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.

34151–34175 of 80115

  • ModerateFDA (Devices)·Z-0337-2020·2019-11-13

    Zimmer Biomet Recalls Cephalomedullary Nails Due to Packaging Adhesion

    Zimmer Biomet is recalling 5.4 million cephalomedullary nails because non-highly polished implants may adhere to the packaging bags.

    Product
    Cephalomedullary Nail (CMN), Various sizes, Item Nos. 47249318009 47249318010 47249318011 47249318013 47249318014 47249318109 47249318110 47249318111 47249318113 47249318114 47249318209 47249318210 47249318211 47249318213 47249318214 47249318309 47249318310…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0316-2020·2019-11-13

    Zimmer Biomet Recalls Prox Lat Humeral Lock Plates Due to Packaging Adhesion

    Zimmer Biomet is recalling Prox Lat Humeral Lock Plates because non-highly polished implants may adhere to the LDPE bag packaging.

    Product
    PROX LAT HUMERAL LOCK PLATE, Item Nos. 47235800104 47235800106 47235800108 47235800112 47235800116 47235800204 47235800206 47235800208 47235800212
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0330-2020·2019-11-13

    Zimmer Biomet Recalls Connection Screws for NCB Plates

    Zimmer Biomet is recalling 5,459,583 Connection Screws for NCB Plates because non-highly polished implants may adhere to the LDPE bag.

    Product
    Connection Screw for NCB Plate, Item No. 0202266002
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0306-2020·2019-11-13

    Zimmer Biomet Recalls Ankle Implants Due to Packaging Adhesion

    Zimmer Biomet is recalling 5.4 million ankle implants because non-highly polished devices may adhere to the packaging bag.

    Product
    TM Ankle and Ankle Talus L/R, Item Nos. 00450001100 00450001200 00450001300 00450001400 00450001500 00450001600 00450002100 00450002200 00450002300 00450002400 00450002500 00450002600
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0311-2020·2019-11-13

    Zimmer Biomet Recalls Spinal Plates Due to Packaging Adhesion

    Zimmer Biomet is recalling specific spinal plates because non-highly polished implants may adhere to the packaging bag.

    Product
    SM DIS VOL/DORS RAD LAT COL PLATE, Item Nos. 47235801404 47235802102 47235802103 47235802104 47235802106 47235802108 47235802203 47235802204 47235802206 47235802208 47235802210
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0283-2020·2019-11-13

    Randox Liquid Protein Calibrators Recalled for Rheumatoid Factor Value Adjustment

    Randox Laboratories is recalling 100 kits of Liquid Protein Calibrators because the assigned value for Rheumatoid Factor over-recovered against the reference material. The calibrator values have been adjusted to re-align to the reference material.

    Product
    Liquid Protein Calibrators (SP CAL (LIQ)) Catalogue Number: IT2691 GTIN: 05055273204032 Product Usage: Liquid Protein Calibrators are intended for in vitro diagnostic use in the calibration of ASO, Complement C3, Complement C4, CRP, Ferritin, Haptoglobin, IgA, IgG, IgM…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0318-2020·2019-11-13

    Zimmer Biomet Recalls Hip Joint Replacement Systems Due to Packaging Adhesion

    Zimmer Biomet is recalling 5.4 million hip joint replacement systems because non-highly polished implants may adhere to the LDPE bag packaging.

    Product
    Various Hip Joint Replacement Systems, Item Nos. 00151504232 00151504432 00151504636 00151504836 00151505040 00151505240 00151505444 00151505644 00151505848 00151506048 00151506248 00151506448 00151506648 00400500060 00401000038 00401000040 00401000041…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0329-2020·2019-11-13

    Zimmer Biomet Recalls Temporary Surgical Devices Due to Packaging Adhesion

    Zimmer Biomet is recalling 5.4 million temporary surgical devices because non-highly polished implants may adhere to the packaging bag.

    Product
    Various temporary devices used during the implantation of the device system: bone fixation plates and screws, drill bits, manual surgical instruments for general use. Item Nos. 0202024301 0202024325 0202024330 0202024342 0202024344 0202024346 0202024360 0202024362…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0308-2020·2019-11-13

    Zimmer Biomet Recalls Periarticular Femur Plates Due to Packaging Adhesion

    Zimmer Biomet is recalling 5,459,583 periarticular femur plates because non-highly polished implants may adhere to the LDPE bag packaging.

