The Recall Desk

State

Alabama product recalls

72,992 recalls have nationwide distribution and so reach Alabama. 6,341 additional recalls listed Alabama specifically in their distribution scope.

What the numbers show

Total
6,341
Critical
1,121
Severe
1,337
Most recent
2026-09-02

Of the 6,341 recalls naming Alabama we have scored against our rubric, 1,121 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,337 (21%) are Severe.

Which agencies issued them

These figures cover only the 6,341 recalls whose distribution notice names Alabama specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7576–7600 of 79333

  • CriticalFDA (Devices)·Z-1289-2025·2025-03-19

    Portex Endotracheal Tubes may deliver inadequate ventilation due to smaller diameter

    Portex Endotracheal Tubes from Smiths Medical ASD, Inc. may have a smaller diameter than expected, potentially causing inadequate ventilation and patient hypoxia.

    Product
    Portex Endotracheal Tube, Item Codes 100/105/025 100/105/030 100/105/035 100/111/020 100/111/025 100/111/030 100/111/035 100/111/035 100/126/025 100/126/030 100/126/035 100/127/025 100/127/030 100/127/035 100/141/025 100/141/030 100/141/035
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0609-2025·2025-03-19

    Aleppo Tahini Sesame Paste recalled due to Salmonella contamination

    Turkana Food Inc. is recalling Aleppo Tahini Sesame Paste because the product tested positive for Salmonella. The recalled product was distributed to 23 states.

    Product
    Aleppo Tahini Sesame Paste, 32oz, Plastic jar, 1lb (16oz), 12 per case
    Category
    Food
    Distribution
    23 states
  • CriticalFDA (Food)·F-0633-2025·2025-03-19

    Ulker Biskrem Cocoa Biscuits Recalled for Undeclared Wheat and Egg

    ZB Importing LLC recalls Ulker Biskrem Cocoa Biscuits due to undeclared wheat and egg. Consumers with these allergies should not consume the product.

    Product
    Ulker Biskrem Cocoa Biscuit, item 8836, 10.6oz foil pack, 8 per case, UPC 8690504114628
    Category
    Food
    Distribution
    36 states
  • SevereFDA (Food)·F-0631-2025·2025-03-19

    Ulker Rulokat hazelnut wafers recalled nationwide for undeclared egg allergen

    Ulker Rulokat Hazelnut Wafers are being recalled due to undeclared egg. The product was distributed to retail stores across Canada and 35 US states.

    Product
    Ulker Rulokat Hazelnut Wafers, item 3865, 6oz plastic cylinder, 6 per case, UPC 8690766086473
    Category
    Food
    Distribution
    36 states
  • SevereNHTSA·25V173000·2025-03-19

    Nissan and INFINITI front brake calipers may break losing braking

    Nissan is recalling certain 2025 Murano, Pathfinder and INFINITI QX60 vehicles because one or both front brake caliper assemblies may have reduced strength and could break, failing FMVSS 135.

    Product
    INFINITI — INFINITI, NISSAN QX60, PATHFINDER, MURANO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E020000·2025-03-19

    ZF Recalls Lemförder and TRW Track Control Arms for Subframe Cracking Risk

    ZF North America is recalling specific Lemförder and TRW track control arms because a short bushing sleeve may crack the subframe, potentially causing loss of vehicle control.

    Product
    SUSPENSION:FRONT:CONTROL ARM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0272-2025·2025-03-19

    Injectable Phenylephrine Solution Recalled Due to Particulate Matter Contamination

    The FDA is recalling phenylephrine injection solution due to particulate matter contamination. Three lot numbers distributed nationwide are affected.

    Product
    PHENYLephrine added to 0.9% sodium chloride, 40 mg/250 mL* (160 mcg/mL), Rx Only, CAPS, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, 855-275-2270, NDC 71285-6092-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0268-2025·2025-03-19

    Potassium Chloride Injection Strength Mislabeled on Packaging Overwrap

    ICU Medical recalls Potassium Chloride Injection (lot 1023172) whose overwrap labeled as 10 mEq may contain 20 mEq containers, creating overdose risk. Product distributed nationwide.

