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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26176–26200 of 90150

  • HighFDA (Devices)·Z-0813-2022·2022-03-30

    Outset Tablo Hemodialysis Console Recalled for Heat Damage Risk

    Outset Medical is recalling Tablo hemodialysis consoles (models PN-0003000 and PN-0006000) nationwide due to a component that may cause heat-related damage to the device.

    Product
    Outset Tablo Console Model Number: PN-0003000 Model Number: PN-0006000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0820-2022·2022-03-30

    Compella Bariatric Bed System Recall—Power Cord Electrical Shock Risk

    Baxter Healthcare is recalling the Compella Bariatric Bed System due to potential power cord damage that could expose electrical conductors, creating a shock hazard. Approximately 5186 units worldwide are affected.

    Product
    Compella Bariatric Bed System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0901-2022·2022-03-30

    Overnight Oats Recall: Undeclared Almond and Coconut Allergens

    HumbleHungryHappy LLC is recalling Overnight Oats due to undeclared almond and coconut allergens on the label. Consumers with allergies to these ingredients face potential health risks.

    Product
    Overnight Oats, net wt. 9.4 oz. It is packaged in flexible plastic bowl with film lid. Product label is read in parts: "***OVERNIGHT OATS***Ingredients: 1% Greek Yogurt ***Coconut Milk, Orgain Organic Protein, Rolled Oats, Almond, Milk, Honey, Flaxseeds, Coconut***Contains…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0706-2022·2022-03-30

    Norepinephrine Bitartrate Injection Recalled Due to Defective Container

    Athenex Pharma Solutions is recalling Norepinephrine Bitartrate Injection due to defective containers affecting specific lots distributed nationwide.

    Product
    Norepinephrine Bitartrate Injection 4mg per 250 mL in 0.9% Sodium Chloride, 4 mg, 250 mL excel bag, Rx only, Athenex Pharma Solutions, LLC, Clarence, NY, 14031, NDC 76154-474-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0908-2022·2022-03-30

    Snak Yard Dried Plums Recalled for Potential High Lead Content

    Alli & Rose LLC is recalling Snak Yard Dried Plums Saladitos due to potential high lead content. Affected products were distributed in California with best-before dates of February 14, 2023, or April 29, 2023.

    Product
    Snak Yard Dried Plums Saladitos; 12.7 oz. net wt (360g) Item number 1546905 UPC: 8 10019 60082 1 Made in China; Packed in Thailand Distributed by Alli & Rose LLC, 1422 E, ?M?ain St. PMB #210 Lincolnton NC 28092
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0899-2022·2022-03-30

    Damascus Bakery Bantam Classic Bagels Recalled for Undeclared Egg Allergen

    Damascus Bakery is recalling Bantam Classic Bagels due to undeclared egg allergen. Affected product was distributed to SC, PA, MA, MN, NY, and IN.

    Product
    Damascus Bakery, Bantam Classic Bagels, 6/1.3 oz pieces per carton (7.8 oz), Paper Carton .
    Category
    Food
    Distribution
    6 states
  • HighFDA (Drugs)·D-0669-2022·2022-03-30

    FDA Recalls Betamethasone Dipropionate Lotion Due to Manufacturing Deviations

    Teligent Pharma is recalling Betamethasone Dipropionate Lotion due to manufacturing practice deviations and discontinuation of the stability study program. The recall affects 43,218 bottles distributed nationwide.

    Product
    Betamethasone Dipropionate Lotion USP, 0.05%* (Augmented), packaged in a) 30 mL (29 grams) bottles, NDC 52565-023-29; b) 60 mL (58 grams) bottles, NDC 52565-023-59, Rx Only, Teligent Pharma, Inc., Buena, NJ 08310
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0897-2022·2022-03-30

    Flow Alkaline Spring Water Recalled Due to Alleged Adverse Reactions

    Flow Beverages Inc. is recalling Flow Alkaline Spring Water (Organic lemon & ginger, 500 ml) due to four customer complaints of alleged adverse reactions. Affected lots are 2023AUG29 V5, distributed to eleven states.

    Product
    Flow Alkaline Spring Water - Organic lemon & ginger flavored water. 500 ml unit . Tetra Pak paper carton.
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-0734-2022·2022-03-30

    Azurion Medical Imaging System Software Defect Affects Patient Dose Control

    Philips Azurion R2.1 systems have a software defect that causes the Patient Type to change unexpectedly when starting a procedure, potentially affecting dose control settings without user notification.

    Product
    Azurion systems with software release R2.0.x
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0811-2022·2022-03-30

    Biomet Fibula Composite Locking Plate Recall Due to Sterile Barrier Packaging Defect

    Biomet is recalling TRAUMA A.L.P.S. fibula composite locking plates due to packaging that may not maintain sterile barrier integrity, posing a risk of infection if used.

    Product
    BIOMET TRAUMA A.L.P.S. FIBULA COMPOSITE LOCKING PLATE 8 HOLE, Item # 856204008. Devices are packaged in a vacuum sealed nylon pouch, which is placed in a carton with the appropriate IFU and patient record labels. Identifying labels on the pouch and the carton.
    Category
    Medical Device
    Distribution
    28 states
  • HighFDA (Devices)·Z-0810-2022·2022-03-30

    BIOMET Trauma DVR CROSSLOCK implants recalled for packaging integrity

    BIOMET Trauma DVR CROSSLOCK surgical implant plates may have packaging that does not maintain sterile barrier integrity, posing a risk of infection.

