State

Mississippi product recalls

72,940 recalls have nationwide distribution and so reach Mississippi. 5,349 additional recalls listed Mississippi specifically in their distribution scope.

What the numbers show

Total: 5,349
Critical: 923
Severe: 1,126
Most recent: 2026-09-09

Of the 5,349 recalls naming Mississippi we have scored against our rubric, 923 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,126 (21%) are Severe.

Which agencies issued them

These figures cover only the 5,349 recalls whose distribution notice names Mississippi 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 78289

HighFDA (Drugs)·D-0286-2026·2026-01-21
Deodorant products recalled over insanitary conditions at a distribution center
Gold Star Distribution is recalling Deodorant products over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Product
Deodorant: a) Axe, Body Spray, Wild Spice, 6CT, 150ML, UPC: 600108736469; b) LUCKY MENS STICK DEODORANT, SPRING FRESH, 24CT, 2.5 OZ, UPC: 808829111668; c) LUCKY MENS STICK DEODORANT, FRESH COMFORT, 24CT, 1.6 OZ, UPC: 808829089103; d) LADY DEODORANT, CHERRY BLOSSOSM, 24CT, 1.8oz,
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1057-2026·2026-01-21
Levothyroxine tablets recalled after a bottle held the wrong strength
Alvogen is recalling a lot of Levothyroxine Sodium Tablets, 150mcg, after a pharmacy reported a single bottle containing 88 mcg tablets instead of 150 mcg tablets.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) PRE OP KIT, Medline kit SKU DYKS1093B; 2) PRE OP KIT, Medline kit SKU DYKS1124C; 3) PRE OP KIT, Medline kit SKU DYKS1128C; 4) PREOP KIT, Medline kit SKU DYKS1130B; 5) P
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 (Drugs)·D-0270-2026·2026-01-21
Excedrin Migraine recalled over insanitary conditions at a distribution center
Gold Star Distribution is recalling Excedrin Migraine over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Product
EXCEDRIN MIGRAINE 2'S- 25 CT
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1084-2026·2026-01-21
Lucky Ice mouthwash recalled over insanitary conditions at a distribution center
Gold Star Distribution is recalling Lucky Ice Cool Mouthwash over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Product
Asserachrom HPIA. Model/Catalog Number: 00615. The Asserachrom HPIA kit is intended for the qualitative detection in plasma or serum of the anti-heparin-platelet factor 4 (PF4) antibodies generated during the type II heparin-induced thrombocytopenia (HIT type II) by ELISA.
Category
Drug
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-0287-2026·2026-01-21
Ground cinnamon recalled over elevated levels of lead
Eureka Inc is recalling 32 cases of ground cinnamon in 100g clear plastic containers over elevated levels of lead.
Product
Toothpaste: a) COLGATE, TOOTHPASTE, WHITENING, 2.5oz, 24ct; UPC: 035000511065; b) COLGATE, TOOTHPASTE, Regular, 2.5oz, 24ct, UPC: 035000511058; c) COLGATE, TOOTHPASTE, TRIPLE, 2.5oz, 24ct, UPC: 035000512109; d) COLGATE, TOOTHPASTE, MINT ZING, 24CT, 2.5oz, UPC: 035000744609; COLGA
Category
Food
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-0281-2026·2026-01-21
Ice gel recalled over insanitary conditions at a distribution center
Gold Star Distribution is recalling Personal Care Ice Gel over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Product
Personal Care, Ice Gel, 8oz, 12 count, UPC 048155903463
Category
Drug
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 (Drugs)·D-0264-2026·2026-01-21
Benadryl tablets recalled over insanitary conditions at a distribution center
Gold Star Distribution is recalling Benadryl over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Product
Benadryl, 25'S 2PK Box, UPC 815556020316
Category
Drug
Distribution
Distributed nationwide
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-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 (Devices)·Z-1042-2026·2026-01-21
Angioplasty balloon catheters recalled over inflation and deflation difficulty
Boston Scientific is recalling 21 Coyote over-the-wire PTA balloon dilatation catheters over the potential for inflation and deflation difficulty during use in the peripheral vasculature.
Product
Boston Scientific Coyote OVER-THE-WIRE PTA Balloon Dilation Catheter, 4F, 1) 2.5mm x120mm, 150 cm, UPM/Model No. REF H74939186251210; 2) 3.5mm x120mm, 150 cm, UPM/Model No. REF H74939186351210; Catheter, Angioplasty, Peripheral, Transluminal
Category
Medical Device
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-1071-2026·2026-01-21
MRI systems recalled over ice that may block the magnet venting system
Canon Medical Systems is recalling 34 Vantage Galan 3T MRI systems because ice may form in the venting system, and a quench in that condition could rupture the helium vessel.
Product
Allura Xper FD20 Biplane; Model Number: 722013;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0278-2026·2026-01-21
Halls cough drops recalled over insanitary conditions at a distribution center
Gold Star Distribution is recalling Halls Cough Drops across multiple flavours over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Product
Halls Cough Drops a) BAGS, MENTHOL, 12CT; b) BAGS, HONEY LEM, 12CT; c) BAGS, DEFENSE CITRUS, 12CT; d) BAGS, CHERRY, 12CT; e) M. CHERRY, 20 STK; f) BRAZIL, Cherry, 21CT/27.5G; f) LEMON. HONEY, 20CT #1180E; g) LIME FRESH, 20CT, #1182; h) MENTHOL BLUE, 20CT, #1180A; i) BRAZIL, Menth
Category
Drug
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 (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
ModerateFDA (Devices)·Z-1077-2026·2026-01-21
Allura Xper FD20/20 systems recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 8 units of the Allura Xper FD20/20, model 722038, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD20/20; Model Number: 722038;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1059-2026·2026-01-21
Neuro angio packs recalled over recalled B. Braun administration sets inside
Medline is recalling 12 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: NEURO ANGIO PACK, Medline kit SKU DYNJ38935
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1043-2026·2026-01-21
Neurostimulator clinician programmer app recalled over faults during device use
Medtronic is recalling 7,123 units of the Vanta Clinician Programmer Application after complaints that it does not function as intended during use.
Product
A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683, Product number A71200. Software is deployed and operated on Samsung tablets (CFN CT900).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1091-2026·2026-01-21
Azurion systems recalled over six identified software issues
Philips Medical Systems Nederland is recalling 10,466 Azurion systems on software versions R2.1.10 and R2.2.10 over six identified software issues including continuous restart.
Product
Philips Azurion Systems with software versions R2.1.10 and R2.2.10. Includes the following label descriptions and corresponding models: 1. Azurion 3 M12. Model Numbers: 722063, 722221. 2. Azurion 3 M15. Model Numbers: 722064, 722222, 722280. 3. Azurion 5 M12. Model Num
Category
Medical Device
Distribution
Distributed nationwide