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 deaths or serious injuries are reported, 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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All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

24526–24550 of 26084

  • HighFDA (Devices)·Z-2474-2021·2021-09-22

    Philips Allura Xper X-ray imaging system failures at 480V power supply

    Four Philips Allura Xper X-ray imaging systems may fail prematurely when powered at 480V hospital mains, causing coil overheating and reduced imaging performance.

    Product
    The Allura Xper series is intended for use on human patients to perform: "Vascular, cardiovascular and neurovascular imaging applications, including diagnostic, interventional and minimally invasive procedures. This includes, e.g., peripheral, cerebral, thoracic and abdominal a
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2450-2021·2021-09-22

    Diagnostic reagent kits recalled for incorrect chemical composition

    Gibson Bioscience is recalling Potassium Hydroxide 10% diagnostic reagent kits (Lot 21137116, 11 units) manufactured with Hydrogen Peroxide 3% instead of the intended chemical. The wrong solution could cause inaccurate laboratory test results.

    Product
    Potassium Hydroxide 10% (KOH 10%), Cat. No. 300145 Potassium Hydroxide 10% (KOH 10%) is intended for use in the demonstration of yeast and fungal elements in wet clinical preparations. Potassium Hydroxide digests the proteinaceous material in the specimen, leaving the fungal c
    Category
    Medical Device
    Distribution
    7 states
  • HighFDA (Devices)·Z-2451-2021·2021-09-22

    FDA Recalls Luminex Verigene Enteric Pathogen Test Kits for False Positive Results

    Luminex Corporation is recalling 4,579 Verigene EP Amplification Reagent Kit Test units worldwide due to potential for false positive results. Affected kits distributed across the United States, Austria, France, Greece, Japan, and Turkey may produce incorrect test results.

    Product
    Verigene EP Amplification Reagent Kit Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21199·2021-09-22

    Oceanic Adult Dry Top Snorkels Recalled Due to Drowning Hazard

    Huish Outdoors is recalling Oceanic Adult Dry Top Snorkels sold at Costco because the bottom purge valve can leak, allowing unexpected water entry that poses a drowning hazard. Consumers should stop using the snorkels immediately.

    Product
    Oceanic Adult Dry Top Snorkels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2458-2021·2021-09-22

    BD needle-free connector valves may occlude or restrict fluid flow

    BD Burette Gravity Set needle-free connector valves may fail to flush or develop blockages, potentially delaying patient therapy. Lot 21015553 consists of approximately 630 units distributed worldwide.

    Product
    BD BURETTE GRAVITY SET 60 DROP 2 Smartsite VALVES VENTED/NONVENTED, REF: 42163E
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0972-2021·2021-09-22

    Full Tilt Ice Cream All The Chocolate recalled for pasteurization failure

    Full Tilt Ice Cream, LLC is recalling All The Chocolate ice cream in 3-gallon tubs because the ice cream mix did not meet pasteurization specifications, which may pose a food safety risk.

    Product
    All The Chocolate, Full Tilt Ice Cream brand, packaged in 3 gallon tubs. No UPC.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2475-2021·2021-09-22

    Philips Allura Xper Imaging System Overheating and Malfunction Recall

    Philips Allura Xper imaging systems may fail early when supplied with 480V, causing coil overheating and burning smell. When the system fails, X-ray imaging capability is reduced to emergency mode only.

    Product
    The Allura Xper series is intended for use on human patients to perform: "Vascular, cardiovascular and neurovascular imaging applications, including diagnostic, interventional and minimally invasive procedures. This includes, e.g., peripheral, cerebral, thoracic and abdominal
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0981-2021·2021-09-22

    Roasted Red Pepper Flour Wraps Recall Due to Undeclared Wheat

    Tortilleria Sonora is recalling Roasted Red Pepper 12" Supreme Flour Wraps because the product contains undeclared wheat. The case label lists enriched flour but fails to disclose wheat presence, posing a risk to consumers with wheat allergies.

