The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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21801–21825 of 90109

  • HighFDA (Drugs)·D-0147-2023·2023-01-25

    Eye drop medication Olopatadine HCl recalled nationwide for manufacturing deviations

    Akorn, Inc. is recalling 31,073 bottles of Olopatadine HCl ophthalmic solution nationwide due to current good manufacturing practice deviations. This voluntary recall was initiated by the manufacturer.

    Product
    Olopatadine HCl Ophthalmic Solution, USP 0.1%, 5 mL per dropper bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-105-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0268-2023·2023-01-25

    Klosterman croissant products recalled for insanitary storage conditions

    Klosterman Baking Company is recalling approximately 109,343 croissant products distributed in Indiana, Ohio, and Tennessee due to insanitary storage conditions. Products were delivered between December 12 and December 16, 2022.

    Product
    Breads: Croissant product 9013 Clear film Croissants 64 2.3 oz.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0285-2023·2023-01-25

    Klosterman Baking Company Sour Dough Bread Recalled for Insanitary Production Conditions

    Klosterman Baking Company is recalling approximately 109,343 units of Sour Dough bread products due to insanitary production conditions. Products were distributed in Indiana, Ohio, and Tennessee.

    Product
    Breads: Sour Dough product 1728 Clear Bag Loaf 1 32 oz. Sour Dough product 1729 Clear Bag Loaf 1 32 oz. Sour Dough product 1979 Clear Bag Loaf 1 24 oz. Sour Dough product 8561 Clear Bag Loaf 1 32 oz. Sour Dough product 8563 Clear Bag Loaf 1 32 oz. Sour Dough product 8566…
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0973-2023·2023-01-25

    Cardinal Health Jackson-Pratt Channel Drain Recalled for Performance Defects

    Cardinal Health is recalling Jackson-Pratt Channel Drains (7mm, REF JP-2210) for performance issues including lack of radiopacity, dull trocars, poor flexibility, and broken tips. Affected units may not function properly.

    Product
    Cardinal Health Jackson-Pratt Channel Drain, 7 mm, REF JP-2210
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0275-2023·2023-01-25

    Klosterman Honey Wheat Breads Recalled for Insanitary Storage Conditions

    Klosterman Baking Company recalls honey wheat breads and rolls from Indiana, Ohio, and Tennessee due to products being held under insanitary conditions. Approximately 109,343 units were distributed between December 12-16, 2022.

    Product
    Breads: Honey wheat product 1318 Clear Bag Loaf 1 32 oz. Honey wheat product 1410 Klosterman Retail UPC # 0005172100366 Loaf 1 12 oz. Honey wheat product 8081 Clear Bag Rolls 12 1.4 oz. Honey wheat product 8543 Clear Bag Loaf 1 32 oz. Honey wheat product 8549 Clear Bag Loaf…
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0988-2023·2023-01-25

    Cardinal Health Jackson-Pratt Channel Drain Recalled for Performance Defects

    Cardinal Health Jackson-Pratt Channel Drains (19 Fr, REF JP-2230) are recalled due to performance issues including lack of radiopacity, dull trocars, reduced flexibility, and broken tips affecting 29,515 units.

    Product
    Cardinal Health Jackson-Pratt Channel Drain, 19 Fr, REF JP-2230
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1002-2023·2023-01-25

    X-ray imaging system footrests may detach from patient tables

    Siemens Luminos X-ray imaging systems may have a footrest that detaches from the patient table during use. The manufacturer is recalling 886 units distributed worldwide.

    Product
    Luminos Agile Max, Luminos dRF Max, and LUMINOS Lotus Max
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0276-2023·2023-01-25

    Klosterman Honey White Bread and Buns Recalled for Insanitary Conditions

    Klosterman Baking Company recalls honey white bread and buns held under insanitary conditions. Affected products were distributed in Indiana, Ohio, and Tennessee between December 12-16.

    Product
    Breads: Honey white product 3136 Clear Bag Buns 60 60 g Honey white product 3140 Klosterman Retail UPC # 0005172100106 Buns 12 60 g
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0306-2023·2023-01-25

    Superior Fresh Mighty Mix salad recall: glass particle contamination

    Superior Fresh LLC is recalling Mighty Mix salad mix (4 oz packages, Best By 1/23) due to potential contamination with small glass particles. No injuries have been reported; consumers should discard the product.

