The Recall Desk

State

Alabama product recalls

73,741 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.

These figures cover only the 6,377 recalls whose distribution notice names Alabama specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35651–35675 of 80118

  • SevereFDA (Drugs)·D-1507-2019·2019-07-31

    Pharma-Natural Recalls Workvie Pain Roll-On for Manufacturing Violations

    Pharma-Natural Inc. is recalling Workvie Instant Pain Relieving Roll On due to current good manufacturing practice deviations, including lack of process and cleaning validation.

    Product
    Workvie Instant Pain Relieving Roll On (Lidocaine HCL 4% + Menthol 1% & Arnica), 2.5oz (71 g) roll on bottle, Exclusively Distributed by: Marketite, LLC., Coral Gables, FL 33134, NDC 72393-201-25.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1587-2019·2019-07-31

    Brand Castle Recalls Hot Cocoa Cookie Mix Due to E. coli Risk

    Brand Castle LLC is recalling Hot Cocoa Cookie Mix because a supplier reported potential E. coli contamination in the flour used.

    Product
    Hot Cocoa Cookie Mix, 22.9 oz glass jar, 6/case
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Food)·F-1584-2019·2019-07-31

    Brand Castle Brownie Mix Recalled for Potential E. coli Contamination

    Brand Castle LLC is recalling Billion Dollar Brownie Mix due to potential E. coli contamination in flour. The product was distributed in ten states.

    Product
    Billion Dollar Brownie Mix, 28.3 oz glass jar, 6/case
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Drugs)·D-1528-2019·2019-07-31

    Gordon Laboratories Recalls MONSEL'S Solution Due to Microbial Contamination

    Gordon Laboratories is recalling 277 boxes of MONSEL'S (Ferric Subsulfate) Solution due to microbial contamination and high iron content.

    Product
    MONSEL'S (Ferric Subsulfate) Solution, 8 mL amber glass bottle, packaged as one dozen bottles with applicators per box, Rx only, Gordon Laboratories, Upper Darby, PA 19082, NDC 10481-0112-8.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1517-2019·2019-07-31

    Tris Pharma Recalls Hydrocodone and Chlorpheniramine Suspension Due to Potency Issues

    Tris Pharma is recalling 2,550 bottles of Hydrocodone Polistirex and Chlorpheniramine Polistirex Extended-Release Suspension due to high out-of-specification results for active ingredients and preservatives.

    Product
    HYDROCODONE POLISTIREX AND CHLORPHENIRAMINE POLISTIREX — HYDROCODONE POLISTIREX AND CHLORPHENIRAMINE POLISTIREX (HYDROCODONE POLISTIREX AND CHLORPHENIRAMINE POLISTIREX)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1522-2019·2019-07-31

    Geritrex Recalls Gericare Diocto Liquid Stool Softener Due to Microbial Contamination Risk

    Geritrex, LLC is recalling 6,165 bottles of Gericare Diocto Liquid Stool Softener due to cGMP deviations that may result in microbial contamination.

    Product
    Gericare Diocto Liquid Docusate Sodium Stool Softener, 50 mg/5mL, 16 FL OZ (473 ml), Dist. BY: Gericare Pharmaceuticals corp. 1650 63rd Street Brooklyn, NY 11204, NDC 57896-403-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1967-2019·2019-07-31

    PROBAR Meal Wholeberry Blast bars recalled for potential undeclared milk and soy allergens

    The FDA is recalling PROBAR Meal Wholeberry Blast bars because they may contain undeclared milk and soy ingredients. Consumers should discard affected bars and consult their healthcare provider if allergic.

    Product
    PROBAR MEAL Wholeberry Blast, Net Wt. 3oz.(85g), Film wrapped bar
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1525-2019·2019-07-31

    Geritrex Recalls Ritussin DM Due to Potential Microbial Contamination

    Geritrex, LLC is recalling Ritussin DM Double Strength cough syrup due to cGMP deviations that may result in microbial contamination.

    Product
    Ritussin DM Double Strength, 4 FL. OZ. (118 mL), RIJ Pharmaceutical Corporation 40 Commercial Avenue Middletown, NY 10941
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V563000·2019-07-31

    BMW Recalls 2018-2019 X3 and X4 Models for Seatback Welding Defect

    BMW is recalling 2018-2019 X3 and 2019 X4 vehicles because improperly welded front seatback frames may fold unexpectedly, increasing injury risk in a crash.