    Product
    POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1306-2025·2025-03-19

    Aortic Root Cannula Recall for Loose Male Luer Component

    Medtronic is recalling 316,205 aortic root cannulas due to unexpected loose material in the male luer connector. If not identified before use, this defect could cause stroke; if identified, it may delay surgery.

    Product
    Aortic Root Cannula: 1. DLP Aortic Root Cannula A. CANNULA 11012 AR FLOWGUARD 12GA, model no 11012 B. CANNULA 11014 AR FLOWGUARD 14GA, model no. 11014 2. MiAR Cannula: A. CANNULA 11012L AR FLOWGUARD LONG 12GA, model no 11012L B. CANNULA 11014L AR FLOWGUARD 14FR LONG, m
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0259-2025·2025-03-19

    ChloraPrep One-Step Topical Drug Recalled for Fungal Contamination

    CareFusion 213, LLC is recalling ChloraPrep One-Step, a preoperative skin preparation drug, due to non-sterility from a package lidding breach allowing fungal contamination. The recall affects 205,440 applicators distributed nationwide and in Canada.

    Product
    CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0267-2025·2025-03-19

    Potassium Chloride Injection Recalled: Overwrap Labeling Shows Incorrect Strength

    ICU Medical recalls Potassium Chloride 20 mEq IV injection due to mislabeled overwrap showing 10 mEq instead of the correct strength. The correct dose is printed on the actual container.

    Product
    POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1327-2025·2025-03-19

    Blood Pump Recalled for Potential Fluid Leakage During Clinical Use

    Spectrum Medical is recalling Quantum Perfusion blood pumps due to potential fluid leakage during priming or clinical use. The issue affects approximately 1,487 units distributed nationwide.

    Product
    Brand Name: Quantum Perfusion Centrifugal Blood Pump CP22 with Integrated Sensors Product Name: Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type Model/Catalog Number: CP22V-VT Software Version: N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1329-2025·2025-03-19

    Z1 Femoral Hip System Recalled Over Stem Inserter Design Issue

    Zimmer, Inc. is recalling 35 units of the Z1 Femoral Hip System due to a potential design issue with the Z1 Offset Stem Inserter that could cause fracturing of the distal tip.

    Product
    Z1 Femoral Hip System, Product Number 611777612
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1317-2025·2025-03-19

    ZOLL Powerheart G5 AED May Fail Self-Test After Environmental Exposure

    ZOLL Powerheart G5 AED devices may fail their self-test if exposed to extreme temperatures or humidity. Approximately 56,981 units are being recalled nationwide and internationally.

    Product
    Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-80A, (2) G5A-80A-TSO. Software Version: NA Product Description: The Powerheart G5 automated external defibrillator (AED) is designed for treating life-threatening heart beat irregularities, such as
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0611-2025·2025-03-19

    Genova Yellowfin Tuna Cans Recalled for Botulism Risk

    Genova branded Yellowfin Tuna cans are being recalled because the easy-pull lid was not properly secured, which may cause Clostridium botulinum contamination. The recall affects 14,147 cases distributed nationwide with best-by dates from December 2027 through January 2028.

    Product
    Genova branded Yellowfin Tuna; Genova; In Olive Oil; Wild Caught; NET WT. 5 OZ (142g) RD WT. 4 OZ (113g); Distributed by Tri-Union Seafoods, LLC.; El Sugundo, CA 90245 U.S.A. UPC# 48000 73265 UPC# 48000 13265 UPC# 48000 63267 Product is packaged in several different configurat
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0632-2025·2025-03-19

    Ulker Dankek Roll Cake Strawberry recalled due to undeclared milk allergen

    ZB Importing LLC is recalling Ulker Dankek Roll Cake Strawberry because milk is not declared on the label. Products were distributed in multiple US states and Ontario, Canada.

    Product
    Ulker Dankek Roll Cake Strawberry , item 8298, 8.3oz foil pack, 8 per case, UPC 8690504066828
    Category
    Food
    Distribution
    36 states
  • HighFDA (Devices)·Z-1320-2025·2025-03-19

    ZOLL Powerheart G5 AED may fail self-test in extreme temperatures or humidity

    ZOLL is recalling 73 Powerheart G5 AED units that may fail their internal self-test when exposed to extreme temperatures or humidity. Affected devices could be unreliable in emergencies.

