State

Alabama product recalls

73,817 recalls have nationwide distribution and so reach Alabama. 6,378 additional recalls listed Alabama specifically in their distribution scope.

What the numbers show

Total: 6,378
Critical: 1,129
Severe: 1,605
Most recent: 2026-11-04

Of the 6,378 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 1,605 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,378 recalls whose distribution notice names Alabama specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45151–45175 of 80195

ModerateFDA (Devices)·Z-3053-2017·2017-08-30
Medtronic Curved Suction 90 Recalled for Verification Failure
Medtronic is recalling 75 Curved Suction 90 ENT instruments because they fail required pre-use verification checks.
Product
Medtronic Curved Suction 90 9733451 EM ENT, reusable, Rx. The firm name on the label is Medtronic Navigation, Inc., Louisville, CO. The suction devices are part of a family of reusable ENT instruments that are used with the StealthStationTM AxiEM surgical navigation system.…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1118-2017·2017-08-30
PD-Rx Recalls Phentermine Hydrochloride Capsules Due to Impurity Failures
PD-Rx Pharmaceuticals is recalling 3,440 bottles of Phentermine Hydrochloride capsules because stability tests showed out-of-specification unknown impurities.
Product
PHENTERMINE HYDROCHLORIDE — PHENTERMINE HYDROCHLORIDE (PHENTERMINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3067-2017·2017-08-30
Pentax Ultrasound Video Gastroscope Recalled for Incorrect Disinfection Instructions
Pentax of America Inc. is recalling 118 ultrasound video gastroscopes because the instructions for use contain an error in the disinfection step.
Product
Ultrasound Video Gastroscope, Model EG-3670URK, The product is intended to be used in combination with the ultrasound scanning unit made by Hitachi Medical Corporation, and the PENTAX Medical video processor to provide images for observation, diagnosis, imaging, or therapy…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1116-2017·2017-08-30
C. O. Truxton Recalls Phenobarbital Tablets Due to Labeling Error
C. O. Truxton is recalling specific lots of Phenobarbital Tablets USP, 15 mg, due to a label mixup that may result in mislabeled products.
Product
Phenobarbital Tablets USP, 15 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6160-10
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·17V533000·2017-08-29
Autocar Recalls 2015-2016 Xpeditor Vehicles for Steering Defect
Autocar is recalling 85 Xpeditor vehicles because a steering component may loosen, potentially causing a complete loss of steering and increasing crash risk.
Product
AUTOCAR — AUTOCAR XPEDITOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V525000·2017-08-29
Crane LET2 Trucks Recalled for Potential Steering Loss
Crane Carrier is recalling 2015-2016 LET2 vehicles because a loose tie rod could cause complete loss of steering.
Product
CRANE — CRANE LET2
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V534000·2017-08-29
Autocar Recalls 2016 Xpert and Xspotter Vehicles for Steering Defect
Autocar is recalling 2016 Xpert and Xspotter vehicles because a loose tie rod could cause a complete loss of steering and increase crash risk.
Product
AUTOCAR — AUTOCAR XPERT, XSPOTTER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V536000·2017-08-29
Volvo Recalls 2016 VNL and VNM Trucks for Steering Defect
Volvo is recalling 2016 VNL and VNM trucks because a loose tie rod may cause complete loss of steering, increasing crash risk.
Product
VOLVO — VOLVO VNM, VNL
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·17212·2017-08-29
Fabri-Tech Recalls Infant Rompers Due to Choking Hazard
Fabri-Tech is recalling about 6,500 infant shortall rompers sold at Cracker Barrel because shoulder buttons can detach, posing a choking hazard to children.
Product
Infant rompers
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·17V527000·2017-08-28
KME Recalls 2016 Predator Vehicles Due to Steering Defect
KME is recalling 2016 Predator Pumper, Rescue, and Airport Refueler vehicles because a loose tie rod could cause a complete loss of steering.
Product
KME — KME PREDATOR PUMPER, PREDATOR RESCUE, AIRPORT REFUELER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17E048000·2017-08-28
Ford Recalls Wheel Hub Bearings for 2011-2017 Explorer 4X2 Vehicles
Ford is recalling certain wheel hub bearing assemblies for 2011-2017 Ford Explorer 4X2 vehicles because they lack a self-retention feature, which could cause the wheel to separate.
Product
FORD — FORD EXPLORER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V531000·2017-08-28
Triton Recalls 2017 W-25 Trailers Due to Axle Bolt Tightening Defect
Triton Trailers is recalling 2017 W-25 Single Torsion Axle Trailers because improperly tightened axle mounting bolts may cause the axle to detach, increasing crash risk.
Product
TRITON — TRITON W-25