    Product
    Roasted Red Pepper 12" Supreme Flour Wraps, Tortilleria Sonora, Inc.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-2431-2021·2021-09-22

    Cordis Angiographic Catheter Recalled for Marker Band Dislodgement Risk

    Cordis is recalling angiographic catheters that may become entrapped between devices and vessel walls, risking marker band dislodgement during vascular procedures. Approximately 71,330 units were distributed worldwide.

    Product
    Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0974-2021·2021-09-22

    Full Tilt Coffee Oreo Ice Cream Recall for Inadequate Pasteurization

    Full Tilt Ice Cream, LLC is recalling Coffee Oreo ice cream in 3-gallon tubs distributed in Washington because the ice cream mix did not meet pasteurization specifications.

    Product
    Coffee Oreo, Full Tilt Ice Cream brand, packaged in 3 gallon tubs. No UPC.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0983-2021·2021-09-22

    Trader Joe's Raw California Walnut Baking Pieces Mispackaging Recall

    Trader Joe's Raw California Walnut Baking Pieces have been recalled due to mispackaging. Bags labeled as walnut pieces contain a mix of cashews, macadamia nuts, and walnuts.

    Product
    Trader Joe's Nuts Raw California Walnut Baking Pieces NET WT. 16 OZ (1 LB) 454g SKU# 51934-89685 UPC 0051 9342 Contains Walnuts Dist & Sold Exclusive By: Trader Joe's, Monrovia, CA 91016
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-2471-2021·2021-09-22

    Siemens ACUSON Juniper ultrasound system recalled for intermittent power supply failure

    Siemens Medical Solutions USA is recalling 15 ACUSON Juniper Diagnostic Ultrasound Systems worldwide due to intermittent power supply failures that render the devices inoperable. No injuries or illnesses have been reported.

    Product
    ACUSON Juniper Diagnostic Ultrasound System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0968-2021·2021-09-22

    Full Tilt Huckleberry Chip Ice Cream Recall Due to Pasteurization Failure

    Full Tilt Ice Cream is recalling Huckleberry Chip ice cream in 3-gallon tubs distributed in Washington because the ice cream mix did not meet pasteurization specifications, posing a food safety risk.

    Product
    Huckleberry Chip, Full Tilt Ice Cream brand, packaged in 3 gallon tubs. No UPC.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2445-2021·2021-09-22

    Radiation Therapy Software Risk: Data Loss in Treatment Planning

    Siemens radiation therapy planning software may lose data when editing treatment structures. Incomplete structure sets could be sent to the treatment planning system, affecting treatment plan accuracy.

    Product
    syngo.via RT Image Suite with syngo.via VB30, VB40, VB50 and VB60- Intended for Radiation Therapy Treatment Material Number: 10496180
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2468-2021·2021-09-22

    BD Needle-Free Bag Access Valves Recalled for Flow Obstruction

    BD SmartSite needle-free valves may become obstructed, preventing proper fluid flow in medical infusions. The FDA recalls over 295,000 units due to risk of therapy delays.

    Product
    BD SmartSite Bag Access Device Needle-Free Valve, REF: 2300E; BD Bag access Device with 1 Check Valve And Needle Free Valve, REF: 2309E-0006
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2455-2021·2021-09-22

    BD SmartSite Needle-Free Valve Extension Set Recalled for Potential Occlusion

    CareFusion recalls BD SmartSite needle-free valve extension sets due to potential occlusion, flow issues, and difficulty flushing that could delay medical therapy.

    Product
    BD SmartSite 'Y' Extension Set 2 Needle-Free Valves, REF: 20019E7D
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0969-2021·2021-09-22

    Full Tilt Thai Tea Ice Cream Recall for Insufficient Pasteurization

    Full Tilt Ice Cream is recalling Thai Tea ice cream in 16oz pints and 3-gallon tubs because the ice cream mix did not meet pasteurization specifications, creating a risk of harmful bacterial contamination.

    Product
    Thai Tea, Full Tilt Ice Cream brand, packaged in 16oz pre packed pints and 3 gallon tubs. UPC on pint container: 00856962005290.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2457-2021·2021-09-22

    BD Syringe Set Needle-Free Connector Valves May Cause Therapy Delay

    BD Syringe Set needle-free connector valves may experience difficulty flushing, flow issues, or occlusions that could delay patient therapy. About 16,700 units have been distributed worldwide.

    Product
    BD Syringe Set 20 DP MIC TBG 0.2MF CKV Anti-Siphon SmartSite VLV Sensing Disc, REF: 10798696; BD Syringe Set 20 DP MIC TBG CKV Anti-Siphon SmartSite VLV Sensing Disc, REF: 10798703;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0961-2021·2021-09-22

    Marketside Chocolate Candy Cookie Cake Recalled for Undeclared Peanut Allergen

    Jimmy's Cookies, LLC is recalling Marketside Chocolate Candy Cookie Cake (24 oz., Lot# 1133) because the product contains undeclared peanuts, posing a serious risk to consumers with peanut allergies.

    Product
    Marketside Chocolate Candy Cookie Cake, 24 oz. 12 x 12 black tray with clear lid.
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-2456-2021·2021-09-22

    FDA recalls BD burette sets for connector valve occlusion and flow defects

    BD Gravity Burette Sets and Add-On Burette Sets are being recalled due to needle-free connector valve defects that may cause flushing difficulties, flow problems, or complete occlusions, potentially delaying therapy. The recall affects approximately 77,802 units distributed worldwide.

    Product
    BD Gravity Burette Set 60 DROP 1.2 MF 2 SmartSite VALVES BALL VALVE DRIP CHAMBER V/NV, REF: 10037031; BD Gravity Burette Set 20 DROP 1.2 Micron Filter 2 SmartSite VALVES BALL VALVE DRIP CHAMBER V/NV , REF: 10037032; BD GRAVITY BURETTE SET 60 DROP 2 Smartsite VALVES BALL DRIP CHAM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0982-2021·2021-09-22

    Jimbo's Bloody Mary Mix Recalled for Undeclared Soy, Sulfites, Wheat

    Jimbo's Kitchen is recalling Jimbo's Bloody Mary Mix because the product contains soy, sulfites, and wheat that are not declared on the ingredient label, posing a risk to consumers with allergies or sensitivities.

    Product
    Jimbo's BLOODY MARY MIX; 2.5OZ MAKES ABOUT 45 SERVINGS; Ingredients: Horseradish Powder, Parsley, Worcestershire Powder, Cayenne Pepper, Lemon Peel, Black Pepper, Celery Seed Powder, Lemon Juice Crystals, Sea Salt; Hand made in a facility that contains wheat, dairy, eggs and nuts
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-2467-2021·2021-09-22

    BD SmartSite Needle-Free Connector Valves Recalled for Flow and Occlusion Issues

    CAREFUSION is recalling BD SmartSite needle-free connector valves due to difficulty flushing, flow issues, and occlusions that could delay therapy. Approximately 23.8 million units were distributed worldwide.

    Product
    BD SmartSite, REF: 2000E CHINA; BD SmartSite Connector, REF: 2000E-04; BD SmartSite J-LOOP Extension Set One Needle Free Valve, REF: 20021E7D; BD SmartSite Extension Set One Needle Free Valve Slip Luer, REF: 20037E7D; BD SmartSite Extension Set 3 Needle Free Valves, REF: 20038E7D
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2465-2021·2021-09-22

    BD SE Burette Set needle-free connectors recalled for flow obstruction risk

    CareFusion is recalling BD SE Burette Sets with needle-free connector valves that may fail to flush or develop flow obstructions, risking therapy delays. Approximately 56,680 units were distributed worldwide.

    Product
    BD SE Burette Set 20 Drops 2 Injection Ports Vented/NonVented, REF: 72103E-0006
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2444-2021·2021-09-22

    Roche cobas infinity software may release incorrect test results to laboratories

    Roche Diagnostics is recalling cobas infinity central lab software versions 3.01.03–3.02.08 because under certain circumstances, the software may automatically send false test results to laboratory information systems. Correct results remain available on the instrument.

    Product
    cobas infinity central lab running software version 3.01.03 through 3.02.08, Catalog#: 07154003001
    Category
    Medical Device
    Distribution
    Distributed nationwide