State

Alabama product recalls

73,509 recalls have nationwide distribution and so reach Alabama. 6,372 additional recalls listed Alabama specifically in their distribution scope.

What the numbers show

Total: 6,372
Critical: 1,131
Severe: 1,602
Most recent: 2026-10-14

Of the 6,372 recalls naming Alabama we have scored against our rubric, 1,131 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,602 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,372 recalls whose distribution notice names Alabama specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23726–23750 of 79881

SevereFDA (Drugs)·D-0463-2022·2022-02-09
Medroxyprogesterone Acetate Injection Recalled for Sterility Assurance
Ideal Specialty Apothecary is recalling Medroxyprogesterone Acetate Injection due to lack of assurance of sterility. The recall affects approximately 57,994 vials distributed nationwide.
Product
Medroxyprogesterone Acetate Injection, IM, 150 mg/mL, packaged in 1 ml Single Dose Vial, RX Only, Ideal Pharmacy, 2333 Morris Ave, Union, NJ 07083
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0530-2022·2022-02-09
Baxter SIGMA Spectrum infusion pumps recalled for medication delivery failures
Baxter is recalling 146,502 SIGMA Spectrum infusion pumps due to potential medication delivery failures that may occur without alerting clinicians. The issue is linked to administration set setup and occlusion alarm resolution.
Product
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8), Product code 35700BAX2.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0529-2022·2022-02-09
Baxter Spectrum IQ Infusion Pumps Recalled Due to Potential Medication Delivery Failure
Baxter Healthcare is recalling 241,304 Spectrum IQ infusion pumps due to potential medication delivery failure without user alert. The issue may occur during administration set setup or when occlusion alarms are not fully resolved.
Product
Baxter Spectrum IQ Infusion Pumps, Product code 3570009.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0480-2022·2022-02-09
COVID-19 Rapid Antigen Test Kit Distributed Without FDA Approval
CovClear COVID-19 Rapid Antigen Test kits (284,575 units) were distributed nationwide without FDA marketing approval, clearance, or authorization. All lots are recalled.
Product
CovClear COVID-19 Rapid Antigen Test, ATG 900-031
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0481-2022·2022-02-09
COVID-19 Test Kits Recalled for Unauthorized FDA Marketing and Sale
Empowered Diagnostics LLC recalled COVID-19 test kits (ImmunoPass, NAB 900-60) sold nationwide without FDA approval. Approximately 2,100 units were distributed without required marketing clearance or authorization.
Product
ImmunoPass , COVID-19 Neutralizing Antibody Test, NAB 900-60
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·22V071000·2022-02-09
Altec Recalls 2018-2021 Aerial Devices and Digger Derricks for Structural Defect
Altec is recalling 2018-2021 Aerial Devices and Digger Derricks because cracks in the subbase bulkhead plate can cause shear plate failure, increasing the risk of injury.
Product
ALTEC — ALTEC DIGGER DERRICK, AERIAL DEVICE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0552-2022·2022-02-09
Premier Rotaclone Medical Device Recalled Due to Improper Storage Conditions
Medline Industries is recalling 34 units of the Premier Rotaclone (Lot 696004N116) due to improper storage in temperature-controlled settings instead of required refrigeration. This may affect device performance or safety.
Product
Premier Rotaclone, Rx only
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22077·2022-02-09
Home Easy Geek Heat Personal Heaters Recalled for Fire Hazard
Home Easy is recalling about 3,000 Geek Heat DH-QN06 personal heaters because the toggle power switch can spark and cause a fire. The company has received three reports of fires caused by the switch, though no injuries or property damage have been reported.
Product
Personal Electric Heaters
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0540-2022·2022-02-09
DIXI Microdeep Depth Electrode sterile barrier packaging defect
DIXI Medical Microdeep Depth Electrodes are recalled due to potential deformation of the blister pack packaging that could compromise the sterile barrier. 345 units nationwide are affected.
Product
The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or Electrode) is a smooth electrode that is 0.8 mm in diameter with a rounded (hemispherical) tip. The electrode has multiple platinum/iridium contacts that are 2 mm long, with a total exploration length…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0534-2022·2022-02-09
Microdeep Depth Brain Electrodes recall due to sterile barrier compromise risk
DIXI Medical is recalling 484 Microdeep Depth Electrodes nationwide due to potential deformation of internal packaging that could compromise the sterile barrier of these brain recording devices.
Product
The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or Electrode) is a smooth electrode that is 0.8 mm in diameter with a rounded (hemispherical) tip. The electrode has multiple platinum/iridium contacts that are 2 mm long, with a total exploration length…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0545-2022·2022-02-09
Cryptococcal Antigen Test Kits Recalled for Reduced Detection Specificity
Immuno-Mycologics recalls 411 Cryptococcal Antigen test kits (lots F1021035, F1021036) for reduced specificity (90% vs. 99%), which may cause false-positive results leading to unnecessary anti-fungal therapy.
Product
CRYPTOCOCCAL ANTIGEN LATERAL FLOW ASSAY, IMMY, Lateral Flow Assay for the Detection of Cryptococcal Antigen in serum and CSF, REF CR2003, IVD, UDI: (01)00816387020919
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V073000·2022-02-09
Mercedes-Benz Recalls 2021 Sprinter Vans for Incorrect Weight Labeling
Daimler Vans USA is recalling 2021 Mercedes-Benz Sprinter vans because the gross vehicle weight rating may be incorrectly stated on the tire and loading label.
Product
MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 1500, SPRINTER 3500, SPRINTER 2500, SPRINTER 4500
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0535-2022·2022-02-09
DIXI Medical Microdeep Depth Electrode Sterile Barrier Compromise Recall
DIXI MEDICAL USA is recalling Microdeep Depth Electrodes used in neurological monitoring and stimulation due to potential deformation of the internal sterile packaging. The compromised sterile barrier could allow contamination before use.
