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.

Filters

Agency

All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

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

Clear filters

27001–27025 of 39747

  • SevereFDA (Devices)·Z-2326-2015·2015-08-12

    Aesculap S4C Occiput Torque Wrench Recalled Due to Reassembly Defect

    Aesculap is recalling 10 S4C Occiput Torque Wrenches because improper reassembly after reprocessing caused a screw to break during implantation.

    Product
    S4C Occiput Torque Wrench F/Set Screw; used to tighten the S4 Cervical Spinal System clamping screws with a defined torque 2.8 Nm for tightening the clamping screw in the screw head/hook head/occipital plate/transverse connector and other connectors.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2317-2015·2015-08-12

    Cook Inc. Recalls Beacon Tip Torcon NB Advantage Catheters

    Cook Inc. is recalling Beacon Tip Torcon NB Advantage Catheters due to reports of tip splits or separation, which may cause loss of function or complications.

    Product
    Beacon Tip Torcon NB Advantage Catheter. Angiographic catheter. For use in angiographic procedures as a conduit for the delivery of contrast media and can help physicians diagnose occlusion or stenosis. The catheters are designed for percutaneous introduction into the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2324-2015·2015-08-12

    Medtronic Passive Biopsy Needle Kit Recalled for Adhesive Defect

    Medtronic is recalling 1,415 Passive Biopsy Needle Kits because compromised adhesive may cause the sphere assembly to move, leading to inaccurate navigation during brain biopsies.

    Product
    Medtronic Passive Biopsy Needle Kit, Part Number 9733068 - Passive Biopsy Needle Kit. The image guided Passive Biopsy Needle is an accessory instrument with the StealthStation System. The Biopsy Needle is intended to be used for stereotaxy biopsy of brain tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2912-2015·2015-08-12

    Osamu Recalls Raw Frozen Saku Tuna Due to Salmonella Risk

    Osamu Corporation is recalling raw frozen saku tuna products from Indonesia due to potential Salmonella contamination. The recall covers bulk frozen tuna distributed to 15 U.S. states and D.C.

    Product
    Raw Frozen Saku Tuna Product of Indonesia. The bulk frozen tuna products can be identified from the Purchase Order Number (PO#) printed on each product carton box end panel.
    Category
    Food
    Distribution
    15 states
  • SevereFDA (Drugs)·D-1296-2015·2015-08-12

    Apothecary Shoppe Recalls Papaverine and Phentolamine Injection Due to Sterility Concerns

    The Apothecary Shoppe is recalling specific lots of SIU-Papav/Phentol 30/1 mg/mL Injection due to a lack of documentation for environmental monitoring during production.

    Product
    SIU-Papav/Phentol 30/1 mg/mL Injection, Rx Only, 5 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 99999-6830-10
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1295-2015·2015-08-12

    Apothecary Shoppe Recalls Papaverine and Phentolamine Injection Due to Sterility Concerns

    The Apothecary Shoppe LLC is recalling specific vials of Papaverine and Phentolamine Injection due to a lack of documentation confirming proper environmental monitoring during production.

    Product
    SIU-Papav/Phent 24/1 mg/mL Inj., Rx Only, 10 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 13861-1461-57
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-2939-2015·2015-08-12

    Wish-Bone Ranch Dressing Recalled for Undeclared Eggs

    Pinnacle Foods is recalling Wish-Bone Ranch Dressing because it contains undeclared eggs, posing a risk to consumers with egg allergies.

    Product
    Wish-Bone Ranch Dressing Net. Wt. 24 oz. Distributed by Pinnacle Foods Group USA LLC Cherry Hill, NJ 08003-3620 UPC 0-41321-00661-6
    Category
    Food
    Distribution
    30 states
  • SevereFDA (Food)·F-2913-2015·2015-08-12

    Osamu Recalls Raw Frozen Tuna Loin Due to Salmonella Risk

    Osamu Corporation is recalling raw frozen tuna loin products from Indonesia due to potential Salmonella contamination. The recall affects bulk frozen tuna distributed to 15 U.S. states and D.C.

    Product
    Raw Frozen Tuna Loin Product of Indonesia. The bulk frozen tuna products can be identified from the Purchase Order Number (PO#) printed on each product carton box end panel.
    Category
    Food
    Distribution
    15 states
  • SevereFDA (Food)·F-2917-2015·2015-08-12

    La Jalpita Walnut Bolis Recalled for Undeclared Milk

    Paleteria La Jalpita is recalling 90 units of La Jalpita brand walnut bolis in Oregon and Washington due to undeclared milk.

    Product
    Walnut bolis (tube), La Jalpita brand, 3.5 fl. oz. No UPC. This product contains artificial flavoring instead of real walnut.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2264-2015·2015-08-12

    Medtronic Recalls EnVeo R Loading Systems Due to Particulate Presence

    Medtronic is recalling EnVeo R Loading Systems because of the presence of particulate. The recall affects 6,912 units worldwide, including 540 in the US.

    Product
    EnVeo R Loading System, Model No. LS-EnVeoR-23, LS-EnVeoR-2629, LS-EnVeoR-23-C, LS-EnVeoR-2629-C. Cardiovascular valve delivery system for use with the Medtronic CoreValve Evolut R system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2910-2015·2015-08-12

    Osamu Recalls Raw Frozen Ground Tuna Due to Salmonella Risk

    Osamu Corporation is recalling raw frozen ground tuna from Indonesia due to potential Salmonella contamination. The products were distributed to 15 states and DC.

    Product
    Raw Frozen Ground Tuna Product of Indonesia. The bulk frozen tuna products can be identified from the Purchase Order Number (PO#) printed on each product carton box end panel.
    Category
    Food
    Distribution
    15 states
  • SevereFDA (Food)·F-2930-2015·2015-08-12

    Charles Products Recalls Shot Glasses Exceeding Lead and Cadmium Limits

    Charles Products Inc. is recalling specific shot glasses because testing revealed lead and cadmium levels exceeding FDA guidance.

    Product
    Shot glasses with decorative artwork that reads Blue: "Who's Your Candy?!" SKU # 835989 Green: "Eye Candy" SKU # 835990 Red: "Hard on the Outside Sweet on the Inside" SKU # 835986
    Category
    Consumer Product
    Distribution
    2 states
  • SevereFDA (Food)·F-2929-2015·2015-08-12

    Charles Products Recalls Pint Glasses Exceeding Lead and Cadmium Limits

    Charles Products Inc. is recalling pint-sized glasses with decorative artwork because testing revealed lead and cadmium levels exceeding FDA guidance.

    Product
    Pint sized glasses with decorative artwork that reads Blue: "Who's Your Candy?!" SKU # 835992 Green: "Eye Candy" SKU # 835993 Red: "Hard on the Outside Sweet on the Inside" SKU # 835991
    Category
    Consumer Product
    Distribution
    2 states
  • SevereNHTSA·15V508000·2015-08-12

    Jeep Renegade Recall for Radio Software Vulnerability

    Chrysler is recalling 2015 Jeep Renegade vehicles to fix a radio software vulnerability that could allow unauthorized remote control of vehicle systems.

    Product
    JEEP — JEEP RENEGADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V505000·2015-08-11

    Mercedes-Benz Recalls 2015-2016 Models for Engine Compartment Fire Risk

    Mercedes-Benz is recalling specific 2015 and 2016 models because a damaged seal may fall into the engine bay, increasing the risk of a fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E400, CLS550, CLS400, E63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V504000·2015-08-11

    Mitsubishi Fuso Trucks Recalled for Brake Pad Shim Corrosion

    Mitsubishi Fuso is recalling certain FEC52, FEC72, and FEC92 trucks because brake pad shims may rust, increasing stopping distance and crash risk.

    Product
    MITSUBISHI FUSO — MITSUBISHI FUSO FEC52, FEC92, FEC72
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V500000·2015-08-10

    GM Recalls 2010 Chevrolet Cobalt Vehicles for Air Bag Wiring Defect

    General Motors is recalling 2010 Chevrolet Cobalt vehicles because a misrouted wiring harness may disable the driver-side curtain air bag, increasing injury risk in a crash.

    Product
    CHEVROLET — CHEVROLET COBALT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V503000·2015-08-10

    Goshen Coach Recalls 2014-2015 Vans Due to Loose Seat Bolts

    Goshen Coach is recalling 1,494 model year 2014-2015 vans because driver and passenger seat bolts may not be properly tightened, increasing injury risk in a crash.

    Product
    GOSHEN — GOSHEN PACER LS, COMMANDER, CONNECTION, SENTINEL UC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15T016000·2015-08-10

    Michelin Recalls BFGoodrich Tires Due to Sidewall Rupture Risk

    Michelin is recalling specific BFGoodrich tires because a sidewall rupture in the bead area may cause rapid air loss, increasing the risk of a vehicle crash.

    Product
    TIRES:BEAD recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V495000·2015-08-06

    Starcraft RV Recalls Launch Ultra Lite Trailers Due to Furnace Defect

    Starcraft RV is recalling 2015-2016 Launch Ultra Lite trailers because improperly secured furnaces may release hazardous exhaust fumes into the cabin.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT LAUNCH ULTRA LITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V498000·2015-08-06

    LGS Recalls 2015-2016 Look, Pace, and Cargo Express Trailers

    LGS Industries is recalling 3,612 model year 2015-2016 Look, Pace, and Cargo Express trailers because the coupler latch may not fully lock, risking separation from the tow vehicle.

    Product
    LOOK — LOOK, PACE, CARGO EXPRESS CARGO TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·15210·2015-08-06

    Viking Range Recalls Dishwashers Due to Fire Hazard

    Viking Range is expanding a recall for about 17,300 dishwashers manufactured before April 2011 because an electrical component can overheat and cause fires.

    Product
    Dishwashers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V493000·2015-08-05

    Forest River Recalls 2015-2016 XLR Trailers for Electrical Fire Risk

    Forest River is recalling 634 model year 2015-2016 XLR trailers because strained wiring at the external power inlet may loosen and arc, increasing the risk of a vehicle fire.

    Product
    FOREST RIVER — FOREST RIVER XLR
    Category
    Vehicle
    Distribution
    Distributed nationwide