The Recall Desk

State

Alabama product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50101–50125 of 80202

  • ModerateFDA (Devices)·Z-0394-2017·2016-11-16

    Becton Dickinson Recalls Spinal Anesthesia Trays Containing Recalled Lidocaine

    Becton Dickinson is recalling specific BD Spinal Anesthesia Trays because they contain Hospira 5% Lidocaine HCI ampules that are subject to a separate recall.

    Product
    catalog # 405612 BD Spinal Anesthesia Tray 22G x 3.5 in. BD" Quincke Spinal Needle Lidocaine HCL (5%) with Dextrose (7.5%), 2 mL catalog # 405622 BD Spinal Anesthesia Tray 25G x 3.5 in. BD" Quincke Spinal Needle Bupivacaine HCL (0.75%) with Dextrose (8.25%), 2 mL…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0368-2017·2016-11-16

    Zimmer Air Dermatome II Handpiece Recalled for Surface Coating Defects

    Zimmer Biomet Surgical is recalling Air Dermatome II Handpiece loaners because the surface coating may blister, peel, or discolor over time. No injuries have been reported.

    Product
    Zimmer¿ Air Dermatome II Handpiece Loaner, item number 01-8851-001-00. Device is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which is then…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0366-2017·2016-11-16

    FDA Recalls Custom Packaging for Devon Light Gloves

    The FDA is recalling custom packaging for Devon Light Gloves due to added instructions for use regarding barrier integrity inspection.

    Product
    Professional Hospital Supply, Inc Custom Packaging containing the Devon Light Glove Item Number Description 380789003 SURE SET SINGLE BASIN PACK 400383006 MAJOR BASIN PACK…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0328-2017·2016-11-16

    Rich Products Recalls Chocolate Iced Éclairs for Plastic Foreign Material

    Rich Products Corp is recalling specific lots of New York Style Chocolate Iced Éclairs due to the potential presence of plastic foreign material.

    Product
    New York Style Chocolate Iced ¿clairs under the following labels: 1) Richs New York Style Chocolate Iced ¿clairs, NET WT 8 oz (226g) (UPC Code:049800147799), 2) Bakery Fresh Goodness NY Style Chocolate ¿clairs, NET WT 8 oz (226g) (UPC Code:011110456601), 3) Food Lion NY Style…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0365-2017·2016-11-16

    FDA Recalls Covidien Devon Light Glove Sub-Assembly for Added Instructions

    The FDA is recalling 118,800 units of the Covidien Devon Light Glove sub-assembly to add instructions for use regarding barrier integrity inspection.

    Product
    Covidien Devon Light Glove sub-assembly non-sterile For Kit Packers Product Usage: A disposable, sterile, single-use cover for compatible surgical light handles
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0379-2017·2016-11-16

    Abbott Recalls Architect Lactic Acid Assay Due to Drug Interference

    Abbott is recalling 26,837 kits of the ARCHITECT Lactic Acid assay because the drug N-Acetyl Cysteine causes negative interference with the reagent.

    Product
    ARCHITECT Lactic Acid Part # 09D891T21 The Lactic Acid assay is used for the quantitation of lactic acid in human plasma.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0364-2017·2016-11-16

    FDA Adds Instructions for Use to Covidien Devon Light Glove Recall

    The FDA is adding instructions to inspect the barrier integrity of the Covidien Devon Light Glove after application. This affects sterile surgical kits distributed in the US and abroad.

    Product
    Covidien Devon Light Glove packaged in sterile surgical kits Reference: 31140208 Product Usage: A disposable, sterile, single-use cover for compatible surgical light handles
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0372-2017·2016-11-16

    Schaerer Surgical Table Floor Locking Cylinders Recalled for Leak Risk

    Schaerer Medical USA Inc is recalling replacement floor locking cylinders for model 7300 surgical tables because they may leak due to an incorrect O-ring.

    Product
    Replacement floor locking cylinders for the Schaerer model 7300 surgical tables. Replacement cylinders are part number 85118. Product Usage: The cylinders are used to lock the surgical table in place.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0369-2017·2016-11-16

    Medimaps TBS iNsight Software Recalled for Incorrect FRAX Calculations

    Medimaps Group is recalling TBS iNsight v.3.0.1 software because FRAX values are incorrect when specific spine scan conditions are met.

    Product
    TBS iNsight Version v.3.0.1 Product Usage: TBS iNsight is a medical device software that is installed on bone densitometers for analysis of bone microarchitecture and osteoporosis management.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0371-2017·2016-11-16

    Schaerer 7300 Surgical Tables Recalled for Defective Floor Locking Cylinders

    Schaerer Medical USA Inc is recalling four 7300 model surgical tables because defective floor locking cylinders may leak due to incorrect O-rings.

