State

Alabama product recalls

73,576 recalls have nationwide distribution and so reach Alabama. 6,372 additional recalls listed Alabama specifically in their distribution scope.

What the numbers show

Total: 6,372
Critical: 1,131
Severe: 1,602
Most recent: 2026-10-14

Of the 6,372 recalls naming Alabama we have scored against our rubric, 1,131 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,602 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,372 recalls whose distribution notice names Alabama specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

126–150 of 79948

SevereFDA (Devices)·Z-0119-2027·2026-10-14
Intellijoint Navigation Systems Recalled for Potential Fire Risk
Intellijoint Surgical is recalling eight navigation systems because their workstations may contain a defective Apple battery that could overheat and cause a fire.
Product
Intellijoint Navigation System: Workstation G2 Configured, REF: 000-0241; Intellijoint HIP Cart System, REF: 000-0250; Intellijoint HIP, Portable System, REF: 000-0249
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0075-2027·2026-10-14
Steris VERIFY Biological Steam Test Pack Recalled for Spore Population Defect
Steris Corporation is recalling VERIFY Biological Steam Test Packs because the spore population may fall below specifications, potentially causing false-negative steam sterilization results.
Product
VERIFY Biological Steam Test Pack Model/Catalog Number: S3069
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0032-2027·2026-10-14
FDA Recalls Tri-MIX Syringes Due to Sterility Assurance Concerns
Carolina Infusion, LLC is recalling Tri-MIX compounded syringes due to a lack of assurance of sterility related to formulation and processing equipment.
Product
Tri-MIX (PAPAV/PHENTO/ALPROS),30/2/40, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0072-2027·2026-10-14
Steris VERIFY Biological Indicator Recall Due to Spore Population Concerns
Steris is recalling VERIFY Dual Species Self-Contained Biological Indicators because spore populations may fall below specifications, potentially leading to false sterilization results.
Product
VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3060
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0004-2027·2026-10-14
K.C. Pharmaceuticals Recalls Leader Advanced Relief Eye Drops for Sterility Concerns
K.C. Pharmaceuticals is recalling Leader Advanced Relief Eye Drops and related brands due to a lack of assurance of sterility. The recall covers 208,896 cartons distributed nationwide.
Product
LEADER ADVANCED RELIEF EYE DROPS — LEADER ADVANCED RELIEF EYE DROPS (DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0037-2027·2026-10-14
Apothecary NAD+ Injection Recalled for Lack of Sterility Assurance
Apothecary Pharma is recalling NAD+ Injection vials due to a lack of assurance of sterility. The product was distributed nationwide.
Product
Apothecary NAD+ Injection 200 mg/mL, 6 mL Sterile Multi-Dose Vial, Rx Only, Apothecary Pharma, LLC, 1913 Evans Road, Cary, NC, 27513, NDC 85091-011-06.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0108-2027·2026-10-14
Canon Medical Alphenix INFX-8000C/B5 Recalled for Tabletop Shift Risk
Canon Medical System is recalling one Alphenix INFX-8000C/B5 unit in Idaho due to a risk of tabletop shifting that could cause patient misalignment.
Product
Alphenix INFX-8000C/B5
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V673000·2026-10-14
Toyota Recalls Land Cruiser Hybrid Vehicles for Fuel Leak Risk
Toyota is recalling 2024-2027 Land Cruiser Hybrid vehicles because a fuel tube connection may disconnect and leak fuel, increasing fire risk.
Product
TOYOTA — TOYOTA LAND CRUISER HYBRID
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·H-0011-2027·2026-10-14
Better Bakehouse Recalls Donutful Chocolate Dipped Vanilla Cake Donuts for Undeclared Milk
The Better Bakehouse Snack Company is recalling Donutful Chocolate Dipped Vanilla Cake Donuts due to undeclared milk. The product was distributed nationwide.
Product
Donutful Chocolate Dipped Vanilla Cake Donuts - 7.05oz/10ct.Case Configuration 5 count carton, 6 cartons per case. UPC 850041392103. Paperboard carton containing 5 individually wrapped packages of two donuts each. UPC: 850041392103. The Better Bakehouse Snack Co. 3651 Lindell…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·H-0020-2027·2026-10-14
Sweet Sensi THC Gum Drops Recalled for Staphylococcus aureus
Sweet Sensi is recalling Passion Guava Kush THC gum drops nationwide due to the detection of Staphylococcus aureus.
Product
Sweet Sensi Elevated Edibles Hybrid Gum Drops - Passion Guava Kush 140mg THC. Product is packaged in sealable & flexible gold, purple and black metallic plastic mylar pouch and is sold in two sizes: 1) Net wt. Approx. 2.1oz (60g) 10 count and 2) Net wt. 6.3oz (180g) 30 count.…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0070-2027·2026-10-14
Steris VERIFY Biological/Integrator Challenge Pack Recall for Sterilization Monitoring Failure
Steris Corporation is recalling VERIFY Biological/Integrator Challenge Packs because the spore population may be too low to accurately monitor steam sterilization cycles.
Product
VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB006
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0029-2027·2026-10-14
FDA Recalls Tirzepatide/Cyanocobalamin Injectable Due to Sterility Concerns
Carolina Infusion, LLC is recalling Tirzepatide/Cyanocobalamin 76/2 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.
Product
TIRZEPATIDE/CYANOCOBALAMIN 76/2 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0005-2027·2026-10-14