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V529000·2017-08-28
Ford Recalls 2017 F-150 and Mustang for Air Bag Inflator Defect
Ford is recalling 2017 F-150 and Mustang vehicles because the passenger air bag inflator may rupture in a crash, potentially causing serious injury or death.
Product
FORD — FORD F-150, MUSTANG
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V528000·2017-08-28
Ford Recalls 2017 Focus Vehicles for Rear Seat Back Weld Defect
Ford is recalling 2017 Focus vehicles because an insufficient weld on the rear left seat back may reduce its strength, increasing injury risk in a crash.
Product
FORD — FORD FOCUS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V530000·2017-08-28
Ford Recalls 2017 Models for Steering Gear Heat Shield Fastener Defect
Ford is recalling 2017 Explorer, Taurus, and Police Interceptor vehicles because steering gear heat shield fasteners may corrode and detach, potentially causing overheating and increased steering effort.
Product
FORD — FORD EXPLORER, TAURUS, POLICE INTERCEPTOR SEDAN, POLICE INTERCEPTOR UTILIT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V532000·2017-08-28
Hyundai Recalls 2017 Ioniq Electric Vehicles for Electronic Power Control Unit Defect
Hyundai is recalling 2017 Ioniq Electric vehicles because a manufacturing defect in the Electronic Power Control Unit may allow coolant to contact the circuit board, potentially causing a stall and increasing crash risk.
Product
HYUNDAI — HYUNDAI IONIQ ELECTRIC
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·17V526000·2017-08-28
Ford Recalls F-150 and F-250 Trucks for Seat Belt Defect
Ford is recalling 2015-2017 F-150 and 2017 F-250/F-350 trucks because the left rear inflatable seat belt buckle may detach, increasing injury risk.
Product
FORD — FORD F-150, F-250 SD, F-350 SD
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·17V524000·2017-08-25
Spartan Recalls 2016 Utilimaster Truck Bodies for Incorrect Tire Pressure Labels
Spartan Motors is recalling 2016 Utilimaster Truck Bodies because the printed tire pressure label is too low. This may cause under-inflation and tire blowouts.
Product
UTILIMASTER — UTILIMASTER TRUCK BODY
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·17V523000·2017-08-25
Forest River Recalls 2018 XLR ToyHaulers for Incorrect Tire Placard Information
Forest River is recalling 2018 XLR ToyHaulers because the Federal Placard may display incorrect tire and rim specifications, potentially leading to the installation of incorrect replacement tires.
Product
FOREST RIVER — FOREST RIVER XLR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V521000·2017-08-24
Western Star 4900 Trucks Recalled for Front Axle Spring Defect
Daimler Trucks North America is recalling 2017-2018 Western Star 4900 trucks because front axle weight capacity may exceed spring capacity, risking axle separation.
Product
WESTERN STAR — WESTERN STAR 4900
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·17V522000·2017-08-24
Thor Motor Coach Recalls 2018 RVs for Propane Hose Leak Risk
Thor Motor Coach is recalling 2018 Four Winds, Chateau, and Freedom Elite recreational vehicles because a liquid propane hose may sag and pinch, potentially causing a leak and fire risk.
Product
THOR MOTOR COACH — THOR MOTOR COACH FREEDOM ELITE, CHATEAU, FOUR WINDS
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·17210·2017-08-24
Arc'teryx Recalls Procline Ski Mountaineering Boots Due to Fall Hazard
Arc'teryx is recalling Procline ski mountaineering boots because a rear axis pin can dislodge, posing a fall hazard. No injuries have been reported.
Product
Arc'teryx Procline boots
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·17211·2017-08-24
Dr. Martens Vegan Boots Recalled for Benzidine Chemical Exposure Hazard
Airwair is recalling Dr. Martens Vegan 1460 boots in cherry red because the tongue lining contains benzidine. Consumers should stop using the boots and contact Dr. Martens for a refund or replacement.
Product
Dr. Martens Vegan boots
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1092-2017·2017-08-23
GEC LX Laxoplex Recalled for Undeclared Anabolic Steroids
Genetic Edge Compounds LLC is recalling GEC LX Laxoplex dietary supplements because FDA analysis found the product tainted with undeclared anabolic steroids and steroid-like substances.
Product
GEC LX Laxoplex 60 capsules Dietary Supplement, 60 count bottle, Manufactured by GEC, McKinney, TX, 75070, UPC: 700580499842
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1087-2017·2017-08-23
Biotech Underground Tri-Ton Hardcore Formula Recalled for Unapproved Ingredients
Dynamic Technical Formulations is recalling Biotech Underground Tri-Ton Hardcore Formula capsules because FDA testing found unapproved drug ingredients.
Product
Biotech Underground Tri-Ton Hardcore Formula capsules, 90-count bottle, Distributed by: Dynamic Technical Formulations 12850 Hwy 9 Suite 600-441 Alpharetta, GA 30004
Category
Drug
Distribution
Distributed nationwide