The Recall Desk

State

Alabama product recalls

73,219 recalls have nationwide distribution and so reach Alabama. 6,371 additional recalls listed Alabama specifically in their distribution scope.

What the numbers show

Total
6,371
Critical
1,131
Severe
1,349
Most recent
2026-10-06

Of the 6,371 recalls naming Alabama we have scored against our rubric, 1,131 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,349 (21%) are Severe.

These figures cover only the 6,371 recalls whose distribution notice names Alabama specifically. The 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

15026–15050 of 79590

  • HighFDA (Devices)·Z-2624-2023·2023-09-27

    FDA Recalls ALKP Chemistry Analyzer Slides for Potential Diagnostic Errors

    Ortho-Clinical Diagnostics is recalling VITROS XT Chemistry ALKP Slides worldwide because high alkaline phosphatase samples may cause the analyzer to report falsely low results, potentially missing or delaying liver disease diagnoses.

    Product
    VITROS XT Chemistry Products ALKP Slides
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2598-2023·2023-09-27

    Stryker ACM Advanced Cement Mixing System Nozzle May Disassemble

    Stryker is recalling the ACM bone cement mixing system because the break-away femoral nozzle may disassemble or break off during surgery, potentially causing loss of device function and components to fall into the surgical site.

    Product
    Stryker ACM (Advanced Cement Mixing) System: ACM Kit w/ Femoral Breakaway Nozzle-Allows the user to mix bone cement witha constant high vacuum through the process Catalog Number: 0306-563-000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2625-2023·2023-09-27

    Philips Tempus Pro Patient Monitor Software Error Impairs Critical Monitoring

    Certain Philips Tempus Pro Patient Monitors may display an error message when laryngoscopes are disconnected, requiring a 60-100 second restart that prevents vital sign monitoring and airway visualization during intubation. This may lead to treatment delays or hypoxia.

    Product
    Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, and 00-1007, when Used With Tempus Pro Video Laryngoscope, REF 01-2044
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-2594-2023·2023-09-27

    SofTech Wheelchair Cushions Recalled for Defective Battery Overheating Risk

    Aquila Corporation is recalling 134 SofTech Pressure-Sensing Wheelchair Cushions with defective battery packs that can overheat, risking property damage and a possible injury. The affected units have been distributed nationwide in the US and internationally to Canada, Sweden, Romania, Australia, and the UK.

    Product
    SofTech Pressure-Sensing Wheelchair Cushions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1176-2023·2023-09-27

    Sunscreen Recall: Humanrace Ozone Body Protection Cream Lacks Declared SPF

    Humanrace Suncare Ozone Body Protection Cream SPF 30 does not contain the sun protection factor declared on the label. Approximately 2,942 units have been recalled.

    Product
    Humanrace Suncare, Ozone Body Protection Cream, Broad Spectrum Sunscreen SPF 30, packaged as a 148mL (5 fl oz.) bottle, PA ++++, 100% mineral, Active Ingredient: Zinc oxide 15%, Snow Mushroom, Squalene, Aloe, Dist. By: @Humanrace 2022 Beverly Hills, CA 90210, USA, NDC 82779-002
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2592-2023·2023-09-27

    Sentec Membrane Changer components recalled for manufacturing defect

    SenTec AG recalls Membrane Changer components for the Sentec Digital Monitoring System due to a potential manufacturing defect that could affect measurement accuracy.

    Product
    Membrane Changer Single-Use, REF MC, each package contains 3 changers; Membrane Changer Reloadable, REF MC-R, each package contains 3 changers; and Membrane Changer Insert, REF MC-I, each package contains 5 inserts. All are components of the Sentec Digital Monitoring System…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2590-2023·2023-09-27

    Arrow ErgoPack PICC Catheters Recalled for Incorrect Product Labeling

    Arrow International is recalling 190 units of Arrow ErgoPack One-Lumen PICC catheters (Lot 13F22J0617) because the product code and product name were incorrectly printed on the kit packaging. The units were distributed nationwide.

    Product
    Arrow ErgoPack Pressure Injectable One-Lumen PICC, REF CDC-05541-HPK1A; catheter, intravascular
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1524-2023·2023-09-27

    Giant Eagle Cheese Spread Recalled Due to Inconsistent Refrigeration Labels

    Giant Eagle Easy Melt cheese spread products have inconsistent refrigeration instructions on their labels. The varying label requirements may cause improper storage, creating potential food safety concerns.

    Product
    giant eagle Easy Melt, Pasteurized Prepared Cheese Spread. Net Wt 32 oz (2lb)907g. UPC 0 30034-06289 7. Refrigerate after Opening. Distributed by Giant Eagle, Inc., Pittsburgh, PA 15328-2809.
    Category
    Food
    Distribution
    32 states
  • ModerateFDA (Food)·F-1530-2023·2023-09-27

    HEB Easy Melt Pasteurized Cheese Spread Recalled for Conflicting Refrigeration Labels

    Great Lakes Cheese is recalling HEB Easy Melt Original Pasteurized Process Cheese Spread because refrigeration instructions vary across product labels. No illnesses have been reported.

