State

Alabama product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31101–31125 of 80099

ModerateFDA (Devices)·Z-2250-2020·2020-06-10
Nobel Biocare Recalls Dental Implant Healing Abutments Due to Sizing Error
Nobel Biocare is recalling specific dental implant healing abutments because they were packaged with the wrong size device.
Product
Healing Abutment Conical Connection RP 0 3.6 x 5mm, REF: 36644, UDI: 07332747034462 - Product Usage: Dental implant abutments are intended to be used in the upper or lower jaw and used for supporting tooth replacements to restore chewing function. The Healing Abutment is…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2184-2020·2020-06-10
Osteomed Recalls Osteovation Bone Void Filler Due to Shelf-Life Error
Osteomed is recalling 436 units of Osteovation 10cc Inject Formula because the labeled shelf-life may be incorrect, potentially affecting the product's setting characteristics.
Product
OSTEOVATION 10CC INJECT FORMULA. REF/UDI: 390-2010/00813845020061 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1284-2020·2020-06-10
Triova Recalls Estriol USP Micronized 5 G Due to Impurities
Triova Pharmaceuticals is recalling Estriol USP Micronized 5 G because the product failed specifications for organic impurities.
Product
Estriol USP Micronized 5 G, Rx only, Triova 115 W 3rd Street Suite 720 Tulsa, OK 74103, NDC 71092-9977-02
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1286-2020·2020-06-10
Teva Recalls Mixed Amphetamine Salts Tablets Due to Strength Variations
Teva Pharmaceuticals is recalling 41,348 bottles of 15 mg Mixed Amphetamine Salts tablets because some bottles may contain mixed strengths.
Product
DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2245-2020·2020-06-10
Philips Chest Pneumograph Recalled for Missing Natural Rubber Latex Labeling
Philips is recalling 1,075 Chest Pneumograph units because the labeling fails to state that the product contains natural rubber latex.
Product
Magnetic Resonance Imaging Diagnostic Device accessory - Product Usage: The chest pneumograph (also referred to as the pneumatic bellows, respiration bellows, or respiration sensor) monitors bellows-derived respiration by detecting abdominal or chest wall motion. The chest…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2181-2020·2020-06-10
Osteomed Recalls Osteovationex Bone Void Filler Due to Shelf-Life Error
Osteomed, LLC is recalling Osteovationex 3cc Inject Formula bone void fillers because the product may not maintain its setting characteristics for the labeled shelf-life duration.
Product
OSTEOVATIONEX 3CC INJECT FORMULA. REF/UDI: 390-0003/00813845020016 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2169-2020·2020-06-10
FDA Recalls Sterile Custom Surgical Packs from Unregistered Facility
American Contract Systems is recalling 2,868 sterile custom surgical packs because they were manufactured in a facility not registered by the FDA.
Product
Sterile Custom Packs to be used in surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2208-2020·2020-06-10
Bard Equistream XK Hemodialysis Catheter Recalled for Incorrect Sheath
Bard Peripheral Vascular Inc is recalling 215 Equistream XK Long-Term Hemodialysis Catheters because the kits contain an incorrect peel-apart introducer sheath.
Product
EQUISTREAM¿ XK Long-Term Hemodialysis Catheter. REF/UDI:5913230/:(01)00801741013843; 16F
Category
Medical Device
Distribution
24 states
ModerateFDA (Devices)·Z-2182-2020·2020-06-10
Osteomed Recalls Osteovationex Bone Void Filler Due to Shelf-Life Error
Osteomed, LLC is recalling 647 units of Osteovationex 5cc Inject Formula because the labeled shelf-life may be incorrect, potentially affecting the product's setting characteristics.
Product
OSTEOVATIONEX 5CC INJECT FORMULA. REF/UDI: 390-0005/00813845020023 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2185-2020·2020-06-10
Osteomed Recalls Osteovationex Bone Void Filler Due to Shelf-Life Error
Osteomed is recalling 300 units of Osteovationex 5cc ImpactFormula bone void filler kits because the labeled shelf-life may be incorrect, potentially affecting the product's setting characteristics.
Product
OSTEOVATIONEX 5CC IMPACTFORMULA. REF/UDI: 390-0205/00813845020047 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2178-2020·2020-06-10
FDA Recalls Sterile Custom Surgical Packs Due to Unregistered Facility
American Contract Systems is recalling 2,868 sterile custom surgical packs because they were manufactured in a facility not registered with the FDA.
Product
Sterile Custom Packs to be used in surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2249-2020·2020-06-10
Radiometer safeCLINITUBES Blood Samplers Recalled for Insufficient Aspiration
Radiometer Medical ApS is recalling safeCLINITUBES Blood Samplers because they may have insufficient aspiration capabilities, resulting in lost samples.