K.C. Pharmaceuticals Recalls Target Eye Drops for Sterility Concerns
K.C. Pharmaceuticals is recalling multiple brands of eye drops due to a lack of assurance of sterility. The recall covers 1,435,830 cartons distributed nationwide.
Product
TARGET EYE DROPS MAXIMUM REDNESS RELIEF EYE — TARGET EYE DROPS MAXIMUM REDNESS RELIEF EYE (GLYCERIN, NAPHAZOLINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-0014-2027·2026-10-14
GIAS Food Inc. Recalls Lemon Alfredo Fettuccine for Listeria Contamination
GIAS Food Inc. is recalling 1,174 cases of Lemon Alfredo Fettuccine due to contamination with Listeria monocytogenes. The product was distributed to retail locations nationwide.
Product
Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with pink and black lettering; label reads in part as "bettergoods Lemon Alfredo Fettuccine, MADE IN ITALY, NET WT 22 OZ, BEST if Used By: SEP 21 2027 L6081A, UPC 194346442706, DISTRIBUTED BY: Walmart Inc.…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0107-2027·2026-10-14
Polymedco Sediplast Tubes Recalled for Potential Blood Exposure
Polymedco is recalling Sediplast tubes because pressure buildup may eject the cap, releasing blood and creating a biological hazard for operators.
Product
SEDIPLAST; Model/Catalog Numbers: S-100 and S-1000;
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0023-2027·2026-10-14
FDA Recalls Tri-MIX Injectable Due to Sterility Concerns
Carolina Infusion, LLC is recalling Tri-MIX injectable syringes due to a lack of assurance of sterility related to processing equipment.
Product
Tri-MIX (PAPAV/PHENTO/ALPROS),30/1/10, injectable, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936,
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0085-2027·2026-10-14
Stryker Bard EP XT Decapolar Steerable Diagnostic EP Catheter Recalled for Sterile Barrier Breach
Stryker is recalling Bard EP XT Decapolar Steerable Diagnostic EP Catheters due to a potential sterile barrier breach that could lead to particulate embolization, infection, or thrombus formation.
Product
BARD EP XT DECAPOLAR STEERABLE, DIAGNOSTIC EP CATHETER, 6F, LARGE 4.0, 10, 2-5-2MM, REF: 201007
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0017-2027·2026-10-14
biQ-FEL Beverage Recalled for Undeclared Sildenafil and Tadalafil
A&P CREATIONS is recalling biQ-FEL beverage bottles containing undeclared Sildenafil and Tadalafil. The product was distributed nationwide.
Product
biQ-FEL, 16.9 fl oz (500 mL), 17 servings per bottle, Manufactured by ALMENAT SAS AV 39 OESTE No 10 OESTE-18 CALI VALLE INDUSTRIA COLOMBIANA; Distributed by: Biofel
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0031-2027·2026-10-14
Carolina Infusion Recalls Tri-MIX Injectable Due to Sterility Concerns
Carolina Infusion, LLC is recalling Tri-MIX injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.
Product
Tri-MIX (PAPAV/PHENTO/ALPROS),30/2/20, injectable, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0021-2027·2026-10-14
FDA recalls injectable compounded mixture in single-use syringes
Carolina Infusion LLC is recalling QUAD-MIX injectable compounded product nationwide due to sterility concerns.
Product
QUAD-MIX( PAPAV/PHENTO/ALPROS/TROP) INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0078-2027·2026-10-14
Philips Spectral CT Systems Recalled for Software Issues Affecting Safety
Philips Medical Systems is recalling 539 Spectral CT systems due to software issues that may cause image artifacts, wrong slice thickness, or unintended system motion.
Product
Spectral CT and Spectral CT 7500 RT; Software Version Numbers: 5.2.X (U.S.); 5.0.X, 5.2.X, 5.4.X (Outside U.S.); Model Numbers: 1. 728333 (U.S. and Outside U.S.), 2. 728340 (Outside U.S.), 3. 728344 (Outside U.S.), 4. 728345 (Outside U.S.);
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V674000·2026-10-14
PACCAR Recalls 2027 Kenworth and Peterbilt Trucks for Bunk Restraint Defect
PACCAR is recalling 310 model-year 2027 Kenworth and Peterbilt trucks because improperly secured sleeper bunk webbing may fail to restrain occupants during a crash.
Product
KENWORTH — KENWORTH, PETERBILT T680, W900, 579, 589
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0073-2027·2026-10-14
Steris VERIFY Dual Species Biological Indicator Recall for Spore Population Issues
Steris Corporation is recalling VERIFY Dual Species Self-Contained Biological Indicators because the spore population may fall below specifications, potentially leading to false sterilization results.
Product
VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3061
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·N/A·2026-10-14
Beak & Skiff Alcohol Antiseptic Sanitizer recalled for acetaldehyde contamination
Beak & Skiff Sanitizer Alcohol Antiseptic 80% is being recalled because FDA analysis found acetaldehyde above specification limits in the product. The recall affects bottles distributed in New York and through online sales.
Product
Tri-Immune Boost (Glutathione: 200 mg, Ascorbic Acid: 200 mg, Zinc: 2.5 mg), 30 mL vial, Rx only, Centric Compounding, 7447 Harwin Dr. Suite 111, Houston, TX 77036
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0101-2027·2026-10-14
Avid Medical Recalls 30 DAVINCI LAP/GYN Kits for Lubricant Contamination
Avid Medical, Inc. is recalling 30 DAVINCI LAP/GYN kits (Model WRNM037-16) because they may be contaminated with a lubricant used during manufacturing.
Product
DAVINCI LAP/GYN; Model/Item Number (Kit): WRNM037-16;
Category
Medical Device
Distribution
Distributed nationwide