    Product
    BMW — BMW X3, X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1524-2019·2019-07-31

    Geritrex Recalls Iron Elixir Due to Potential Microbial Contamination

    Geritrex, LLC is recalling Preferred Plus Pharmacy Iron Elixir due to cGMP deviations that may result in microbial contamination.

    Product
    Preferred Plus Pharmacy Iron Elixir Ferrous Sulfate, 220 mg, 16 fl oz. (473 mL), Distributed by: Geri-care Pharmaceuticals Corp. 1650 63rd Street Brooklyn, NY 11204, NDC 52807-177-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1521-2019·2019-07-31

    Geritrex Recalls Ritussin DM Due to Potential Microbial Contamination

    Geritrex, LLC is recalling 5,107 bottles of Ritussin DM Children & Adults due to cGMP deviations that may result in microbial contamination.

    Product
    Ritussin DM Children & Adults, 4 Fl. Oz. (118 mL), RIJ Pharmaceutical Corporation 40 Commercial Avenue Middletown, NY 10941, NDC 53807-409-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1527-2019·2019-07-31

    Geritrex Recalls Preferred Plus Dioctyl Liquid Stool Softener Due to Microbial Contamination

    Geritrex, LLC is recalling Preferred Plus Dioctyl Liquid Stool Softener due to cGMP deviations that may result in microbial contamination.

    Product
    Preferred Plus Dioctyl Liquid Stool Softener (Docusate Sodium), 50mg/5mL, 16 FL. Oz. (1 PT.) 473 mL, Manufactured by RIJ Pharmaceutical Corp. 40 Commercial Avenue Middletown, NY 10941, Distributed by Kinray Inc. Whitestone, NY 11357, NDC 53807-216-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1498-2019·2019-07-31

    Pharma-Natural Recalls Double Tussin DM Due to Manufacturing Violations

    Pharma-Natural Inc. is recalling 500 bottles of Double Tussin DM because the product was manufactured with current good manufacturing practice violations.

    Product
    DOUBLE TUSSIN DM (Dextromethorphan Hbr 20 mg, Guaifenesin 300 mg) in each 5ml teaspoon, 4 FL OZ (120 mL) bottle, Distributed by: Pamby Dist., Miami, FL 33414, NDC 63708-121-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1526-2019·2019-07-31

    Gericare Geri-Tussin DM Recalled for Potential Microbial Contamination

    Geritrex, LLC is recalling Gericare Geri-Tussin DM due to cGMP deviations that may result in microbial contamination.

    Product
    Gericare Geri-Tussin DM, 16 FL OZ (473 mL), Geri-care Phamaceuticals Corp. 1650 63rd Street Brooklyn, NY, NDC 57896-660-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1520-2019·2019-07-31

    Geritrex Recalls Diphenhydramine Oral Liquid Due to Potential Microbial Contamination

    Geritrex, LLC is recalling 8,645 bottles of Diphenhydramine Oral Liquid due to cGMP deviations that may result in microbial contamination.

    Product
    Diphenhydramine Oral Liquid Alcohol Free, 12.5 mg/5 mL, 4 fl oz (118 mL), RIJ Pharmaceutical Corporation 40 Commercial Avenue Middletown, NY 10941, NDC 53807-204-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1965-2019·2019-07-31

    Probar Meal Superfood Slam Bars Recalled for Undeclared Milk and Soy

    Probar LLC is recalling 2,908 Superfood Slam meal bars nationwide and in Canada due to undeclared milk and soy allergens.

    Product
    PROBAR MEAL Superfood Slam, Net Wt. 3oz.(85g), Film wrapped bar
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1969-2019·2019-07-31

    Probar Chocolate Coconut Bars Recalled for Undeclared Milk and Soy

    Probar LLC is recalling 2,016 Chocolate Coconut bars because they may contain undeclared milk and soy allergens.

    Product
    PROBAR The Simply Real Bar: Chocolate Coconut, Net Wt. 85g, Film wrapped bar
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1582-2019·2019-07-31

    Brand Castle Recalls Grinch Sugar Cookie Mix Due to E. coli Risk

    Brand Castle LLC is recalling The Grinch Sugar Cookie Mix with Sprinkles because a supplier reported potential E. coli contamination in the flour used.

    Product
    The Grinch Sugar Cookie Mix with Sprinkles, 22.3 oz glass jar, 6/case
    Category
    Food
    Distribution
    10 states