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.

38576–38600 of 80118

SevereFDA (Devices)·Z-0742-2019·2019-01-30
Draeger Medical Recalls ID Circuit Watertrap Breathing Circuits Due to Assembly Error
Draeger Medical is recalling 25 units of ID Circuit Watertrap breathing circuits because they were incorrectly pre-assembled, creating a risk of incorrect connection or short circuit.
Product
ID Circuit Watertrap (P) 180, Catalog Number MP01341 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing…
Category
Medical Device
Distribution
12 states
SevereNHTSA·19V062000·2019-01-30
Proterra Recalls 2015-2018 Catalyst Buses Due to Tire Overload Risk
Proterra is recalling 2015-2018 Catalyst buses because a height control system may overload front tires, increasing crash risk.
Product
PROTERRA — PROTERRA CATALYST
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0744-2019·2019-01-30
Draeger ID Circuit Basic 180 Breathing Circuits Recalled for Assembly Defect
Draeger Medical is recalling 25 units of ID Circuit Basic 180 breathing circuits due to incorrect pre-assembly that may cause connection errors.
Product
ID Circuit Basic 180, Catalog Number MP01350 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets…
Category
Medical Device
Distribution
12 states
SevereFDA (Devices)·Z-0743-2019·2019-01-30
Draeger Medical Recalls ID Circuit Basic 250 Breathing Circuits
Draeger Medical is recalling 20 units of ID Circuit Basic 250 breathing circuits due to incorrect pre-assembly that may cause connection errors.
Product
ID Circuit Basic 250, Catalog Number MP01348 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets…
Category
Medical Device
Distribution
12 states
SevereFDA (Drugs)·D-0389-2019·2019-01-30
Dr. Reddy's Recalls Ezetimibe and Simvastatin Tablets Due to Foreign Substance
Dr. Reddy's is recalling specific bottles of Ezetimibe and Simvastatin tablets because black speckles were observed on the tablets.
Product
Ezetimibe and Simvastatin Tablets 10mg/80 mg, 1000-count bottles, Rx only, Manufactured by: Teva Pharmaceuticals Ind. Ltd. Jerusalem, 9777402, Israel; Distributed by: Dr. Reddy's Laboratories Inc. Princeton, NJ 08540 USA, NDC 43598-586-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0739-2019·2019-01-30
Draeger Medical Recalls VentStar Basic Breathing Circuits Due to Assembly Error
Draeger Medical is recalling 75 units of VentStar Basic (P) 250 breathing circuits because they were incorrectly pre-assembled, creating a risk of incorrect connection or short circuit.
Product
VentStar Basic (P) 250, Catalog Number MP00352 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia…
Category
Medical Device
Distribution
12 states
SevereFDA (Devices)·Z-0741-2019·2019-01-30
Draeger Medical Recalls 10 VentStar Anesthesia Breathing Circuits
Draeger Medical is recalling 10 units of VentStar Anesthesia WT(P) 180 breathing circuits due to incorrect pre-assembly that could cause incorrect connections.
Product
VentStar Anesthesia WT(P) 180, Catalog Number MP00374 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing…
Category
Medical Device
Distribution
12 states
SevereFDA (Drugs)·D-0384-2019·2019-01-30
Recall of Curaplex Epi Safe Kits Due to Incorrect Epinephrine Instructions
Bound Tree Medical is recalling Curaplex Epi Safe Kits because the instructions recommend an unapproved epinephrine dosage for young children.
Product
curaplex Epi Safe Kit, 8600-01101, contains:" 1ml Vial of Epinephrine " 1 Epi-Safe Syringe " 1 Safety Needle " 2 Alcohol Prep Pads " 1 Adhesive Dressing " 1 Insert, Rx Only. Distributed by Sarnova HC, LLC s family of companies: Bound Tree Medical, LLC, Cardio Partners, Inc.…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·19724·2019-01-30
Hot Mom Recalls Bed Rails for Federal Standard Violation and Entrapment Hazards
Hot Mom is recalling about 500 bed rails sold on Amazon.com because they fail to meet federal safety standards, posing entrapment and suffocation risks to young children.
Product
Bed Rails
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·19V074000·2019-01-30
BMW Recalls 2018-2019 X1 Models Due to Taillight Detachment Risk
BMW is recalling 2018-2019 X1 vehicles because contaminated hardware may cause taillights to crack and detach, creating a road hazard.
Product
BMW — BMW X1
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0771-2019·2019-01-30
Varian Eclipse Treatment Planning System Proton Algorithm Recall
Varian Medical Systems is recalling the Eclipse Treatment Planning System due to a software error in the Proton Convolution Superposition algorithm that miscalculates dose ranges for non-square CT images.
Product
Eclipse(TM) Treatment Planning System with Proton Convolution Superposition algorithm license only The Eclipse Treatment Planning System (Eclipse TPS) is used to plan radiotherapy treatments for patients with malignant or benign diseases. Eclipse TPS is used to plan external…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0761-2019·2019-01-30
Stihler PRISMAFLO II Blood Return Warmer Recalled for Burn Risk
Stihler Electronic Gmbh is recalling PRISMAFLO II blood return warmers because damage to the heating profile may cause low-level skin burns.
