The Recall Desk

State

Alabama product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

34926–34950 of 80115

  • HighFDA (Devices)·Z-2440-2019·2019-09-11

    Siemens SOMATOM CT Software Recall for Workflow Interruptions

    Siemens Medical Solutions is recalling syngo.CT software version VA48A_SP5.5 for specific SOMATOM CT models due to scanning workflow interruptions and unexpected user notifications.

    Product
    syngo.CT software version VA48A_SP5.5 in the following SOMATOM computed tomography models: SOMATOM Definition Edge-Model #10590000; SOMATOM Definition AS Model #8098027; SOMATOM Definition Flash Model #10430603
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2473-2019·2019-09-11

    B. Braun Medical Recalls Accu-Bloc Perifix Kits Due to Filter Damage

    B. Braun Medical is recalling 200 units of Accu-Bloc Perifix Kits because damaged filter membranes may prevent the device from achieving required filter capacity.

    Product
    CE18HKN ACCU-BLOC PERIFIX KIT NRFIT Catalog # 339189
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-2435-2019·2019-09-11

    Integra Jarit GEMINI CLAMP Recalled Due to Potential Instrument Breakage

    Integra LifeSciences Corp. is recalling 237 units of the Jarit GEMINI CLAMP because a small crack may cause corrosion and breakage after repeated sterilization.

    Product
    Integra Jarit GEMINI CLAMP 9 1/4 inch - used in vascular and cardiothoracic procedures used for clamping and occluding vessels. Cat. #140-332
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2355-2019·2019-09-11

    Norm-O-Temp 111Z Medical Device Recalled for Missing Tissue Damage Warning

    Cincinnati Sub-Zero Products LLC is recalling Norm-O-Temp model 111Z devices because the manual lacks instructions warning that exceeding 40 Celsius for extended periods can cause tissue damage.

    Product
    Norm-O-Temp model 111Z
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-2469-2019·2019-09-11

    B. Braun Medical Recalls Epidural Tuohy Needle Filters Due to Membrane Damage

    B. Braun Medical is recalling 540 units of CE17TKN epidural Tuohy needle filters because the filter membrane is damaged, preventing the device from achieving its intended filter capacity.

    Product
    CE17TKN CONT EPIDURALTUOHY NRFIT Catalog # 339183
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-2471-2019·2019-09-11

    B. Braun Medical Recalls Con Epi Tray Due to Filter Membrane Damage

    B. Braun Medical is recalling 200 units of Con Epi Trays because damage to the filter membrane prevents the device from achieving its required filter capacity.

    Product
    CE17TKFCSN CON EPI TRAY W/17G TUHY NRFIT Catalog # 339187
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-2472-2019·2019-09-11

    B. Braun Medical Recalls Accu-Bloc Perifix Kits Due to Filter Damage

    B. Braun Medical is recalling 3,820 units of Accu-Bloc Perifix Kits because damage to the filter membrane prevents the device from achieving its intended filter capacity.

    Product
    CE18TKN ACCU-BLOC PERIFIX KIT NRFIT Catalog # 339188
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-2467-2019·2019-09-11

    B. Braun Recalls Spinal and Epidural Trays Due to Filter Damage

    B. Braun Medical is recalling 200 units of spinal and epidural trays because the filter membrane is damaged, preventing the device from achieving required filter capacity.

    Product
    ES1827KN SPINAL/EPIDURAL TRAY NRFIT Catalog # 339115
    Category
    Medical Device
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-2437-2019·2019-09-11

    Heidelberg SPECTRALIS Ophthalmic Imaging Device Recalled for Data Display Error

    Heidelberg Engineering is recalling 29 SPECTRALIS ophthalmic imaging devices because a software configuration error may cause incorrect display of patient master data.

    Product
    SPECTRALIS with HEYEX2 image management system. a non-contact ophthalmic diagnostic imaging device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2441-2019·2019-09-11

    Fujifilm FDR Go Plus X-ray System Recalled for Software Glitch

    Fujifilm is recalling 174 FDR Go Plus mobile X-ray systems because a graphics driver issue may cause the device to display a Blue Screen of Death.

    Product
    Fujifilm FDR Go Plus mobile X-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2445-2019·2019-09-11

    Roche Tina-Quant Myoglobin Gen. 2 Assay Recalled for QC Imprecision

    Roche is recalling Tina-Quant Myoglobin Gen. 2 assays due to signal drops causing calibration failures and QC imprecision on specific analyzers.