    Product
    Pasteurized Process Cheese Spread packaged under the following brands and sizes: 1. HEB Easy Melt Original, Net Wt 16 oz (1 lb) 453g. UPC 0 41220-73808 3. Refrigerate after Opening. Made with Pride and Care for H-E-B, San Antonio, Texas 78204 2. HEB Easy Melt Original…
    Category
    Food
    Distribution
    32 states
  • ModerateFDA (Food)·F-1526-2023·2023-09-27

    Refrigerated Cheese Products Recalled for Conflicting Label Instructions

    Great Lakes Cheese is recalling multiple brands of refrigerated pasteurized cheese products due to conflicting refrigeration instructions on product labels. The conflicting label requirements could lead to improper storage.

    Product
    Pasteurized Prepared Cheese Product, packaged under the following brands and sizes: 1. Clancy's CheeseMelt, 1/2 Less Fat Than Cheddar Cheese, Net Wt 32 oz (2 lbs) 907g. Refrigerate after Opening. Dist, & Sold exclusively by: Aldi, Batavia, IL 60510 2. Dutch Farms Cheese…
    Category
    Food
    Distribution
    32 states
  • ModerateFDA (Food)·F-1527-2023·2023-09-27

    Great Value Cheese Recall Due to Inconsistent Refrigeration Label Requirements

    Great Value Melt'n Dip Easy Melt Cheese is being recalled due to inconsistent refrigeration labeling requirements that may result in improper storage. The product has a use-by date of 1/4/2024 or earlier.

    Product
    Great Value Melt'n Dip Easy Melt Cheese, Reduced Fat Pasteurized Prepared Cheese Product, Net Wt 32 oz (2 lbs) 907g. UPC 0 78742-01517 0. Refrigerate after Opening. Distributed By: Walmart Inc., Bentonville, AR 72716
    Category
    Food
    Distribution
    32 states
  • ModerateFDA (Food)·F-1525-2023·2023-09-27

    Pasteurized Process Cheese Spread Recalled for Conflicting Refrigeration Labels

    Great Lakes Cheese and related brands recalled 7.2 million pounds of pasteurized cheese spread due to conflicting refrigeration instructions on labels that may prevent proper storage.

    Product
    Pasteurized Process Cheese Spread packaged under the following brands and sizes: 1. Great Lakes Cheese Easy Cheesy, Net Wt 32 oz (2lb)907g. UPC 0 36514-19245 0. Refrigerate After Purchase. Distributed by Great Lakes Cheese Co., Inc. Hiram, OH 44234 2. HEB Easy Melt Queso…
    Category
    Food
    Distribution
    32 states
  • ModerateFDA (Food)·F-1532-2023·2023-09-27

    Refrigerated Cheese Products Recalled for Unclear Refrigeration Label Requirements

    Great Lakes Cheese, Inc. is recalling refrigerated cheese products because product labels have varying refrigeration requirements that could lead to improper storage. Approximately 7.2 million lbs of products sold under Clancy's and Hill Country Fare brands are affected.

    Product
    Pasteurized Prepared Cheese Product, Queso Blanco, Half the Fat of Cheddar Cheese packaged under the following brands and sizes: 1. Clancy's CheeseMelt, Net Wt 32 oz (2 lbs) 907g. Refrigerate after Opening. Dist, & Sold exclusively by: Aldi, Batavia, IL 60510 2. Hill…
    Category
    Food
    Distribution
    32 states
  • ModerateFDA (Food)·F-1531-2023·2023-09-27

    Pasteurized Cheese Product Recalled for Inconsistent Refrigeration Instructions on Labels

    Great Lakes Cheese, Inc. is recalling Hill Country Fare Melt'n Cheese because product labels contain inconsistent refrigeration requirements, which may result in improper storage by consumers.

    Product
    Hill Country Fare Melt'n Cheese, Pasteurized Prepared Cheese Product, Net Wt 32 oz (2 lbs) 907g. UPC 0 41220-77273 5. Refrigerate after Opening. Distributed By: H-E-B, San Antonio, TX 78204
    Category
    Food
    Distribution
    32 states
  • ModerateFDA (Food)·F-1533-2023·2023-09-27

    HEB Easy Melt Salsa Queso Recalled Due to Conflicting Refrigeration Labels

    HEB Easy Melt Salsa Queso is recalled for conflicting refrigeration labels that may cause improper storage. Over 7.2 million pounds were distributed across 32 states.