Product
Heating Profile PRISMAFLO II blood return warmer for Prismaflex Product Code: PF2-WP2618 Product Usage: The PRISMAFLO IIS warmer is used for warming return blood flow.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0772-2019·2019-01-30
Leica M220 F12 Surgical Microscope Recalled for Falling Optics Hazard
Leica Microsystems is recalling 15 Leica M220 F12 surgical microscopes because the optics may drop into the surgical field, risking contact with the patient.
Product
Leica M220 F12 surgical microscope The Leica M220 F12 surgical microscope is an optical instrument for improving the visibility of objects through magnification and illumination. It can be applied for observation and documentation and for human and veterinary medical…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0759-2019·2019-01-30
Stihler PRISMAFLO II S Blood Return Warmer Recalled for Burn Risk
Stihler Electronic Gmbh is recalling PRISMAFLO II S blood return warmers because damage to the heating profile may cause low-level skin burns.
Product
Heating Profile PRISMAFLO II S blood return warmer for Prismaflex Product Code: PF2-WP33 Product Usage: The PRISMAFLO IIS warmer is used for warming return blood flow.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0385-2019·2019-01-30
Bound Tree Medical Recalls Curaplex Epi Safe Training Kits Due to Labeling Errors
Bound Tree Medical is recalling 2,654 Curaplex Epi Safe training kits because the instructions recommend an unapproved epinephrine dosage for young children.
Product
Curaplex Epi Safe Kit, 8600-01102 TRAINING ONLY, Rx Only, Distributed by Sarnova HC, LLC s family of companies: Bound Tree Medical, LLC, Cardio Partners, Inc., Emergency Medical Products, Inc. & Tri-anim Health Services, Inc. 5000 Tuttle Crossing Blvd. Dublin, OH 43016
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0760-2019·2019-01-30
Stihler PRISMAFLO II S Blood Return Warmer Recalled for Burn Risk
Stihler Electronic Gmbh is recalling PRISMAFLO II S blood return warmers because damage to the heating profile may cause low-level skin burns.
Product
Heating Profile PRISMAFLO II S blood return warmer for Prismaflex Product Code: PF2-WP31 Product Usage: The PRISMAFLO IIS warmer is used for warming return blood flow.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0390-2019·2019-01-30
Lupin Recalls Fluocinolone Acetonide Topical Solution Due to Impurities
Lupin Pharmaceuticals is recalling 24,180 bottles of Fluocinolone Acetonide Topical Solution due to elevated impurities.
Product
FLUOCINOLONE ACETONIDE — FLUOCINOLONE ACETONIDE (FLUOCINOLONE ACETONIDE)
Category
Drug
Distribution
Distributed nationwide
SevereUSDA FSIS·009-2019·2019-01-29
Tyson Recalls Chicken Nuggets Due to Possible Rubber Contamination
Tyson Foods is recalling approximately 36,420 pounds of chicken nuggets that may contain rubber. Consumers should not eat the product and should discard it or return it to the store.
Product
Tyson Foods, Inc. — Tyson Foods, Inc. Recalls Chicken Nugget Products due to Possible Foreign Matter Contamination
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·19V061000·2019-01-29
Proterra Recalls 2015-2018 Catalyst Buses for Air Brake Moisture Risk
Proterra is recalling 2015-2018 Catalyst 40 transit buses because missing air brake components may allow moisture buildup, potentially leading to brake failure.
Product
PROTERRA — PROTERRA CATALYST
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V060000·2019-01-29
Honda Recalls Acura and Honda Vehicles for Fuel Pump Defect
Honda is recalling 2015-2019 Acura and Honda vehicles because fuel pump particulates may cause engine stalls, increasing crash risk.
Product
ACURA — ACURA, HONDA MDX, ACCORD, TLX
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19T001000·2019-01-29
Dynamic Tire Recalls Sailun Tires with Incomplete Identification Markings
Dynamic Tire Corp. is recalling specific Sailun tires because their sidewall markings lack the date of manufacture, failing federal safety standards.
Product
TIRES:MARKINGS recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V059000·2019-01-28
Gillig Recalls 2016-2018 Low Floor Buses for Steering Defect
Gillig is recalling 2016-2018 Low Floor buses because a steering draglink ball stud may not be properly tightened, increasing crash risk.
Product
GILLIG — GILLIG LOW FLOOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V058000·2019-01-28
Keystone Montana Recalled for Kitchen Slide Bolt Tire Contact Risk
Keystone RV is recalling 2019 Montana trailers because a kitchen slide adjustment bolt may contact the tire, potentially causing tire failure and increasing crash risk.
Product
KEYSTONE — KEYSTONE MONTANA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V055000·2019-01-28
Stoughton Recalls 2016-2019 DVW Trailers Due to Cracking Hitch Points
Stoughton is recalling 2016-2019 DVW trailers because the forward attachment points for the pintle mounting assembly may crack, potentially causing the trailer to detach from the tow vehicle.
Product
STOUGHTON — STOUGHTON DVW
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V057000·2019-01-28
Audi Recalls 2013-2016 A8 and S8 Models for Fuel Leak Risk
Volkswagen Group of America is recalling 2013-2016 Audi A8 and S8 vehicles because a fuel supply line may leak, increasing the risk of fire.
Product
AUDI — AUDI A8, S8
Category
Vehicle
Distribution
Distributed nationwide