The Recall Desk

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.

30801–30825 of 80099

  • LowFDA (Drugs)·D-1372-2020·2020-07-01

    Nabumetone Tablets Recalled for Missing Medication Guide Labeling

    American Health Packaging is recalling 265 cartons of Nabumetone Tablets because the carton label did not include the required statement to dispense with the accompanying Medication Guide.

    Product
    Nabumetone Tablets, USP, 500 mg, 100 Tablets per carton (10 tablets x 10 blister cards), Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217, NDC carton: 60687-374-01, NDC unit dose: 60687-374-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2407-2020·2020-07-01

    Utak Trace Elements Serum Control Recalled for Incorrect Reference Values

    Utak Laboratories is recalling 1,395 vials of NR Trace Elements Serum Control due to incorrect cadmium reference values and expected ranges.

    Product
    Utak NR Trace Elements Serum Control, 5 ml, REF 66816. The responsible firm on the label is UTAK LABORATORIES, INC., Valencia, CA. Control for in vitro diagnostics.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1342-2020·2020-07-01

    Pfizer Recalls Duavee Tablets Due to Failed Dissolution Specifications

    Pfizer is recalling Duavee tablets because they failed to meet dissolution specifications. The recall covers 544,400 packages distributed nationwide.

    Product
    Duavee (conjugated estrogens/bazedoxifene) tablets 0.45/20 mg, packaged in 2 blister cards containing 15 tablets each (30 tablets), Rx Only, Distributed by Wyeth Pharmaceuticals LLC A subsidiary of Pfizer In Philadelphia, PA 19101 Made in Ireland, NDC 00008-1123-12
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·20T012000·2020-06-30

    Bridgestone Recalls Mobile Crane Tires Due to Missing Safety Markings

    Bridgestone is recalling specific V-Steel tires for mobile cranes because they lack required DOT and safety markings, potentially leading to unsafe operating conditions.

    Product
    TIRES:MARKINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V379000·2020-06-30

    BMW Recalls 2020-2021 7 Series Models Due to Child Seat Anchor Issue

    BMW is recalling 2020-2021 7 Series vehicles because the rear middle child seat tether anchor may be inaccessible, increasing injury risk in crashes.

    Product
    BMW — BMW 750LI, M760I, B7 ALPINA, 740LI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·20V375000·2020-06-26

    Forest River Recalls 2021 Palomino Columbus Trailers Due to Furnace Vent Defect

    Forest River is recalling 2021 Palomino Columbus recreational trailers because improperly located furnace vents may allow exhaust fumes to enter the trailer, posing a risk of carbon monoxide poisoning.

    Product
    PALOMINO — PALOMINO COLUMBUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V376000·2020-06-26

    Forest River Rockwood Trailers Recalled for Incorrect Weight Rating Labels

    Forest River is recalling 2020-2021 Rockwood trailers with incorrect Gross Axle Weight Rating information on their Federal Placards. This could allow operators to unknowingly overload the vehicle, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER ROCKWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V377000·2020-06-26

    2021 Forest River Cherokee Wolf Pack Toyhauler Propane Routing Defect

    Forest River is recalling the 2021 Cherokee Wolf Pack toyhauler because the propane line may be routed around sharp edges, which can cause a leak and fire risk. Owners should contact Forest River at 1-260-499-2100 for a free repair.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE WOLF PACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V374000·2020-06-25

    Chrysler Recalls 2020 Ram 1500 and Promaster for Air Bag Defect

    Chrysler is recalling 2020 Ram 1500 pickups and Promaster vans because a side curtain airbag diffuser may detach, preventing proper inflation in a crash.

    Product
    RAM — RAM PROMASTER, 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E043000·2020-06-25

    Chrysler Recalls MOPAR Steering Drag Link Assemblies for Ram Trucks

    FCA US LLC is recalling specific MOPAR steering drag link assemblies for Heavy Duty Ram 2500 and 3500 trucks because a jam nut may loosen, risking loss of steering control.

    Product
    STEERING:LINKAGES:DRAG:LINK:CONNECTION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20753·2020-06-25

    Costway Recalls Baby Strollers Due to Fall and Strangulation Hazards

    Costway is recalling about 16,000 double baby strollers because they violate federal safety standards, posing fall, entrapment, and strangulation risks to children.

    Product
    Baby Strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1303-2020·2020-06-24

    Apotex Recalls Metformin Hydrochloride Extended-Release Tablets Due to NDMA Impurity

    Apotex Inc. is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above acceptable intake levels.

    Product
    Metformin Hydrochloride Extended-Release Tablets, USP 500 mg, 100 count bottles, Rx Only Manufactured by: Apotex, Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for: Apotex Corp. Weston, Florida 33326 NDC 60505-0260-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V370000·2020-06-24

    Triple E Recalls 2020 Wonder Motorhomes Due to Electrical Fire Risk

    Triple E is recalling 2020 Wonder W24MB, W24RTB, and W24FTB motorhomes because an improperly tightened electrical connection may short circuit and cause a fire.

    Product
    WONDER — WONDER W24RTB, W24MB, W24FTB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2235-2020·2020-06-24

    GE Healthcare Recalls Giraffe OmniBed Incubators Due to Oxygen Display Error

    GE Healthcare is recalling Giraffe OmniBed infant incubators equipped with Servo Oxygen modules because they may deliver a different oxygen level than displayed.

    Product
    Giraffe OmniBed with installed Servo Oxygen module. Infant incubator and warmer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1305-2020·2020-06-24

    AvKARE Recalls Metformin Hydrochloride Extended-Release Tablets Due to NDMA Impurity

    AvKARE Inc. is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.

    Product
    Metformin Hydrochloride Extended-Release Tablets, USP 500 mg, a) 50 count (NDC 50268-531-15); b) 90 count (NDC 42291-610-90); c) 180 count (NDC 42291-610-18); d) 360 count (NDC 42291-610-36); e) 1000 count (NDC 42291-610-10) bottles, Rx Only, Manufactured for: AvKARE, Inc.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2393-2020·2020-06-24

    Defibtech Recalls 860 Lifeline PRO AEDs Due to Shock Delivery Failure

    Defibtech is recalling 860 Lifeline PRO AEDs because a component issue may cause the device to abort or fail to deliver a shock.

    Product
    DDU-2400EN Lifeline PRO, UDI 00815098020270 - Product Usage: Automated External Defibrillators (AED) are indicated for use on victims of sudden cardiac arrest (SCA) who are: - unconscious and unresponsive, not breathing or not breathing normally.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V369000·2020-06-24

    Toyota Recalls Prius and Prius V for Hybrid System Shutdown Risk

    Toyota is recalling 2013-2015 Prius and 2014-2017 Prius V vehicles because excessive voltage in the inverter may cause the hybrid system to shut down, increasing crash risk.

    Product
    TOYOTA — TOYOTA PRIUS V, PRIUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E042000·2020-06-24

    Brake Parts Recalls Master Cylinders for Volkswagen Models Due to Piston Defect

    Brake Parts Inc. is recalling aftermarket brake master cylinders for specific Volkswagen models because the piston may pop out, risking a complete loss of braking.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:MASTER CYLINDER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2236-2020·2020-06-24

    GE Healthcare Recalls Giraffe Incubators with Servo Oxygen Module

    GE Healthcare is recalling Giraffe Incubators with Servo Oxygen modules because they may deliver different oxygen levels than displayed.

    Product
    Giraffe Incubator with installed Servo Oxygen module. Infant incubator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V373000·2020-06-24

    Toyota Recalls 2019-2020 RAV4 Models for Electric Power Steering Defect

    Toyota is recalling 2019-2020 RAV4 and 2020 RAV4 Hybrid vehicles because water may enter the steering gear box, causing a loss of electric power steering assist.

    Product
    TOYOTA — TOYOTA RAV4, RAV4 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2390-2020·2020-06-24

    Medtronic Bone Void Filler Recalled for Potential Setting Defects

    Medtronic is recalling 36 units of Bone Void Filler, Small, because the product may not maintain its setting characteristics for the labeled shelf-life, potentially increasing surgical time.

    Product
    Medtronic Bone Void Filler, Small - Product Usage: is an injectable, moldable and biocompatible calcium phosphate bone void filler. The single-use Medtronic Bone Void Filler Kit contains the necessary components for mixing of the bone void filler.
    Category
    Medical Device
    Distribution
    Distributed nationwide