State

Alabama product recalls

73,737 recalls have nationwide distribution and so reach Alabama. 6,377 additional recalls listed Alabama specifically in their distribution scope.

What the numbers show

Total: 6,377
Critical: 1,129
Severe: 1,604
Most recent: 2026-10-28

Of the 6,377 recalls naming Alabama we have scored against our rubric, 1,129 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,604 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,377 recalls whose distribution notice names Alabama specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32251–32275 of 80114

ModerateFDA (Devices)·Z-1349-2020·2020-03-04
Randox RX Daytona Plus Clinical Chemistry Analyzer Software Recall
Randox Laboratories is recalling RX Daytona Plus clinical chemistry analyzers to fix software issues causing incorrect sample ordering and quality control flags.
Product
RX Daytona Plus (with ISE/without ISE); Models Nos. RX4040 (w/ISE) and RX4041 (without ISE) - Product Usage: A fully automated, random access, clinical chemistry analyzer complete with dedicated analyzer software. For use in clinical laboratories.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1363-2020·2020-03-04
Siemens ADVIA Chemistry Lipase Recalled for Calibration Failures
Siemens Healthcare Diagnostics is recalling ADVIA Chemistry Lipase reagents due to customer complaints about failed calibrations and increased imprecision in quality control and patient samples.
Product
ADVIA Chemistry Lipase, Ref. No. 01984894 B01-4840-01, Siemens Material No. 10311896, UDI 00630414482446 - Product Usage: Lipase measurements are used in the diagnosis and treatment of diseases of the pancreas, such as acute pancreatitis and obstruction of the pancreatic duct.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1382-2020·2020-03-04
Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Data Errors
Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour data.
Product
CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 5.6MM(P) X 3MM(H) Reference Number: IEHA553
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0745-2020·2020-03-04
Domino Brown Sugar Recalled for Possible Foreign Material
Domino Foods Inc is recalling 50 LB bags of Premium Pure Cane Golden Light Brown Sugar due to possible foreign material.
Product
Domino Premium Pure Cane Golden Light Brown Sugar, 50 LB bag, UPC 049200009727, Lots 50041 (Best By Jan 20, 2022), 50042 (Best By Jan 21, 2022), 50043 (Best By Jan 22, 2022)
Category
Food
Distribution
23 states
ModerateFDA (Food)·F-0743-2020·2020-03-04
Domino Foods Recalls C&H Golden Brown Sugar Due to Foreign Material
Domino Foods Inc is recalling specific lots of C&H Pure Cane Sugar Golden Brown due to possible foreign material contamination.
Product
C&H Pure Cane Sugar Golden Brown, 32 oz (2 LB) plastic bag, UPC 015800090038, Lots 50042 (Best By Jan 21, 2022) & 50043 (Best By Jan 22, 2022)
Category
Food
Distribution
23 states
ModerateFDA (Devices)·Z-1345-2020·2020-03-04
Philips DigiTrak XT Holter Recorder Software Recall for Malfunction
Philips is recalling DigiTrak XT Holter Recorders because a software defect causes the device to fail when an AAA battery is present.
Product
Philips DigiTrak XT Holter Recorder Software version number B.1 and C.2. The DigiTrak XT Recorder is available in four different configurations. Service tag numbers for these configurations are as follows: - 453564067151 24-Hour Configuration - 453564067161 48-Hour…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0749-2020·2020-03-04
Domino Foods Recalls SYSCO Light Brown Cane Sugar for Foreign Material
Domino Foods Inc is recalling specific lots of SYSCO Classic Light Brown Cane Sugar due to possible foreign material. The product was distributed to 23 states and Saudi Arabia.
Product
SYSCO Classic Light Brown Cane Sugar, 32 oz (2 LB) plastic bag, UPC 074865755368, Lots 50042 (Best By Jan 21, 2022) & 50051 (Best By Jan 27, 2022)
Category
Food
Distribution
23 states
ModerateFDA (Devices)·Z-1366-2020·2020-03-04
Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error
Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they may cause incorrect rotation and margin misalignment in dental impressions.
Product
CERTAIN BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 3.8MM(P) X 3MM(H) Reference Number: IEHA343
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0859-2020·2020-03-04
Akorn Recalls Sodium Chloride Ophthalmic Ointment Due to Particulate Matter
Akorn, Inc. is recalling specific lots of Sodium Chloride Ophthalmic Ointment USP, 5%, due to the presence of brown particulate matter inside the tubes.
Product
Sodium Chloride Ophthalmic Ointment USP, 5%, 3.5 g tubes, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC 17478-622-35
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1389-2020·2020-03-04
LivaNova SMART PERFUSION PACK INSPIRE 8S Recalled for Incorrect Cuvette Packaging
LivaNova USA Inc. is recalling 27 SMART PERFUSION PACK INSPIRE 8S units because they were packaged with the incorrect cuvette component.
Product
LivaNova SMART PERFUSION PACK INSPIRE 8S - Product Usage: The affected product is a perfusion tubing pack use in surgical procedures requiring extracorporeal support. The perfusion tubing packs include the cuvette used with equipment to monitor blood.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1063-2020·2020-03-04
Breckenridge Recalls Zoledronic Acid Injection Due to Impurity Failures
Breckenridge Pharmaceutical is recalling 900 vials of Zoledronic Acid Injection because stability testing revealed out-of-specification impurities.
Product