Product
The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or Electrode) is a smooth electrode that is 0.8 mm in diameter with a rounded (hemispherical) tip. The electrode has multiple platinum/iridium contacts that are 2 mm long, with a total exploration length…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0553-2022·2022-02-09
ARIES HSV 1&2 Diagnostic Cassettes May Leak, Affecting Test Results
Luminex Corporation is recalling ARIES HSV 1&2 Assay cassettes (lot numbers AB3600A and AB3560A) due to a confirmed 0.9% leak rate. Leaking cassettes may cause incorrect or delayed test results.
Product
ARIES HSV 1&2 Assay, Catalog/REF# 50-10017
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0549-2022·2022-02-09
Philips eCareManager versions recalled due to unapproved Sentry Score software
Philips is recalling certain versions of eCareManager software because the Sentry Score feature was not approved by FDA prior to distribution. Users should contact Philips for updated information.
Product
eCareManager version 4.2.1, eCareManager version 4.3.2, eCareManager version 4.3.3, eCareManager version 4.5.1, eCareManager version 4.5.2, eCareManager version 4.6.0- a software tool intended for use by trained medical staff providing supplemental remote support to bedside…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22073·2022-02-09
Stack Em' Up Books Recalls Children's Stackable Toys for Excessive Lead Paint
Stack Em' Up Books is recalling Adam the Apple children's stackable toys because the surface paint contains lead levels that exceed the federal lead paint ban. Lead is toxic if ingested by young children and can cause adverse health effects.
Product
Adam the Apple™ Children's Stackable Toys
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0556-2022·2022-02-09
Pelvic floor repair device may lack required packaging component
FEMSelect Ltd is recalling 141 units of the EnPlace trans-vaginal pelvic floor repair system because certain lots may not have been packaged with the required Channel Tube Limiter accessory.
Product
The EnPlace is a single use trans-vaginal pelvic floor repair system which enables delivery of a tissue anchor to the ligaments of the vaginal cavity. The anchors are pre-loaded inside the device shaft and are ready for use. A thimble is also supplied, as an accessory for…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0537-2022·2022-02-09
DIXI Medical Microdeep Depth Electrode Packaging Defect Threatens Sterile Barrier
DIXI MEDICAL USA is recalling Microdeep Depth Electrodes due to potential packaging deformation that could compromise the sterile barrier. Approximately 2,720 units were distributed nationwide for use in brain recording and stimulation procedures.
Product
The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or Electrode) is a smooth electrode that is 0.8 mm in diameter with a rounded (hemispherical) tip. The electrode has multiple platinum/iridium contacts that are 2 mm long, with a total exploration length…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V070000·2022-02-09
2022 BMW X4 and Related Models Transmission Rollaway Risk Recall
BMW is recalling certain 2022 330i, 530i, X3, and X4 vehicles because the transmission mechatronics unit may not have been properly assembled, potentially causing an internal leak that could lead to vehicle rollaway and crash risk.
Product
BMW — BMW X4, X3, 330I, 530I
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0539-2022·2022-02-09
DIXI Medical Depth Electrodes recalled for potential sterile packaging defect
DIXI MEDICAL USA is recalling 461 Microdeep Depth Electrodes. The internal blister packaging may deform, potentially compromising the sterile barrier when removed from the protective Tyvek bag.
Product
The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or Electrode) is a smooth electrode that is 0.8 mm in diameter with a rounded (hemispherical) tip. The electrode has multiple platinum/iridium contacts that are 2 mm long, with a total exploration length…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V069000·2022-02-09
Seat belt pretensioners may explode in recalled 2021 Hyundai Accent vehicles
Hyundai recalls 2021 Accent vehicles due to defective seat belt pretensioners that may explode in a crash and project metal fragments, risking injury to occupants.
Product
HYUNDAI — HYUNDAI ACCENT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0542-2022·2022-02-09
DIXI Medical Microdeep Depth Electrode packaging defect may compromise sterility
DIXI MEDICAL USA is recalling Microdeep Depth Electrodes due to potential deformation of the internal packaging (blister pack) that could compromise the sterile barrier. The recall affects 365 units distributed nationwide.
Product
The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or Electrode) is a smooth electrode that is 0.8 mm in diameter with a rounded (hemispherical) tip. The electrode has multiple platinum/iridium contacts that are 2 mm long, with a total exploration length…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0536-2022·2022-02-09
DIXI Microdeep Depth Electrode packaging deformation poses sterility risk
DIXI Medical USA is recalling 2,141 Microdeep Depth Electrodes nationwide due to potential deformation of the blister pack that could compromise the sterile barrier when devices are removed from their Tyvek bags.
Product
The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or Electrode) is a smooth electrode that is 0.8 mm in diameter with a rounded (hemispherical) tip. The electrode has multiple platinum/iridium contacts that are 2 mm long, with a total exploration length…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V074000·2022-02-09
Maintainer Recalls 2021-2022 Truck-Mounted Cranes Due to Fire Risk
Maintainer is recalling 2021-2022 truck-mounted cranes because an incorrectly installed guard may damage fuel hoses or cables, increasing fire risk.
Product
MAINTAINER — MAINTAINER CRANE W/ SERVICE BODY
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·22072·2022-02-09
Petzl Scorpio Eashook Lanyards with Carabiners Recalled for Fall Risk
Petzl is recalling about 230 Scorpio Eashook Lanyards with Carabiners because the carabiner's automatic gate-closing system can malfunction, creating a risk of serious injury or death.
Product
Scorpio Eashook Lanyards with Carabiners
Category
Consumer Product
Distribution
Distributed nationwide