    Product
    Superior Fresh Mighty Mix, Net Wt. 4 oz. (113g). UPC 8 57871-00883 9. Ingredients May Contain Red Leaf, Green Leaf, Green Romaine, Red Romaine, Red Oak Leaf, Green Oak Leaf, Arugula, Mizuna, Pak Choi, Spinach. Keep Refrigerated. Grown for you By: Superior Fresh LLC…
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0270-2023·2023-01-25

    Klosterman English Muffins recalled for insanitary storage conditions

    Klosterman Baking Company is recalling English Muffins that were held under insanitary conditions. The recall affects over 109,000 units distributed to Indiana, Ohio, and Tennessee.

    Product
    Breads: English Muffin product 9525 Clear Bag English Muffins 12 2 oz.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0303-2023·2023-01-25

    Superior Fresh Organic Spring Mix Recalled for Glass Particles

    Superior Fresh Organic Spring Mix Family Pack is being recalled due to potential glass particle contamination. The recall affects 1,516 cases distributed in Indiana, Pennsylvania, Virginia, and Wisconsin.

    Product
    Superior Fresh Organic Spring Mix Family Pack. UPC 8 50038-27430 6. Ingredients May Contain Red Leaf, Green Leaf, Green Romaine, Red Romaine, Red Oak Leaf, Green Oak Leaf. Keep Refrigerated. Grown for you By: Superior Fresh LLC, Hixton, WI 54635
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-0989-2023·2023-01-25

    Cardinal Health Jackson-Pratt Channel Drain recall for performance defects

    Cardinal Health is recalling Jackson-Pratt Channel Drains due to performance defects: dull trocars, broken tips, lack of flexibility, and radiopacity issues. The 8,563 affected units were distributed worldwide.

    Product
    Cardinal Health Jackson-Pratt Channel Drain, 19 Fr, REF JP-2231
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0289-2023·2023-01-25

    Klosterman Baking breads and buns recalled for insanitary storage conditions

    Klosterman Baking Company is recalling approximately 109,343 bread and bun products that were held under insanitary conditions. Products were distributed in Indiana, Ohio, and Tennessee.

    Product
    Breads: Yellow product 1444 Clear Bag Loaf 1 32 oz. Yellow product 1675 Clear Bag Loaf 1 24 oz. Yellow product 3139 Clear Bag Buns 12 60 g Yellow product 3148 Clear Bag Buns 12 60 g Yellow product 3385 Clear Bag Buns 12 85 g Yellow product 3396 Clear Bag Buns 12 85 g…
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0263-2023·2023-01-25

    Pepper Collection 8 Tube Gift Set recalled for mold and ochratoxin contamination

    Something South African LLC recalls Pepper Collection 8 Tube Gift Set due to mold (Aspergillus brasiliensis) and Ochratoxin A contamination. The recall affects 4,200 units distributed nationwide.

    Product
    Pepper Collection 8 Tube Gift Set - a colorful assortment of dried peppers. This product contains peppers in 8 different glass tube and packaged in a printed paperboard sleeve and are visible through a window in the sleeve. Net wt. is 4.87oz/138g. The UPC is 6 009686 793712.…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1000-2023·2023-01-25

    Medical X-ray equipment patient table footrests recalled due to detachment risk

    Siemens recalls four fluoroscopy and radiographic imaging equipment models worldwide because patient table footrests may detach during clinical use, potentially causing patient injury.

    Product
    AXIOM Luminos TF, AXIOM Iconos R100, AXIOM Iconos R200 and AXIOM Luminos dRF
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0983-2023·2023-01-25

    Cardinal Health Jackson-Pratt Channel Drain Recalled for Performance Defects

    Cardinal Health is recalling Jackson-Pratt Channel Drains (19 Fr, REF JP-2225) due to multiple performance issues including lack of radiopacity, dull trocars, reduced flexibility, and broken wound tips. Approximately 4,112 units were distributed worldwide.

    Product
    Cardinal Health Jackson-Pratt Channel Drain, 19 Fr, REF JP-2225
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0997-2023·2023-01-25

    Thoracic Stent-Graft System Recalled Due to Dimensional Defect

    Bolton Medical's RELAY PRO thoracic stent-graft system is being recalled because affected units may be shorter than their packaging indicates. The recall affects 129 units distributed worldwide.