Zoledronic Acid Injection 5 mg/100 mL (0.05 mg/mL), Solution for Intravenous Infusion, Sterile Solution, 100 mL Single - Dose Vial per Carton, Rx Only, Distributed by: Breckenridge Pharmaceutical, Inc., Boca Raton, FL 33487, Manufactured by: Pharmaceutics International, Inc.…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0856-2020·2020-03-04
Golden State Medical Supply Recalls Tramadol Tablets Due to Labeling Error
Golden State Medical Supply is recalling Tramadol Hydrochloride 50 mg tablets because the patient leaflets contain incorrect dosing instructions for unscored tablets.
Product
TRAMADOL HYDROCHLORIDE Tablets, USP, 50 mg, Rx Only a)100-count bottles (NDC 60429-588-01) b) 500-count bottle (NDC 60429-588-05) Manufactured by Teva Czech Industries, s.r.o. Opava-Komarov, Czech Republic, Packaged by GSMS Incorporated, Camarillo, CA 93012
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0860-2020·2020-03-04
Akorn Recalls Well at Walgreens Sodium Chloride Ophthalmic Ointment Due to Particulate Matter
Akorn, Inc. is recalling specific tubes of Well at Walgreens Sodium Chloride Ophthalmic Ointment USP, 5%, due to the presence of brown spots identified as tin with trace copper.
Product
Well at Walgreens Sodium Chloride Ophthalmic Ointment USP, 5%, 3.5 g tubes, Distributed by: Walgreen Co. 200 Wilmot Rd., Deerfield, IL 60015. NDC 0363-9050-00.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0861-2020·2020-03-04
CVS Health Sodium Chloride Ophthalmic Ointment Recalled for Particulate Matter
Akorn, Inc. is recalling CVS Health Sodium Chloride Ophthalmic Ointment USP, 5%, due to the presence of brown spots identified as tin with trace copper inside the tubes.
Product
CVS Health Sodium Chloride Ophthalmic Ointment USP, 5%, 3.5 g tubes, Distributed By: CVS Pharmacy Inc. One CVS Drive, Woonsocket, RI 02895, NDC 59779-303-01
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·20V126000·2020-03-03
Thomas Built Buses Recall 2019-2020 Models for Brake Caliper Bolt Issue
Daimler Trucks is recalling 581 Thomas Built school buses because loose brake caliper bolts may reduce braking effectiveness, increasing crash risk.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2, SAF-T-LINER HDX, SAF-T-LINER EFX
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V125000·2020-03-03
Blue Bird Recalls School Buses Due to Seat Barrier Defect
Blue Bird is recalling 2008-2021 Vision and All American school buses because the seat barrier behind the driver may be missing a reinforcing bracket, increasing injury risk in a crash.
Product
BLUE BIRD — BLUE BIRD ALL AMERICAN, VISION SCHOOL BUS, VISION TRANSIT BUS, VISION
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V127000·2020-03-03
Daimler Trucks Recalls 2019-2020 Vehicles for Brake Caliper Bolt Issue
Daimler Trucks North America is recalling 2,585 2019-2020 trucks because brake caliper mounting bolts may be loose, increasing crash risk.
Product
WESTERN STAR — WESTERN STAR, FREIGHTLINER, FCCC 4700, 5700, BUSINESS CLASS M2, XBR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V124000·2020-03-03
Jeep Recalls Wrangler and Gladiator Vehicles for Clutch Fire Risk
Chrysler is recalling 2018-2020 Jeep Wrangler and 2020 Gladiator vehicles with manual transmissions because the clutch pressure plate may overheat and fracture, increasing the risk of fire or crash.
Product
JEEP — JEEP WRANGLER, GLADIATOR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20T005000·2020-03-03
Tires Recalled for Sidewall Separation Defect
Sentury Tire is recalling certain sidewall-tired models because a manufacturing defect causes the sidewall to separate, potentially leading to tire failure and increased crash risk.
Product
TIRES:SIDEWALL recall
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·20V123000·2020-03-02
Lion Recalls 2015-2020 School Buses Due to Steering Bolt Defect
Lion Electric Company is recalling 2015-2020 Lion C and 360 school buses because steering bolts may loosen, causing a loss of control.
Product
LION — LION 360, LIONC
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20E010000·2020-03-02
Ford and Volvo Recall Vehicles with Defective Kiekert Door Latches
Ford and Volvo are recalling vehicles with specific Kiekert door latches that may break in high heat, leaving doors unlatched.
Product
LATCHES/LOCKS/LINKAGES:DOORS:LATCH recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V121000·2020-02-28
Hyundai Recalls 2013-2014 Sonata Vehicles for Fuel Hose Fire Risk
Hyundai is recalling 2013-2014 Sonata vehicles because a fuel hose may crack, causing a leak and increasing fire risk. Dealers will inspect and repair the hose free of charge.
Product
HYUNDAI — HYUNDAI SONATA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V120000·2020-02-28
Pierce Emergency Fire Vehicles Recalled for Aerial Device Cracks
Pierce is recalling 2019-2020 Arrow XT, Enforcer, Impel, and Velocity fire vehicles because cracks in the aerial device tube may cause it to fall.
Product
PIERCE — PIERCE ARROW XT, IMPEL, VELOCITY, ENFORCER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V122000·2020-02-28
Hyundai Recalls 2020 Sonata Vehicles for Incorrect Tire Size Labeling
Hyundai is recalling 2020 Sonata vehicles because the tire pressure label and owner's manual list an incorrect tire size. This error may lead owners to install the wrong tires, affecting vehicle handling.
Product
HYUNDAI — HYUNDAI SONATA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V119000·2020-02-28
Forest River Shasta Trailers Recalled for Tire Clearance Issues
Forest River is recalling 2020 Shasta SST240TH and SST260TH trailers because tires may contact the wheel well, risking tire failure and loss of control.
Product
FOREST RIVER — FOREST RIVER SHASTA
Category
Vehicle
Distribution
Distributed nationwide