    Product
    Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5S-01C, (2) G5S-02C, (3) G5S-10C, (4) G5S-11C; Software Version: NA Product Description: The Powerheart G5 automated external defibrillator (AED) is designed for treating life-threatening heart beat i
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1321-2025·2025-03-19

    ZOLL Powerheart G5 AED devices may fail self-test in extreme environments

    ZOLL is recalling Powerheart G5 AED devices that may fail their self-test when exposed to extreme temperature or humidity, potentially affecting proper device operation.

    Product
    Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: G5S-80C; Software Version: NA Product Description: The Powerheart G5 automated external defibrillator (AED) is designed for treating life-threatening heart beat irregularities, such as ventricular fibrilla
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0619-2025·2025-03-19

    Van Camp's Canned Tuna Recalled for Potential Botulism Risk from Faulty Lids

    Chicken of the Sea is recalling 14,147 cases of Van Camp's Solid Light Yellowfin Tuna due to improperly secured easy-pull lids that may allow Clostridium botulinum contamination. No illnesses have been reported.

    Product
    Van Camp's branded Solid Light Yellowfin in Vegetable oil; NET WT. 5 OZ (142g) DR WT. 4 OZ (113g); Distributed by: Chicken of The Sea Intl.; El Segundo, CA 90245 U.S.A. UPC# 48000 25015 UPC# 48000 75015
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0618-2025·2025-03-19

    Trader Joe's Solid White Albacore Tuna Recalled for Botulism Risk

    Trader Joe's branded Solid White Albacore Tuna is being recalled because the easy-pull lids were not properly secured, potentially allowing Clostridium botulinum contamination. Approximately 14,147 cases were distributed nationwide.

    Product
    Trader Joe's branded Solid White Albacore Tuna in water, Low sodium; NET WT. 5 OZ (142g) DR WT. 4 OZ (113g); Dist & Sold Exclusively By: Trader Joe's, Monrovia, CA 91816; UPC# 95836
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0273-2025·2025-03-19

    Acne treatment gel recalled for benzene contamination nationwide

    Zapzyt Acne Treatment Gel (10% benzoyl peroxide) distributed nationwide is being recalled due to contamination with benzene. Consumers should stop using affected lots immediately.

    Product
    ZAPZYT ACNE TREATMENT GEL — ZAPZYT ACNE TREATMENT GEL (BENZOYL PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1322-2025·2025-03-19

    ZOLL Powerheart G5 AED Self-Test May Fail Under Extreme Environmental Conditions

    ZOLL is recalling certain Powerheart G5 AED units that may fail their self-test when exposed to extreme temperatures or humidity. The affected devices could fail to function properly in emergencies.

    Product
    Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5S-00A-TSO, (2) G5S-01A, (3) G5S-02A, (4) G5S-05A, (5) G5S-08A, (6) G5S-10A, (7) G5S-11A, (8) G5S-80A-TSO, (9) G5S-80-L (10) G5S-90A; Software Version: NA Product Description: The Powerheart G5 automa
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1308-2025·2025-03-19

    Hemostatic Forceps Recalled Due to Clamp Breakage in Surgical Use

    Aesculap Inc is recalling 19,979 hemostatic forceps across 18 models because clamps can break when instruments are used outside of design specifications.

    Product
    Numerous models of nonsterile hemostatic forceps: (1) REF BJ500R, Phaneuf Hysterectomy Forceps STR 210MM; (2) REF BJ501R, Phaneuf Hysterectomy Forceps ANG 205MM; (3) REF BJ511R, Holzbach Hyst Forceps CVD245MM; (4) REF BJ520R, Heaney Hyst Forceps Grooved 205MM; (5) REF BJ52
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0634-2025·2025-03-19

    Ulker Dankek Roll Cake Chocolate recalled due to undeclared egg allergen

    Ulker Dankek Roll Cake Chocolate is being recalled because egg is not listed in the Contains statement on the product label. Consumers with egg allergies may be at risk.

    Product
    Ulker Dankek Roll Cake Chocolate, item 9584, 3oz foil pack, 8 per case, UPC 8690504067979
    Category
    Food
    Distribution
    36 states