The Recall Desk

State

Alabama product recalls

73,806 recalls have nationwide distribution and so reach Alabama. 6,378 additional recalls listed Alabama specifically in their distribution scope.

What the numbers show

Total
6,378
Critical
1,129
Severe
1,605
Most recent
2026-11-04

Of the 6,378 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 1,605 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,378 recalls whose distribution notice names Alabama specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40601–40625 of 80184

  • ModerateFDA (Devices)·Z-2957-2018·2018-09-05

    Baxter Recalls FLOSEAL Special Applicator Tips Due to Plastic Formulation Error

    Baxter Healthcare is recalling FLOSEAL Special Applicator Tips because an incorrect plastic formulation was used in the blue luer component.

    Product
    FLOSEAL Special Applicator Tips in cartons labeled in part, "Floseal SPECIAL APPLICATOR TIPS***6 x Malleable Tip Trimmable Tip***Baxter***." The pouches inside the cartons are labeled in part, "Floseal SPECIAL APPLICATOR TIPS***Baxter***"."
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2948-2018·2018-09-05

    Medline Sodium Chloride Injection Recalled for Incorrect Overwrap Packaging

    Medline Industries is recalling 90,870 units of 0.9% Sodium Chloride Injection due to incorrect overwrap packaging. The product is intended for flushing IV catheters and tubing.

    Product
    Medline 0.9 % Sodium Chloride Injection, USP 5 mL in 10 mL Syringe ZR Intended for flushing IV catheters and IV tubing only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateNHTSA·18V591000·2018-09-05

    Mitsubishi Outlander Recall for Incorrect Rear Wheel Rim Size Label

    Mitsubishi is recalling 2018-2019 Outlander vehicles with 18-inch alloy wheels because the certification label lists an incorrect rear wheel rim size.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2953-2018·2018-09-05

    Sysmex Fluorocell PLT Reagent Recalled for Inaccurate Platelet Counts

    Sysmex America is recalling Fluorocell PLT reagent because it may cause falsely low platelet and immature platelet fraction results.

    Product
    Sysmex XN-Series Fluorocell PLT, Catalog #CD994563. Distributed in the U.S.A. by Sysmex America, Inc., Lincolnshire, IL. Fluorocell PLT is used to stain platelets in a diluted blood sample for the counting of platelets with the Sysmex XN-Series automated hematology…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2924-2018·2018-09-05

    Stryker Mako Vizadisc Knee Procedure Tracking Kit Recalled for Detection Issues

    Mako Surgical Corporation is recalling specific lots of the Stryker Mako Vizadisc Knee Procedure Tracking Kit because the reflective material may be damaged, preventing camera detection.

    Product
    Stryker Mako Vizadisc Knee Procedure Tracking Kit
    Category
    Medical Device
    Distribution
    35 states
  • ModerateFDA (Drugs)·D-1169-2018·2018-09-05

    Pfizer Recalls Children's Advil Suspension Due to Dosage Cup Labeling Error

    Pfizer is recalling 17,136 bottles of Children's Advil Suspension because the included dosage cup is marked in teaspoons while the label instructions use milliliters.

    Product
    CHILDRENS ADVIL — CHILDRENS ADVIL (IBUPROFEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1170-2018·2018-09-05

    Validus Recalls Calcitriol Oral Solution Due to Subpotency

    Validus Pharmaceuticals is recalling 7,864 bottles of Calcitriol Oral Solution because testing showed lower than expected potency at the 18-month stability time point.

    Product
    Calcitriol Oral Solution, 1 mcg/mL, 15 mL bottle, Rx Only, Distributed by: Ranbaxy Pharmaceuticals Inc. Jacksonville, FL 32257 USA, NDC 63304-241-59
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1907-2018·2018-09-05

    Equate High Performance Protein Shake Chocolate Recalled for Off Odor and Taste

    California Natural Products is recalling two lots of Equate High Performance Protein Shake Chocolate due to reports of off odor and off taste.

    Product
    equate High Performance Protein Shake: Chocolate, Naturally & Artificially Flavored, ready to drink; 11 FL OZ (325 mL), sold in 12 pack case: Case UPC: 6 81131 01580 6 Distributed by: Wal-Mart, Inc. Bentonville, AR
    Category
    Food
    Distribution
    18 states
  • LowFDA (Drugs)·D-1168-2018·2018-09-05

    Akorn Recalls Azelastine HCl Ophthalmic Solution Due to Impurities

    Akorn, Inc. is recalling specific lots of Azelastine HCl Ophthalmic Solution 0.05% because of out-of-specification results for Azelastine N-oxide.