Product
safeCLINITUBES Blood Sampler;REF 942-969;D957P-70-45x1
Category
Medical Device
Distribution
38 states
ModerateFDA (Devices)·Z-2180-2020·2020-06-10
Osteomed Recalls Osteovationex Bone Void Filler Due to Shelf-Life Error
Osteomed, LLC is recalling 70 units of Osteovationex 2cc Inject Formula because the product may not maintain its setting characteristics for the labeled shelf-life duration.
Product
OSTEOVATIONEX 2CC INJECT FORMULA. REF/UDI: 390-0002/00813845020009 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2251-2020·2020-06-10
Abbott Accelerator APS Aliquoter Module Recalled for Sample Dilution Risk
Abbott is recalling 11 Accelerator APS Aliquoter Modules because a clot detection error may cause distilled water to dilute samples, leading to incorrect clinical results.
Product
Accelerator APS Aliquoter Module, List number: 07L40 - Product Usage: The ACCELERATOR APS Workcell is a modular system designed to automate sample handling and processing in the clinical laboratory. The system allows consolidations of multiple clinical chemistry and immunoassay…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·20V340000·2020-06-09
Mercedes-Benz Metris Recall for Driveshaft Attachment Defect
Daimler Vans USA is recalling 2019 Mercedes-Benz Metris vans because the driveshaft may not be attached correctly, risking loss of drive or unexpected airbag deployment.
Product
MERCEDES-BENZ — MERCEDES-BENZ METRIS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V337000·2020-06-09
Jayco Recalls 2020 Motorized RVs Due to Window Glass Detachment Risk
Jayco is recalling 2020 motorized recreational vehicles because the adhesive on frameless windows may fail, allowing glass to detach and become a projectile.
Product
JAYCO — JAYCO, ENTEGRA REDHAWK, QWEST, SENECA, EMBLEM
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V335000·2020-06-09
ARBOC Spirit of America and Liberty Buses Recalled for Fire Risk
ARBOC is recalling 113 Spirit of America and Spirit of Liberty buses because misrouted power cables may short circuit, increasing the risk of a fire.
Product
ARBOC — ARBOC SPIRIT OF AMERICA, SPIRIT OF LIBERTY
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V334000·2020-06-09
Chrysler Recalls 2017-2020 Pacifica Plug-in Hybrids for Fire Risk
Chrysler is recalling 2017-2020 Pacifica Plug-in Hybrids because a high-resistance electrical connection may overheat and cause a fire.
Product
CHRYSLER — CHRYSLER PACIFICA PLUG-IN HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V338000·2020-06-09
Highland Ridge RV Recalls 2020 Trailers Due to Window Glass Detachment Risk
Highland Ridge RV is recalling 80 units of 2020 Ridge, Open Range, and Silverstar trailers because window glass may detach and become a projectile.
Product
HIGHLAND RIDGE FW — HIGHLAND RIDGE FW, HIGHLAND RIDGE TT SILVERSTAR, MESA RIDGE, OPEN RANGE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V339000·2020-06-09
2020 Thor Motor Coach motorhome frameless windows may detach while driving
Thor Motor Coach is recalling certain 2020-2021 motorhomes because the adhesive bond in frameless windows may fail, allowing the glass to detach and become a projectile hazard while the vehicle is in motion.
Product
THOR MOTOR COACH — THOR MOTOR COACH AXIS, COMPASS, DELANO, GEMINI
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V336000·2020-06-09
Jayco Recalls 2020 Recreational Vehicles Due to Window Glass Detachment Risk
Jayco is recalling 2020 Eagle, Jay Flight, and other models because window glass may detach and become a projectile.
Product
JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL, JAYCO TRAVEL TRAILER EAGLE, JAY FLIGHT, EAGLE HT, NORTH POINT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V333000·2020-06-09
Lion Recalls 2012-2020 School Buses for Seat Belt Anchor Defect
Lion Electric Company is recalling 2012-2020 Lion 360 and Lion C school buses because the driver's seat belt anchor may be attached with incorrect hardware, potentially compromising safety in a crash.
Product
LION — LION LIONC, 360
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V331000·2020-06-08
Ford Recalls Vehicles Due to Door Latch Repair Defects
Ford is recalling specific 2011-2016 vehicles because previous door latch repairs may have been incomplete, potentially allowing doors to open while driving.
Product
FORD — FORD, LINCOLN C-MAX, FIESTA, FOCUS, FUSION
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V332000·2020-06-08
Ford Recalls 2014-2017 F-150 Trucks Due to Brake Master Cylinder Leak
Ford is recalling 2014-2017 F-150 trucks with 3.5L engines because the brake master cylinder may leak fluid, increasing the risk of a crash.
Product
FORD — FORD F-150
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V330000·2020-06-08
Forest River Recalls 2021 Prime Time Avenger Travel Trailers for Safety Chain Defect
Forest River is recalling 2021 Prime Time Avenger travel trailers because safety chains may be incorrectly attached, posing a risk of total trailer separation.
Product
FOREST RIVER — FOREST RIVER AVENGER
Category
Vehicle
Distribution
Distributed nationwide