    Product
    BIOMET Trauma, [Item # 13182-22-26, DVR CROSSLOCK EXTRA LONG PLATE LEFT], [Item # 1318-12-126, DVR CROSSLOCK EXTRA LONG PLATE RIGHT], [Item # 1318-12-176, DVR CROSSLOCK EXTRA EXTRA LONG PLATE RIGHT]. Devices are packaged in a vacuum sealed nylon pouch, which is placed in a…
    Category
    Medical Device
    Distribution
    28 states
  • HighFDA (Drugs)·D-0681-2022·2022-03-30

    Diflorasone Diacetate Ointment recalled due to discontinued stability studies

    Teligent Pharma is recalling all unexpired Diflorasone Diacetate Ointment 0.05% due to cGMP deviations. The company discontinued its stability study program, preventing verification that the product maintains safety and effectiveness throughout shelf life.

    Product
    Diflorasone Diacetate Ointment USP, 0.05%, Net Wt 60 g tubes, Rx only, Manufactured for: SOLA Pharmaceuticals, LLC Baton Rouge, LA 70809, NDC 70512-031-60.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0812-2022·2022-03-30

    Biomet Trauma Surgical Instruments Recalled Due to Packaging Defect

    Biomet is recalling TRAUMA Drill Bits, Taps, and Guide Pins due to packaging that may not seal properly, potentially compromising sterile barrier integrity and posing a risk of surgical site infection.

    Product
    BIOMET TRAUMA Drill Bit, Tap, Guide Pin: [DVR Drill Bit, Item # 212000022, DVR 2.2MM DRILL BIT], [ALPS Drill Bit, Item # 214227160, 2.7X160MM CALIBRATED DRILL], [ALPS Drill Bit, Item # 824273100, 4.5X150MM DRILL], [ALPS Drill Bit, Item # 829029170, 2.5X140MM DRILL], [ALPS Drill…
    Category
    Medical Device
    Distribution
    28 states
  • HighFDA (Food)·F-0906-2022·2022-03-30

    Thai Noodle Salad Kits recalled for potential foreign material contamination

    Pacific Coast Fruit Company is recalling Kit Thai Noodle Salad FM due to potential foreign material in an ingredient. The product was distributed to retailers in Alaska, Idaho, Oregon, and Washington.

    Product
    Kit Thai Noodle Salad FM; Net weight 6.75 lbs. UPC 0-20728-72698-0. Product is RTE, refrigerated, ready to mix by the retailer for sale at the retail store. Product comes in a kit that contains Thai Noodle Salad Base (recalled by Fresh Creative Foods; RES 89741)…
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-0809-2022·2022-03-30

    Biomet Surgical Implant Reamer Recall: Packaging Sterile Barrier Risk

    Biomet is recalling surgical implant reamers due to packaging that may lose sterile barrier integrity, risking post-surgical infection.

    Product
    BIOMET Sports Medicine JUGGERLOC SLOTTED REAMER: [Item # 110010371, 6MM], [Item #110010372, 7MM], [Item # 110010373, 8MM], [Item #110018275, 5MM]. Devices are packaged in a vacuum sealed nylon pouch, which is placed in a carton with the appropriate IFU and patient record labels.…
    Category
    Medical Device
    Distribution
    28 states
  • SevereNHTSA·22E027000·2022-03-29

    Meritor 180 Series Drive Pinions Recalled for Fracture Risk

    Meritor is recalling 180 Series Drive Pinions because they may fracture. A fractured pinion could engage the parking brake without warning, increasing crash risk.

    Product
    POWER TRAIN:AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V202000·2022-03-29

    2022 Kia Sorento Oil Supply Pipe May Crack, Creating Fire Risk

    Kia is recalling certain 2022 Sorento vehicles because the turbocharger oil supply pipe may crack, causing an oil leak that could increase the risk of engine fire.

    Product
    KIA — KIA SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V203000·2022-03-29

    Travel trailers with defective power inlet bolts risk fire

    Grand Design is recalling certain 2022 Reflection and Transcend travel trailers with 50-amp shore power inlets. The power inlet lug bolts may be too hard to tighten properly, creating loose electrical connections that can cause fire.

    Product
    GRAND DESIGN — GRAND DESIGN REFLECTION, TRANSCEND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V198000·2022-03-28

    Bugatti Recalls One 2018 Chiron for Loose Front Frame Support Screw

    Bugatti is recalling one 2018 Chiron vehicle because a screw fastening the front frame support may be loose, potentially reducing structural protection in a crash.

    Product
    BUGATTI — BUGATTI CHIRON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V195000·2022-03-28

    2022 Keystone Travel Trailers Recalled for Improper Hitch Welds

    Keystone is recalling certain 2022 Bullet, Outback, and Passport travel trailers due to improper welds on the coupler hitch. The defect can cause the trailer to separate from the tow vehicle, increasing crash and injury risk.

    Product
    KEYSTONE — KEYSTONE OUTBACK, BULLET, PASSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V194000·2022-03-28

    Mercedes-Benz Recalls 2022 S-Class Vehicles for Rear Axle Weld Defect

    Mercedes-Benz is recalling 2022 S 500 and S 580 vehicles because a rear axle weld may be defective, posing a risk of loss of vehicle control.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ S 500 4MATIC, S 580 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V152000·2022-03-28

    Certain Volkswagen Atlas vehicles recalled for airbag deployment delay

    Volkswagen is recalling certain Atlas and Atlas Cross Sport vehicles because corroded electrical contacts in the front door wiring harness may delay airbag deployment during side impacts, increasing the risk of injury.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS CROSS SPORT, ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide