKU DYKS1372C; 4) IV START KIT, Medline kit
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1074-2026·2026-01-21
Allura Xper FD10/10 systems recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 22 units of the Allura Xper FD10/10, model 722027, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD10/10; Model Number: 722027;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1063-2026·2026-01-21
Allura Xper FD10F systems recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 12 units of the Allura Xper FD10F, model 722002, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD10F; Model Number: 722002;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1050-2026·2026-01-21
Open heart kits recalled because they contain recalled B. Braun administration sets
Medline is recalling 633 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) OPEN HEART ACCESSORY CDSKit SKU CDS984289O; 2) OPEN HEART CDSKit SKU CDS984355K; 3) BAG A OPEN HEART KITKit SKU DYKM1025D; 4) RR-CABG SUPPLEMENTAL PACKKit SKU DYNJ0394752
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0274-2026·2026-01-21
Admission and admin kits recalled over recalled B. Braun administration sets
Medline is recalling 1725 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Product
CHILDREN NYQUIL, COLD&FLU, BERRY, 8oz, 12ct
Category
Medical Device
Distribution
Distributed nationwide