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.

Filters

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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

10076–10100 of 36631

  • SevereFDA (Devices)·Z-0925-2021·2021-02-10

    Hill-Rom Liko Multirall 200 Overhead Lifts Recalled for Detachment Risk

    Hill-Rom is recalling Liko Multirall 200 overhead lifts because a strap lock may not fully engage, causing the lift to detach from the rail and potentially drop the patient.

    Product
    Liko Multirall 200 overhead lift- overhead lift is a general-purpose lift with the intended use in healthcare, intensive care and rehabilitation. Affected devices: Liko Multirall 200 (product number 3130001) Universal SlingBar 450 R2R (product number 3156095) Universal Sling
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V060000·2021-02-08

    BMW Recalls Motorcycles for Fuel Pump Leak Fire Risk

    BMW is recalling 2011-2014 motorcycles because the fuel pump may crack and leak fuel, creating a fire risk.

    Product
    BMW — BMW K 1600 GT, R 1200 GS, K 1600 GTL, S 1000 RR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·21V053000·2021-02-05

    GM Recalls 2009-2013 Trucks and SUVs for Airbag Inflator Defect

    General Motors is recalling specific 2009-2013 Chevrolet, GMC, and Cadillac vehicles because the front passenger airbag inflator may explode, sending metal fragments into the cabin.

    Product
    CHEVROLET — CHEVROLET, GMC, CADILLAC TAHOE, YUKON XL, SIERRA 1500, ESCALADE ESV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·21V050000·2021-02-05

    GM Recalls Trucks and SUVs for Airbag Inflator Explosion Risk

    General Motors is recalling specific 2007-2011 trucks and SUVs because the front passenger airbag inflators may explode due to humidity, posing a risk of serious injury or death.

    Product
    GMC — GMC, CHEVROLET, CADILLAC SIERRA 3500, YUKON, TAHOE, YUKON XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·21V051000·2021-02-05

    GM Recalls 2012 Trucks and SUVs for Airbag Inflator Defect

    General Motors is recalling 2012 Chevrolet, GMC, and Cadillac vehicles because the front passenger airbag inflators may explode, posing a risk of serious injury or death.

    Product
    CHEVROLET — CHEVROLET, GMC, CADILLAC SILVERADO 1500, SILVERADO 3500, YUKON, ESCALADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V052000·2021-02-05

    GM Recalls 2007-2009 Trucks and SUVs for Airbag Inflator Defect

    General Motors is recalling specific 2007-2009 Chevrolet, Cadillac, and GMC vehicles because the front passenger airbag inflators may explode, posing a risk of serious injury or death.

    Product
    CHEVROLET — CHEVROLET, CADILLAC, GMC SUBURBAN, ESCALADE ESV, ESCALADE EXT, AVALANCHE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V057000·2021-02-05

    Mercedes-Benz Recalls GLE and GLS Models for Dashboard Defect

    Mercedes-Benz is recalling 2020-2021 GLE and GLS models because the dashboard may not be properly secured, which could impair airbag inflation in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350, GLE 450, GLS 450, AMG GLE53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V054000·2021-02-05

    GM Recalls 2010-2014 Trucks and SUVs for Airbag Inflator Defect

    General Motors is recalling specific 2010-2014 Cadillac, Chevrolet, and GMC vehicles because the front passenger airbag inflators may explode due to propellant degradation.

    Product
    CADILLAC — CADILLAC, CHEVROLET, GMC ESCALADE EXT, SUBURBAN, TAHOE, SIERRA 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·004-2021·2021-02-05

    Food Evolution Recalls Ready-to-Eat Dip and Salad Products Containing Meat

    Food Evolution is recalling approximately 6,806 pounds of ready-to-eat dip and salad products containing meat because they were produced without federal inspection.

    Product
    Food Evolution — Food Evolution Recalls Ready-to-Eat Dip and Salad Products Containing Meat Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·21V049000·2021-02-04

    Jayco Eagle Fifth Wheel Recall for Incorrect Spring Hanger

    Jayco is recalling 2021 Eagle fifth wheel vehicles equipped with incorrect spring hangers that reduce tire clearance, increasing the risk of tire blowouts.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0221-2021·2021-02-03

    Weis Markets Recalls Nelsons Graham Slam Ice Cream Due to Metal Risk

    Weis Markets is recalling Nelsons Graham Slam bulk ice cream because it may contain metal foreign objects. The product was distributed to retail locations in seven states.