    Product
    PERIARTICULAR PLATES - FEMUR, Item Nos. 00234700106 00234700108 00234700110 00234700112 00234700114 00234700116 00234700118 00234700206 00234700208 00234700210 00234700212 00234700214 00234700216 00234700218 00234703104 00234703106 00234703108 00234703204…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0303-2020·2019-11-13

    Sato Pharmaceutical Recalls Sankaijo Botanical Laxative Tablets

    Sato Pharmaceutical Inc. is recalling Sankaijo Botanical Laxative tablets because the sennosides content is lower than the labeled claim.

    Product
    SANKAIJO — SANKAIJO (DOCUSATE SODIUM, SENNOSIDES)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V806000·2019-11-12

    Aston Martin Recalls DB11, Vantage, and DBS Superleggera for Air Bag Defect

    Aston Martin is recalling 2018-2019 DB11, Vantage, and DBS Superleggera vehicles because passenger air bag fasteners may not be tightened properly, increasing injury risk in a crash.

    Product
    ASTON MARTIN — ASTON MARTIN DB11, DBS SUPERLEGGERA, VANTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V805000·2019-11-12

    Ford Recalls 2019-2020 F-150 Trucks for Battery Cable Fastener Issue

    Ford is recalling 2019-2020 F-150 vehicles because a battery cable fastener may loosen, potentially causing engine stalling, loss of braking or steering assist, or fire.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V809000·2019-11-12

    Ford Recalls 2016-2017 Lincoln MKX Vehicles for Battery Cable Fire Risk

    Ford is recalling 2016-2017 Lincoln MKX vehicles with 3.7L engines because the battery cable harness may contact a bracket, causing a short circuit and increasing fire risk.

    Product
    LINCOLN — LINCOLN MKX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E076000·2019-11-12

    Matrix Alpha Motorcycle Helmets Recalled for Retention System Failure

    Matrix Headgear is recalling Alpha motorcycle helmets because the retention system may fail, allowing the helmet to separate from the head during a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V807000·2019-11-08

    Nissan Recalls Murano, Maxima, Pathfinder, QX60 for Brake Fire Risk

    Nissan is recalling 391,479 vehicles because brake fluid may leak onto an electrical circuit board, creating a fire risk.

    Product
    NISSAN — NISSAN, INFINITI MURANO, QX60, MAXIMA, PATHFINDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V804000·2019-11-08

    Mitsubishi i-MiEV Recall for Brake Vacuum Pump Corrosion Risk

    Mitsubishi is recalling 2012-2017 i-MiEV vehicles because water may corrode the brake vacuum pump, causing a loss of braking assist and increasing crash risk.

    Product
    MITSUBISHI — MITSUBISHI I-MIEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-110819·2019-11-08

    USDA Issues Public Health Alert for Ready-to-Eat Entrees Due to Listeria Risk

    USDA FSIS issued a public health alert for specific ready-to-eat entrees containing ingredients recalled by Mann's Packing Co. due to possible Listeria monocytogenes contamination.

    Product
    FSIS Issues Public Health Alert for Ready-to-Eat Entrees due to Possible Listeria Monocytogenes Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V803000·2019-11-07

    Freightliner Cascadia Recall for Brake Chamber Clearance Defect

    Daimler Trucks North America is recalling 2020 Freightliner Cascadia vehicles because brake chambers may contact the frame rail, potentially causing detachment and reduced braking.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V798000·2019-11-07

    NHTSA Recalls 2019 Mercedes-Benz and Freightliner Sprinter Diesel Fuel Systems

    NHTSA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because a fuel system defect may cause diesel leaks or fuel overflow.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 3500, SPRINTER 2500, SPRINTER 4500, SPRINTER 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V802000·2019-11-07

    Hyundai Recalls 2020 Palisade Vehicles for Side Air Bag Defect

    Hyundai is recalling 2020 Palisade vehicles because mounting bolts may damage side curtain air bags, potentially preventing proper inflation in a crash.

    Product
    HYUNDAI — HYUNDAI PALISADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V801000·2019-11-07

    GM Recalls 2014-2016 Chevrolet SS for Steering Connector Corrosion

    General Motors is recalling 2014-2016 Chevrolet SS vehicles because corrosion in the steering connector may cause a loss of electric power steering assist, increasing the risk of a crash.

    Product
    CHEVROLET — CHEVROLET CHEVEROLET SS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V799000·2019-11-07

    Thor Motor Coach Recalls Tuscany and Venetian Motorhomes for Visibility Defect

    Thor Motor Coach is recalling specific Tuscany and Venetian motorhomes because rear reflectors may be positioned too high, reducing vehicle visibility and increasing crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH TUSCANY, TUSCANY XTE, VENETIAN
    Category
    Vehicle
    Distribution
    Distributed nationwide