    Product
    Azelastine HCl Ophthalmic Solution 0.05%, 6 mL in 10 mL HDPE bottle, 1 bottle per box, Rx only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-718-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1171-2018·2018-09-05

    Validus Recalls Rocaltrol Oral Solution Due to Lower Potency

    Validus Pharmaceuticals is recalling 696 bottles of Rocaltrol (calcitriol) Oral Solution because testing showed lower than expected potency.

    Product
    Rocaltrol (calcitriol) Oral Solution, 1 mcg/mL, 15 mL bottle, Rx only, Distributed by: Validus Pharmaceuticals, LLC Parsippany, NJ 07054 USA, NDC 30698-911-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1129-2018·2018-09-05

    Mayne Pharma Recalls Oxycodone and Acetaminophen Tablets Due to Labeling Error

    Mayne Pharma is recalling 6,456 bottles of Oxycodone and Acetaminophen Tablets due to a lot number labeling error on the primary container.

    Product
    Oxycodone and Acetaminophen Tablets, USP, 5 mg*/325 mg, 100-count bottle, Rx Only, Manufactured by: Mayne Pharma, Greenville, NC 27834, NDC 68308-841-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·18V584000·2018-09-04

    Collins School Bus Recall for Wheelchair Lift Cam Failure

    Collins Bus is recalling 2012-2018 school buses with Ricon wheelchair lifts because a cam may fail, causing the platform to rise too high and increasing injury risk.

    Product
    COLLINS — COLLINS SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V587000·2018-09-04

    Midwest Fire Recalls Emergency Vehicles Due to Brake Light Defect

    Midwest Fire is recalling 2017-2019 emergency vehicles because Whelen brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.

    Product
    MIDWEST FIRE — MIDWEST FIRE QUICK ATTACK, ALL-POLY SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V568000·2018-08-31

    Ford Recalls 2015-2018 F-150 Vehicles for Seat Belt Fire Risk

    Ford is recalling 2015-2018 F-150 Regular Cab and SuperCrew Cab vehicles because seat belt pretensioner sparks may ignite B-pillar materials, posing a fire risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V582000·2018-08-31

    FCCC Chassis Recall for Potential Rear Light Malfunction

    Daimler Trucks is recalling 2016-2019 FCCC chassis because a damaged module may cause rear lights to fail, increasing crash risk.

    Product
    FCCC — FCCC XCL, XBS, XCR, XCM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V583000·2018-08-31

    Eldorado Transit Bus Recall for Wheelchair Lift Cam Failure

    Eldorado is recalling 2012-2018 transit buses because a wheelchair lift cam may fail, allowing the platform to rise too high and increase injury risk.

    Product
    ELDORADO — ELDORADO, GOSHEN AERO ELITE, AEROTECH, IMPULSE, TRANSTECH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V578000·2018-08-30

    GM Recalls 2015-2016 Trucks and SUVs for Brake Pedal Nut Issue

    General Motors is recalling 2015-2016 Chevrolet and GMC vehicles because a brake pedal pivot nut may loosen, potentially rendering the brakes inoperative or interfering with the accelerator.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 1500, SIERRA 3500, SIERRA 2500, SILVERADO 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V581000·2018-08-30

    Daimler Trucks Recalls 2017-2019 Freightliner and Western Star Trucks for Fuel Line Defect

    Daimler Trucks is recalling 2017-2019 Freightliner and Western Star trucks because a restricted fuel pump cooling circuit screen may cause the fuel line to burst, leading to fuel leaks or engine stalling.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR 122SD, CASCADIA, CORONADO, 4900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V576000·2018-08-30

    GM Recalls 2018-2019 Vehicles for Rear Brake Caliper Coating Defect

    General Motors is recalling 2018-2019 Chevrolet, GMC, Buick, and Cadillac vehicles because rear brake caliper pistons may have insufficient coating, potentially reducing braking performance.

    Product
    CHEVROLET — CHEVROLET, CADILLAC, BUICK IMPALA, VOLT, XTS, BOLT EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V570000·2018-08-30

    Jayco Recalls 2018 Alante Vehicles Due to Hydraulic Hose Fire Risk

    Jayco is recalling 2018 Alante vehicles because damaged leveling system hydraulic hoses may leak fluid onto the exhaust system, increasing the risk of a fire.

    Product
    JAYCO — JAYCO ALANTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·18212·2018-08-30

    PetSmart Recalls Reptile Strip Lights Due to Fire Hazard

    PetSmart is recalling 20-inch and 30-inch reptile strip light fixtures because the bulbs can overheat and ignite the hood, posing a fire hazard.

    Product
    Reptile strip light fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide