The Recall Desk

State

Alabama product recalls

73,809 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.

These figures cover only the 6,378 recalls whose distribution notice names Alabama specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42301–42325 of 80187

  • SevereFDA (Drugs)·D-0719-2018·2018-05-02

    Coastal Meds Recalls Hydroxocobalamin Injectable Due to Particulate Matter

    Coastal Meds, LLC. is recalling 1,506 vials of Hydroxocobalamin Injectable due to the presence of unknown particulate matter. The product was distributed nationwide.

    Product
    HYDROXOCOBALAMIN Injectable-30 mL MDV. Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1127-2018·2018-05-02

    Seabear Recalls Cold Smoked Coho Salmon Lox Due to Salt Deviations

    Seabear Company is recalling 2,080 units of Cold Smoked Wild Coho Salmon Lox due to water phase salt deviations and mislabeled storage instructions.

    Product
    Cold Smoked Wild Coho Salmon Lox , Gerard & Dominique Seafoods brand, Reduced Oxygen Packaging, Net Wt. 3 oz (85g). UPC 7 52047 92635 4. The package label of the Cold Smoked Coho Salmon bears this instructions "***KEEP REFRIGERATED AT OR BELOW 38 F***". The master case…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0699-2018·2018-05-02

    Premier Pharmacy Labs Recalls Morphine Sulfate Injection Due to Sterility Concerns

    Premier Pharmacy Labs is recalling specific lots of Morphine Sulfate Injection because routine testing of other lots detected microbial contamination risks.

    Product
    Morphine Sulfate 2 mg/mL PF Injection. 1 mL in a 3ml Sterile Single-Dose Syringe. 8265 Commerical Way Weeki Wachee, FL 34613. NDC 69623-129-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0726-2018·2018-05-02

    Coastal Meds Recalls Pyridoxine Injectable Due to Particulate Matter

    Coastal Meds, LLC. is recalling 635 vials of Pyridoxine Injectable due to the presence of unknown particulate matter.

    Product
    PYRIDOXINE Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1134-2018·2018-05-02

    Nxtgen Botanicals Maeng Da Kratom Recalled for Salmonella Risk

    NGB Corp is recalling Nxtgen Botanicals Maeng Da Kratom dietary supplements due to potential Salmonella contamination.

    Product
    Nxtgen Botanicals, Maeng Da Kratom, Dietary Supplement, 70 capsules
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0724-2018·2018-05-02

    Coastal Meds Recalls LIPO-PLEX Injectable Due to Particulate Matter

    Coastal Meds, LLC. is recalling LIPO-PLEX Injectable-30 mL vials nationwide due to the presence of unknown particulate matter.

    Product
    LIPO-PLEX Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0700-2018·2018-05-02

    Premier Pharmacy Labs Recalls Morphine Sulfate Syringes Due to Sterility Concerns

    Premier Pharmacy Labs Inc is recalling 4,192 syringes of Morphine Sulfate 4 mg/mL PF Injection due to a lack of assurance of sterility.

    Product
    Morphine Sulfate 4 mg/mL PF Injection. 1 mL in a 3ml Sterile Single-Dose Syringe. 8265 Commerical Way Weeki Wachee, FL 34613. NDC 69623-127-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1532-2018·2018-05-02

    BD Vacutainer Push Button Blood Collection Set Recalled for Sterility Issues

    Becton Dickinson is recalling BD Vacutainer Push Button Blood Collection Sets because they do not meet the labeled sterility assurance level.

    Product
    BD Vacutainer¿ Push Button Blood Collection Set 0.8 x 19 mm x 305 mm 21G x ¿ x 12 Catalog 367344
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V285000·2018-05-02

    Thor Motor Coach Recalls Tuscany and Venetian Motorhomes for Fire Risk

    Thor Motor Coach is recalling 2011-2017 Tuscany and Venetian motorhomes because an incorrectly routed power steering hose may cause electrical arcing and a fire.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH VENETIAN, TUSCANY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1126-2018·2018-05-02

    Seabear Hot Smoked Keta Salmon Recalled for Salt Deviations and Mislabeling

    Seabear Company is recalling 381 units of Hot Smoked Keta Beergarden Salmon due to water phase salt deviations and mislabeled storage instructions.

    Product
    Hot Smoked Keta Beergarden Salmon, Seabear brand, Reduced Oxygen Packaging, Net Wt. 4oz (113g). No UPC.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0701-2018·2018-05-02

    Premier Pharmacy Labs Recalls Hydromorphone Syringes Due to Sterility Concerns

    Premier Pharmacy Labs is recalling 3,570 hydromorphone syringes because routine testing of other lots found microbial contamination risks.

    Product
    Hydromorphone HCl 1 mg/mL PF INJ. 1mL in a 3mL Sterile Single-Dose Syringe. 8265 Commercial Way Weeki Wachee, FL 34613 NDC 69623-249-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V284000·2018-05-02

    Volkswagen Atlas Recall for Fuel Tank Leak Fire Risk

    Volkswagen is recalling 2018 Atlas vehicles because a manufacturing error may cause the fuel tank to leak, increasing the risk of a fire.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0722-2018·2018-05-02

    FDA Recalls Lipoderm Extreme Injectable Due to Particulate Matter

    Coastal Meds, LLC. is recalling 3,733 vials of LIPO-DEN EXTREME Injectable-30 mL due to the presence of unknown particulate matter.

    Product
    LIPO-DEN EXTREME Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0718-2018·2018-05-02

    Coastal Meds Recalls ADENO-PLEX Injectable Due to Particulate Matter

    Coastal Meds, LLC. is recalling 200 vials of ADENO-PLEX Injectable-30 mL MDV due to the presence of unknown particulate matter.

    Product
    ADENO-PLEX Injectable-30 mL MDV. Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0702-2018·2018-05-02

    Premier Pharmacy Labs Recalls NeoStigmine Syringes Due to Sterility Concerns

    Premier Pharmacy Labs is recalling NeoStigmine Methylsulfate syringes because routine testing of other lots detected microbial contamination risks.

    Product
    NEOstigmine Methylsulfate (1 mg/mL) 3mg per 3mL. 3mL Single Dose Syringe. Premier Pharmacy Labs. 8265 Commercial Way Weeki Wachee, FL 34613 NDC 69623-234-14.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0723-2018·2018-05-02

    Coastal Meds Recalls LIPO-DEN PLUS Injectable Due to Particulate Matter

    Coastal Meds, LLC. is recalling 1,457 vials of LIPO-DEN PLUS Injectable because of the presence of unknown particulate matter. The product was distributed nationwide in the USA.

    Product
    LIPO-DEN PLUS Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0697-2018·2018-05-02

    Bayer Recalls Alka-Seltzer Plus Packages Due to Ingredient Label Mismatch

    Bayer is recalling specific Alka-Seltzer Plus packages because the ingredients listed on the front sticker may not match the actual product inside the carton.

    Product
    All Alka-Seltzer Plus¿ packages with a full front panel instant Redeemable Coupon (IRC) affixed to the individual carton. The recalled products can be identified by checking the Bayer logo located on the lower left corner of the front of the carton. If the logo has an orange or…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1531-2018·2018-05-02

    BD Vacutainer Push Button Blood Collection Set Recalled for Sterility Failure

    Becton Dickinson & Company is recalling BD Vacutainer Push Button Blood Collection Sets because they do not meet the labeled sterility assurance level.

    Product
    BD Vacutainer¿ Push Button Blood Collection Set 0.6 x 19 mm x 305 mm 23G x ¿ x 12 (Catalog no 367342)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1505-2018·2018-05-02

    Stryker T4 Zipper Toga sterile garments recalled for layer separation

    Stryker is recalling T4 Zipper Toga sterile personal protection garments because material layers may separate, creating a risk of exposure to contaminants.

    Product
    T4 Zipper Toga (S/M); Catalog Number: 0400-810-000 Sterile personal protection garment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1471-2018·2018-05-02

    Zimmer Biomet Recalls Pressure Sentinel Guide Wires Due to Sterile Seal Failure

    Zimmer Biomet is recalling 19,483 Pressure Sentinel Intramedullary Reaming System Guide Wires because the sterile packaging seal may fail, potentially compromising sterility.

    Product
    Pressure Sentinel Intramedullary Reaming System Guide Wire Bullet Tip 2.4 mm Diameter; Item Number: 00-2228-024-00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1472-2018·2018-05-02

    Zimmer Biomet Recalls Natural Nail System Guide Wires Due to Sterile Seal Failure

    Zimmer Biomet is recalling 19,483 Natural Nail System Tear Drop Guide Wires because the sterile packaging seal may fail, potentially compromising sterility.

    Product
    Zimmer Natural Nail System Tear Drop Guide Wire 2.4 mm Diameter, 100 cm Length; Diameter; Item Number: 47-2490-097-01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1487-2018·2018-05-02

    Integra LifeSciences Recalls TCC-EZ Total Contact Cast System

    Integra LifeSciences is recalling 250 units of the TCC-EZ Total Contact Cast System because a quarantined lot may produce excessive heat.

    Product
    TCC-EZ, Total Contact Cast System, Model No. TCC2-4051
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1130-2018·2018-05-02

    MMRF Neyyappam Recalled for Undeclared Milk Allergen

    Maharaja Food Importers is recalling frozen MMRF Neyyappam because the label lists ghee but fails to declare milk, a major allergen.

    Product
    MMRF Neyyappam, UPC: 870400000111, Frozen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1129-2018·2018-05-02

    MMRF Kumbiliappam Recalled for Undeclared Milk Allergen

    Maharaja Food Importers is recalling frozen MMRF Kumbiliappam because the label lists ghee but fails to declare milk as an ingredient.

    Product
    MMRF Kumbiliappam, UPC: 87040000104, Frozen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0725-2018·2018-05-02

    Coastal Meds Recalls Methylcobalamin Injectable Due to Particulate Matter

    Coastal Meds, LLC. is recalling 4,524 vials of Methylcobalamin Injectable due to the presence of unknown particulate matter.

    Product
    METHYLCOBALAMIN Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
    Category
    Drug
    Distribution
    Distributed nationwide