    Product
    The surgical table is a stand alone unit. Three (3) floor locking cylinders are attached to the base of the surgical table. The individual cylinders are replaceable. Product Usage: The cylinders are used to lock the surgical table in place.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0135-2017·2016-11-16

    Mylan Recalls Clonazepam Tablets Due to Impurity Specification Failure

    Mylan Institutional, Inc. is recalling specific lots of Clonazepam Tablets, USP, 0.5 mg because they failed impurity specifications.

    Product
    Clonazepam Tablets, USP, 0.5 mg, packaged in a)100- count unit dose box of 10 x 10 blister cards (NDC 51079-881-20) and b) 300-count unit dose box of 10 x 30 punch cards (NDC 51079-881-56), Rx only, Manufactured by Mylan Pharmaceuticals Inc, Morgantown, WV, 26505
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0136-2017·2016-11-16

    Mylan Recalls Clonazepam Tablets Due to Impurity Specification Failure

    Mylan Institutional is recalling specific lots of Clonazepam 1.0 mg tablets because a known impurity exceeded specification limits during stability testing.

    Product
    Clonazepam Tablets, USP, 1.0 mg, packaged in a 100- count unit dose box of 10 x 10 blister cards, Rx only, Manufactured by Mylan Pharmaceuticals Inc, Morgantown, WV, 26505, NDC 51079-882-20
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0134-2017·2016-11-16

    Taro Recalls Kamedis Dandruff Care Kits Due to Low Active Ingredient

    Taro Pharmaceuticals is recalling 17,100 kits of Kamedis Bio-Herbal Dandruff Care System because the active ingredient, zinc pyrithione, was found to be subpotent.

    Product
    Kamedis BIO-HERBAL DANDRUFF CARE THERAPEUTIC 2-STEP DANDRUFF CARE SYSTEM - Kamedis Bio-Herbal Dandruff Care 0.1% PYRITHIONE ZINC, STEP 1 PRE-TREAT Concentrated Botanical Scalp Lotion (0.1% Pyrithione Zinc) 4.20 FL OZ (125mL) (NDC 51672-2126-0) and STEP 2 CLEANSE Concentrated…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V826000·2016-11-15

    Newmar Recalls 2016-2017 Dutch Star and Ventana Motorhomes for Fire Risk

    Newmar is recalling 370 model year 2016-2017 Dutch Star and Ventana motorhomes because a power steering hose may rub against the starter motor, causing electrical arcing and a fire risk.

    Product
    NEWMAR — NEWMAR DUTCH STAR, VENTANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V827000·2016-11-15

    Entegra Recalls 2017 Motorhomes Due to Throttle Wire Interference

    Entegra is recalling 2017 Aspire, Anthem, Cornerstone, and Insignia motorhomes because throttle wires may not be twisted, causing unintended acceleration or deceleration.

    Product
    ENTEGRA — ENTEGRA CORNERSTONE, ANTHEM, ASPIRE, INSIGNIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V828000·2016-11-15

    Forest River Recalls Motorhomes and Toyhaulers Due to Ladder Hinge Defect

    Forest River is recalling specific 2013-2017 motorhomes and toyhaulers because aluminum ladder hinges may separate, causing the ladder to fall and increasing injury risk.

    Product
    FOREST RIVER — FOREST RIVER, PALOMINO, PRIME TIME FR3, COLUMBUS, XLR, SPARTAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V823000·2016-11-15

    KZRV Recalls 2015 Trailers Due to Ladder Hinge Separation Risk

    KZRV is recalling 2015 Venom, Inferno, Sportsmen, Sportster, MXT, and SportTrek trailers because aluminum ladder hinges may separate, causing the ladder to fall and increasing injury risk.

    Product
    KZRV — KZRV SPORTSTER, VENOM, SPORTSMEN, MXT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V825000·2016-11-15

    Keystone RV Recalls Fifth Wheels Due to Ladder Hinge Defect

    Keystone RV is recalling 2015-2016 fifth wheels because aluminum ladder hinges may separate, causing the ladder to fall and increasing injury risk.

    Product
    KEYSTONE — KEYSTONE, DUTCHMEN CARBON, FUZION, RAPTOR, VOLTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V824000·2016-11-15

    Freightliner Trucks Recalled for Potential Tire Tread Separation

    Daimler Trucks North America is recalling 2017 Freightliner trucks because improperly cured tires may separate, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2, CASCADIA, 122SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V822000·2016-11-14

    Keystone Recalls 2017 Cougar Fifth Wheel Trailers for Propane Leak Risk

    Keystone RV Company is recalling specific 2017 Cougar fifth wheel trailers because a propane manifold may contact floor fasteners, creating a potential leak and fire hazard.

    Product
    KEYSTONE — KEYSTONE COUGAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V819000·2016-11-14

    Heartland Recalls 2015-2016 Trailers Due to Ladder Hinge Defect

    Heartland is recalling 2,045 travel trailers because aluminum ladder hinges may separate, causing the ladder to fall and increasing injury risk.

    Product
    HEARTLAND — HEARTLAND ROAD WARRIOR, CYCLONE, TORQUE
    Category
    Vehicle
    Distribution
    Distributed nationwide