State

Alabama product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39026–39050 of 80118

HighFDA (Drugs)·D-0266-2019·2018-11-28
L. Perrigo Recalls Calcium Carbonate Antacid Tablets Due to Metal Particles
L. Perrigo is recalling specific lots of calcium carbonate antacid tablets because they were found to contain metal particles.
Product
Antacid Tablets, Calcium Carbonate chewable tablets, 750mg, 60-count bottle, OTC, [Healthy Accents brand NDC: 55316-014-72, Distributed by DZA Brands, LLC, Salisbury, NC 28147, Scarborough, ME 04074], [HealthMart Pharmacy brand NDC: 62011-0295-1, Distributed by McKessen, One…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0481-2019·2018-11-28
GE Healthcare Recalls Giraffe Infant Warmers Due to Electric Leakage Risk
GE Healthcare is recalling 1,724 Giraffe infant radiant warmers worldwide due to a potential electric leakage hazard that could affect users.
Product
Giraffe Warmer. Device sold under the following product names: Giraffe Warmer and Giraffe Bedded Warmer. infant radiant warmer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0480-2019·2018-11-28
GE Healthcare Recalls Giraffe Incubator Carestations Due to Electric Leakage
GE Healthcare is recalling 1,724 Giraffe Incubator Carestations worldwide due to a potential electric leakage hazard that could affect users.
Product
Giraffe Incubator Carestation. Neonatal incubator. Device sold under the following product names: Carestation and Carestation CS1
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0486-2019·2018-11-28
Ascom Telligence Nurse Call System Recalled for Communication Failure
Ascom (US) Inc. is recalling 57 units of the Telligence Nurse Call System because a gateway defect may prevent device failures from being displayed at staff consoles.
Product
Ascom Telligence Nurse Call System
Category
Medical Device
Distribution
21 states
HighFDA (Devices)·Z-0479-2019·2018-11-28
GE Healthcare Recalls Giraffe OmniBed Neonatal Incubators Due to Electric Leakage
GE Healthcare is recalling 1,724 Giraffe OmniBed Carestation neonatal incubators worldwide due to a potential electric leakage hazard that could affect users.
Product
Giraffe OmniBed Carestation. Neonatal incubator. Device sold under the following product names: Carestation and Carestation CS1
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0484-2019·2018-11-28
GE Healthcare Panda Wall Mount Infant Radiant Warmer Recalled for Electric Leakage
GE Healthcare is recalling 1,724 Panda Wall Mount infant radiant warmers worldwide due to a potential electric leakage hazard that could affect users.
Product
Panda Wall Mount warmer. Infant radiant warmer
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0489-2019·2018-11-28
Merck Minicon Clinical Sample Concentrators Recalled for Performance Issues
Merck Millipore is recalling Minicon Clinical Sample Concentrators because they may take up to 24 hours to concentrate samples, delaying diagnostic tests.
Product
Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031 (Model: Minicon B-15) & 9051 (Model: Minicon CS-15) Minicon concentrators are non-sterile, disposable, multiwall ultrafiltration devices. Minicon¿ clinical sample concentrators are for in vitro diagnostic…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0476-2019·2018-11-28
Ortho-Clinical VITROS dLDL Reagent Recalled for Negatively Biased Results
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products dLDL Reagent GENs 26 and 27 because the in vitro diagnostic may produce negatively biased results.
Product
VITROS¿ Chemistry Products dLDL Reagent-GENs 26 & 27. In Vitro Diagnostic to quantitatively measure LDL Cholesterol (LDLC) Product Code: 6801728 UDI (10758750006793)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0283-2019·2018-11-28
Dr. Reddy's Recalls Clopidogrel Tablets Due to Dissolution Failure
Dr. Reddy's Laboratories is recalling specific lots of Clopidogrel Bisulfate tablets because they failed dissolution testing during stability checks.
Product
CLOPIDOGREL BISULFATE — CLOPIDOGREL BISULFATE (CLOPIDOGREL BISULFATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0275-2019·2018-11-28
Ecolab Recalls Medi-Stat Foam Hand Soap Due to Labeling Error
Ecolab Inc is recalling 14,108 bottles of Medi-Stat Foam Antimicrobial Hand Soap because the label may not match the formula in the bottle.
Product
Medi-Stat Foam, Antimicrobial Hand Soap, Chloroxylenol 0.5%, 1250 mL (42.3 fl oz), OTC, Ecolab, 370 Wabasha Street N, St. Paul, MN 55102, NDC 47593-503-59
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0388-2019·2018-11-28
GE Healthcare Recalls DeltaVision OMX SR Imaging Systems Due to Interlock Defect
GE Healthcare Biosciences is recalling 39 DeltaVision OMX SR Imaging Systems because the safety interlocks are not wired to be single-fault tolerant.
Product
DeltaVision OMX SR Imaging System Model Number: 29115476 The DeltaVision OMX SR Imaging System is a piece of laboratory equipment for super resolution imaging offluorescently-la beling biological samples. Techniques such as 3D Structured Illumination, Total Internal…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0273-2019·2018-11-28
Nitrofurantoin Capsules Recalled for Potential Cross-Contamination with Unrelated Ingredients
American Health Packaging is recalling specific lots of Nitrofurantoin Capsules due to potential cross-contamination with unrelated active ingredients.
Product
Nitrofurantoin Capsules USP (Monohydrate/Macrocrystals), 100 mg, 100-count Unit Dose Blisters, Rx only, Amerisource Health Services DBA American Health Packaging, 2550-A John Glenn Avenue Columbus, OH 43217, NDC 68084-446-01 (Individual Dose NDC: 68064-446-11)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0274-2019·2018-11-28
Ecolab Equi-Soft Foam Antimicrobial Hand Soap Recalled for Labeling Error
Ecolab is recalling Equi-Soft Foam Antimicrobial Hand Soap because the label may not match the formula in the bottle.
Product
ECOLAB — ECOLAB (BENZALKONIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·18V836000·2018-11-27
Audi Recalls A5 and A4 Allroad for Passenger Air Bag Defect
Volkswagen Group of America is recalling 2018 Audi A5 Sportback and 2017-2018 Audi A4 Allroad vehicles because a passenger air bag mounting screw may not be sufficiently tightened.
Product
AUDI — AUDI A5, A4 ALLROAD
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V839000·2018-11-27
Mercedes-Benz Recalls 2019 Models for Seat Belt Pre-Tensioner Defect
Mercedes-Benz is recalling 4,969 2019 vehicles because seat belt pre-tensioners may not activate in a crash, increasing injury risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH E 450, S 450, C 300, S 560 4MATIC
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V834000·2018-11-27
Ducati Recalls 2018-2019 Panigale V4 Motorcycles for Oil Cooler Defect
Ducati is recalling 2018-2019 Panigale V4 motorcycles because a cracked oil cooler port may cause an oil leak, increasing crash risk.
Product
DUCATI — DUCATI PANIGALE V4
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V840000·2018-11-27
Mercedes-Benz Recalls 2019 GLC 300 for Steering Assist Failure
Mercedes-Benz is recalling 2019 GLC 300 vehicles because a steering sensor may fail, deactivating power assist and increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ GLC 300
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18V833000·2018-11-27
Lamborghini Recalls Gallardo Vehicles Due to Software Warning Failure
Lamborghini is recalling 2011-2014 Gallardo vehicles because engine software may erase trouble codes, preventing warning lamps from illuminating for safety system failures.
Product
LAMBORGHINI — LAMBORGHINI GALLARDO
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·19039·2018-11-27
IKEA Recalls GLIVARP Dining Tables Due to Glass Laceration Hazard
IKEA is recalling GLIVARP extendable dining tables because the glass extension leaf can detach and fall, posing a laceration hazard.
Product
GLIVARP extendable dining tables
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·19719·2018-11-27
Lumber Liquidators Recalls 5-Gallon Buckets Due to Drowning Hazard
Lumber Liquidators is recalling 5-gallon mixing buckets because they lack required warning labels, posing a drowning risk to young children.
Product
5-Gallon mixing buckets
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·19040·2018-11-27
Öhlins Recalls Bicycle Forks Sold on Specialized Bicycles Due to Fall and Injury Hazards
Öhlins is recalling about 5,400 front air suspension bicycle forks sold on Specialized bikes because the air cartridge can spring out, posing fall and injury risks.
Product
Front air Suspension Bicycle Forks
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·18V835000·2018-11-27
Ducati Recalls 2017-2019 Motorcycles Due to Shift Knob Detachment Risk
Ducati is recalling 2,742 motorcycles because the shift knob may detach, preventing gear shifting and increasing crash risk.
Product
DUCATI — DUCATI SUPERSPORT, MONSTER 821, MONSTER 1200
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18E107000·2018-11-27
Wanda Recalls Aftermarket Windshields for 2014-2018 Toyota Highlanders
Fujian Wanda is recalling aftermarket replacement windshields for 2014-2018 Toyota Highlanders because water leaks into the wire harness, potentially damaging the Engine Control Module and causing the engine to stall.
Product
TOYOTA — TOYOTA HIGHLANDER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18V838000·2018-11-27
Mercedes-Benz Recalls 2018-2019 Models for Passenger Air Bag Display Error
Mercedes-Benz is recalling specific 2018-2019 C-Class and GLC-Class vehicles because the passenger air bag status may display incorrectly, potentially leaving occupants unaware the air bag is off.
Product
MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ C 300, AMG GLC63S, C 350 E, C 300 4MATIC
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V832000·2018-11-26
Airstream Recalls 2019 Interstate Motorhomes Due to Fuse Defect
Airstream is recalling 2019 Interstate motorhomes because incorrect fuses may allow battery cables to overheat, increasing fire risk.
Product
AIRSTREAM — AIRSTREAM INTERSTATE
Category
Vehicle
Distribution
Distributed nationwide