    Product
    RELAY PRO, THORACIC STENT-GRAFT SYSTEM, REF 28-M4-XX-XXX-XXX
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0302-2023·2023-01-25

    Superior Fresh Lettuce Blend Recalled for Small Glass Particles

    Superior Fresh Lettuce Blend products have been recalled due to the presence of small glass particles. Affected products include Spring Mix, Midwest Medley, and Midwest Medley Family Pack distributed in Indiana, Pennsylvania, Virginia, and Wisconsin.

    Product
    Superior Fresh Lettuce Blend Ingredients May Contain Red Leaf, Green Leaf, Green Romaine, Red Romaine, Red Oak Leaf, Green Oak Leaf, Butter lettuce, Arugula, Kale, Spinach, Mustard, Mizuna, Pax Choi. Keep Refrigerated. Packaged under the following Names and sizes: 1.…
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-0981-2023·2023-01-25

    Cardinal Health Jackson-Pratt Channel Drains recalled for multiple performance defects

    Cardinal Health is recalling Jackson-Pratt Channel Drains (10 Fr, REF JP-2221) due to multiple performance issues including broken wound tips, dull trocars, lack of radiopacity, and reduced flexibility affecting 179 units distributed worldwide.

    Product
    Cardinal Health Jackson-Pratt Channel Drain, 10 Fr, REF JP-2221
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0996-2023·2023-01-25

    Vasoshield Syringe Packs Recalled Due to Chipping Ink Risk

    Maquet Cardiovascular is recalling Vasoshield Syringe Packs (Model VH-5001) because ink on the syringe logo may chip, creating a risk of foreign body complications and embolic events. The recall affects 530 units in the United States and 215 units outside the United States.

    Product
    Vasoshield Syringe Packs, Model VH-5001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0166-2023·2023-01-25

    Hand Sanitizer Recalled for Chemical Impurities and Manufacturing Defects

    SIREtizer Hand Sanitizer is recalled for containing acetal and acetaldehyde above allowable limits and manufacturing defects, including one superpotent lot.

    Product
    SIREtizer Hand Sanitizer (Ethyl Alcohol) 80%, packaged in a) 3.38 oz (100 mL), b) 10 oz (295 ml), UPC 8 60003 85882 0, and c) 16.9 oz (500 ml), UPC 8 60003 85880 6 bottles, Southwest Iowa Renewable Energy, 10868 189th Street, Council Bluffs, IA 51503; Bottled by Southwest 6th…
    Category
    Drug
    Distribution
    2 states
  • HighFDA (Devices)·Z-0971-2023·2023-01-25

    Cardinal Health Jackson-Pratt Channel Drains Recalled for Multiple Performance Defects

    Cardinal Health is recalling 3,507 Jackson-Pratt Channel Drains (19 Fr) due to performance defects including lack of radiopacity, dull trocars, lack of flexibility, and broken tips. Drains were distributed worldwide.

    Product
    Cardinal Health Jackson-Pratt Channel Drain, 19 Fr, REF JP-2190
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0156-2023·2023-01-25

    Eye-drop drug recall: Timolol solution due to manufacturing deviations

    Akorn is recalling over 1.3 million bottles of Timolol Maleate eye drops distributed nationwide due to manufacturing process violations. The voluntary recall addresses risks from Current Good Manufacturing Practice deviations.

    Product
    Timolol Maleate Ophthalmic Solution, USP, 0.5%, Packaged in (a) 5 mL dropper bottle, NDC 17478-288-10; (b) 10 mL dropper bottles: NDC 17478-288-11; (c) 15 mL dropper bottles, NDC 17478-288-12; Rx Only, Sterile, Manufactured by: Akorn, Inc., Lake Forest, IL 60045.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V024000·2023-01-23

    Mack Recalls LRBE Electric Trucks Due to Cabin Heater Relay Fire Risk

    Mack Trucks is recalling 2019 and 2021-2023 LRBE electric trucks because a failing cabin heater relay can cause the coolant heater to overheat, increasing the risk of fire.

    Product
    MACK — MACK LRBE (ELECTRIC)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V023000·2023-01-23

    Autocar Recalls Trucks Due to Parking Brake Release Risk

    Autocar is recalling specific trucks because a worn parking brake valve may cause the brake to release unexpectedly, increasing the risk of a crash.

    Product
    AUTOCAR — AUTOCAR XPEDITOR, WX, WXLL, XPERT
    Category
    Vehicle
    Distribution
    Distributed nationwide