    Product
    The Tina-Quant Myoglobin Gen. 2 Tests system is an immuno-turbidimetric assay for the quantitative in vitro determination of myoglobin in human serum and plasma on Roche automated clinical chemistry analyzers
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2475-2019·2019-09-11

    Alere Cholestech LDX Analyzer Recalled for Reversed Power Supply Polarity

    Alere San Diego, Inc. is recalling 186 Alere Cholestech LDX Analyzer kits because the power supplies have reversed polarity, rendering the devices inoperable.

    Product
    Alere Cholestech LDX Analyzer, model # 14-874 containing power supplies with the identifying codes of 1837d and 1843d - Product Usage: The Alere Cholestech LDX System is a small, portable analyzer and test cassette system. The System is for in vitro diagnostic use only. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2433-2019·2019-09-11

    Getinge CO2 Absorber Recalled for Reversed Expiration and Manufacturing Dates

    Getinge is recalling 1,444 boxes of disposable CO2 absorbers because the expiration and manufacturing dates on the labels are reversed.

    Product
    Getinge MCC Flow i Disposable CO2 absorber, used in anesthesia systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·19204·2019-09-10

    Ragdoll & Rockets Recalls Children's Loungewear for Flammability Violation

    Ragdoll & Rockets is recalling about 14,100 units of children's loungewear because the items fail to meet federal flammability standards for sleepwear, posing a risk of burn injuries.

    Product
    Children's loungewear
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19200·2019-09-10

    Healing Solutions Recalls Essential Oils for Child-Resistant Packaging Failure

    Healing Solutions is recalling Wintergreen and Birch essential oils because the bottles lack required child-resistant caps, posing a poisoning risk to young children.

    Product
    Healing Solutions Wintergreen and Birch 100 percent Pure Therapeutic Grade Essential Oils
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19203·2019-09-10

    DIANA Stormrider Gen 2 Air Rifles Recalled for Unexpected Discharge Risk

    DIANA is recalling Stormrider Gen 2 air rifles because they can unexpectedly discharge even when the safety is engaged, posing a risk of serious injury or death.

    Product
    DIANA® Stormrider Gen 2 Air Rifles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V647000·2019-09-09

    Isuzu Recalls 2017-2019 Trucks for Potential Electrical Wiring Defect

    Isuzu is recalling 2017-2019 N-Series and Chevrolet Low Cab Forward trucks because a loose bolt in the relay box may cause electrical failure and vehicle stalling.

    Product
    CHEVROLET — CHEVROLET, ISUZU LOW CAB FORWARD 6500, LOW CAB FORWARD 4500, LOW CAB FORWARD 3500, N-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V648000·2019-09-09

    Mercedes-Benz Recalls 2020 GLE Models for Missing Head Restraint Manual Info

    Mercedes-Benz is recalling 2020 GLE 350 and GLE 450 vehicles because the owner's manuals lack instructions for adjusting third-row head restraints, violating federal safety standards.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350, GLE 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E060000·2019-09-06

    TAP Recalls Pro Comp Lug Nuts Due to Incorrect Sizing

    TAP Worldwide is recalling 840 Pro Comp Extended Thread lug nuts that may be incorrectly sized. The defect could prevent proper tightening, leading to lug stud failure and increased crash risk.

    Product
    WHEELS:LUGS/NUTS/BOLTS/STUDS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V643000·2019-09-06

    GM Recalls 2020 Buick Enclave and Chevrolet Traverse for Frame Rail Crack

    General Motors is recalling 2020 Buick Enclave and Chevrolet Traverse vehicles because a crack in the right-hand frame rail may reduce crash performance and increase injury risk.

    Product
    BUICK — BUICK, CHEVROLET ENCLAVE, TRAVERSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V645000·2019-09-06

    GM Recalls Trucks and SUVs for Brake Vacuum Pump Defect

    General Motors is recalling 2014-2018 Chevrolet, GMC, and Cadillac vehicles because a vacuum pump defect may reduce brake assist, increasing stopping distance.

    Product
    CHEVROLET — CHEVROLET, GMC, CADILLAC SUBURBAN, SILVERADO 1500, SIERRA 1500, YUKON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V644000·2019-09-06

    GM Recalls 2019 Chevrolet Express and GMC Savana for Seatbelt Warning Defect

    General Motors is recalling 2019 Chevrolet Express and GMC Savana vehicles because the seatbelt-unfastened warning light may fail to illuminate for five seconds after ignition.

    Product
    GMC — GMC, CHEVROLET SAVANA, EXPRESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V646000·2019-09-06

    Temsa Recalls Buses Due to Inadequate Emergency Exit Window Labels

    Temsa is recalling 2013-2020 TS35C, TS35E, and TS45 buses because emergency exit window labels may not clearly describe how to open them quickly.

    Product
    TEMSA — TEMSA TS35C, TS45, TS35E
    Category
    Vehicle
    Distribution
    Distributed nationwide