    Product
    HEB Easy Melt Salsa Queso, with Tomatoes, Jalapeno Peppers & Onions, Net Wt 32 oz (2 lbs) 907g. UPC 0 41220-33063 8. Refrigerate after Opening. Made with Pride and Care for H-E-B, San Antonio, Texas 78204
    Category
    Food
    Distribution
    32 states
  • ModerateFDA (Food)·F-1528-2023·2023-09-27

    Refrigerated Pasteurized Cheese Products Recalled Due to Labeling Inconsistency

    Great Value and SE Grocers refrigerated cheese products are being recalled because labels contain inconsistent refrigeration requirements, which may result in improper storage by consumers.

    Product
    Pasteurized Prepared Cheese Product packaged under the following brands and sizes: 1. Great Value Original Melt'n Dip Easy Melt Cheese, Net Wt 16 oz (1 lb) 453g. UPC 0 78742-01512 5. Refrigerate after Opening. Distributed By: Walmart Inc., Bentonville, AR 72716 2.…
    Category
    Food
    Distribution
    32 states
  • ModerateFDA (Drugs)·D-1168-2023·2023-09-27

    ChloraPrep One-Step Topical Applicators Recalled for Unsupported Shelf-Life Claims

    BD ChloraPrep One-Step topical applicators are recalled because the 36-month shelf life is not supported by stability data; the product may develop fungal contamination beyond 12 months.

    Product
    CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1529-2023·2023-09-27

    Harris Teeter Cheesy Melt recalled for labeling refrigeration requirements

    Harris Teeter Cheesy Melt pasteurized cheese product is recalled because labeling variations may prevent proper refrigeration. Approximately 7.2 million pounds are affected across 31 states with use-by dates of March 8, 2024 and earlier.

    Product
    Harris Tetter Cheesy Melt, Pasteurized Prepared Cheese Product, Net Wt 32 oz (2 lbs) 907g. UPC 0 72036-70682 9. After Opening, Refrigerate Up to 8 weeks. Do Not Freeze. Proudly Distributed By: Harris Teeter, LLC, Matthews, NC 28105
    Category
    Food
    Distribution
    32 states
  • ModerateFDA (Drugs)·D-1172-2023·2023-09-27

    Cequa cyclosporine ophthalmic solution recalled nationwide for subpotency

    Sun Pharmaceutical is recalling Cequa (cyclosporine) ophthalmic solution because certain lots contain less active ingredient than specified. Contact your doctor if using an affected product.

    Product
    CEQUA — CEQUA (CYCLOSPORINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1523-2023·2023-09-27

    Cheese Spread Products Recalled for Inconsistent Refrigeration Requirements

    Multiple cheese spread brands are being recalled due to inconsistent refrigeration instructions on labels. Consumers should verify proper storage and discard products with unclear label instructions.

    Product
    Cheese Spread Pasteurized Process packaged under the following brands and sizes: 1. bowl & Basket, A Shoprite Brand, Net Wt 32 oz (2lb)907g. UPC 0 41190-46935 2. Refrigerate after Opening. Distributed by: Wakeforn Food Corp, 5000 Riverside Drive, Keasbey, NJ 08832 2.…
    Category
    Food
    Distribution
    32 states
  • LowFDA (Devices)·Z-2591-2023·2023-09-27

    Arrow ErgoPack PICC catheter kits recalled for incorrect product labeling

    Arrow International recalled 177 ErgoPack PICC catheter kits because the product code and name were incorrectly listed on the packaging. No illnesses or injuries reported.

    Product
    Arrow ErgoPack, Pressure Injectable Two-Lumen PICC pre-loaded with Arrow VPS Stylet, REF CDC-35552-VPS; Catheter: Percutaneous, implanted, long-term intravascular catheter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·046-2023·2023-09-25

    USDA Recalls Ineligible Imported Pork Chicharrones from Honduras

    Del Valle Import and Export is recalling 1,271 pounds of pork chicharrones imported from Honduras, a country ineligible to export pork to the U.S.

    Product
    Del Valle Import and Export, LLC, Recalls Ineligible Pork Chicharrones Product Imported From Honduras
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·23V652000·2023-09-25

    Kia Recalls Multiple Models Due to Electrical Short Fire Risk

    Kia is recalling 1.7 million vehicles because an electrical short in the brake control unit may cause an engine compartment fire.

    Product
    KIA — KIA SORENTO, RIO, OPTIMA HYBRID, SOUL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V651000·2023-09-22

    Hyundai Recalls Multiple Models Due to ABS Module Fire Risk

    Hyundai is recalling over 1.6 million vehicles because a leaking ABS module may cause an engine compartment fire. Owners should park outside until the repair is complete.

    Product
    HYUNDAI — HYUNDAI ELANTRA, AZERA, SANTA FE, GENESIS COUPE
    Category
    Vehicle
    Distribution
    Distributed nationwide