    Product
    Nelsons Graham Slam Bulk. Packaged in a 3 gallon paper drum.
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-0224-2021·2021-02-03

    Port City Bakery Recalls Frozen Pizza Crusts for Glass Contamination

    Port City Bakery is recalling specific lots of Ultimo! ParBaked Raised Edge Pizza Crusts because they may contain glass.

    Product
    Ultimo! ParBaked Raised Edge Pizza Crust packaged in the following sizes: 1. 16" Reorder # 545145, 12 - 18 oz Crusts. Net Wt 13.5 lb. (6.12kg) UPC 00806795511451. 2. 14" Reorder #545147, 10 - 15 oz. Crusts. Net Wt. 9.375 lb. (4.25 kg) UPC 00806795511468. Distribut
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-0921-2021·2021-02-03

    OMNIlife Science Recalls SERF Novae Dual Mobility Cup Inserts

    OMNIlife Science Inc. is recalling 3 units of SERF Novae Dual Mobility Cup Inserts due to high oxidation levels that may increase wear rates and require revision surgery.

    Product
    SERF Novae Dual Mobility Cup Insert 47/28- ApeX-LNK Poly Liner. Intended for use with the Apex Modular Acetabular Cup for total hip replacement procedures. Product Code: H6-24728
    Category
    Medical Device
    Distribution
    5 states
  • SevereFDA (Devices)·Z-0922-2021·2021-02-03

    OMNIlife Recalls SERF Novae Dual Mobility Cup Inserts Due to Oxidation

    OMNIlife science Inc. is recalling 2 units of SERF Novae Dual Mobility Cup Inserts because they have higher than acceptable oxidation limits, which may increase wear rates and require revision surgery.

    Product
    SERF Novae Dual Mobility Cup Insert 49/28-ApeX-LNK Poly Liner. Intended for use with the Apex Modular Acetabular Cup for total hip replacement procedures. Product Code: H6-24928
    Category
    Medical Device
    Distribution
    5 states
  • SevereFDA (Food)·F-0220-2021·2021-02-03

    Weis Markets Recalls Klein's Cookies and Cream Ice Cream for Metal

    Weis Markets is recalling 665 containers of Klein's Cookies and Cream ice cream because the product may contain metal foreign objects.

    Product
    Klein s Cookies and Cream Bulk Packaged in a 3 gallon paper drum.
    Category
    Food
    Distribution
    7 states
  • SevereNHTSA·21V046000·2021-02-03

    BMW Recalls 2020-2021 Models for Driveshaft Breakage Risk

    BMW is recalling specific 2020-2021 530i, 540i, and 740Li vehicles because output shafts may break due to a manufacturing error, potentially causing loss of drive power or rollaway.

    Product
    BMW — BMW 530I, 540I, 740LI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0239-2021·2021-02-03

    IMC Wash-Free Hand Sanitizer Recalled for Methanol Contamination

    Shane Erickson Inc is recalling IMC Wash-Free Hand Sanitizer because it was manufactured at a facility that produced subpotent product containing methanol.

    Product
    IMC Wash-Free Hand Sanitizer, (ethyl alcohol), 75%, 1.7 fl. oz. (50 ml) bottles, Distributed by IMC 4284 Shoreline Dr, Spring Park, MN 55384, Made in China, ALSO distributed with Custom front labels as follows a) Sadie G. Mays Health & Rehabilitation Center, b) Pacers logo, c) no
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0926-2021·2021-02-03

    Medtronic COBALT HF QUAD CRT-D MRI SureScan Recall for Potential Loss of Function

    Medtronic is recalling two specific COBALT HF QUAD CRT-D MRI SureScan devices due to a rare component failure mechanism that could cause loss of function.

    Product
    Medtronic COBALT HF QUAD CRT-D MRI SureScan, Model Number DTPB2QQ, MR Conditional implantable cardioverter defibrillator with cardiac resynchronization therapy, SureScan technology, and Bluetooth wireless telemetry (DDE-DDDR)
    Category
    Medical Device
    Distribution
    3 states
  • SevereFDA (Devices)·Z-0612-2020·2021-02-03

    Enztec Femoral Impactor Recall Due to Arm Fracture Risk

    Enztec Limited is recalling 312 femoral impactors used with the DJO EMPOWR 3D KNEE system because the arm may fracture during use, potentially causing surgical delays or inflammatory responses.

    Product
    REF 800-05-035, ENZTEC FEMORAL IMPACTOR - DJO, (01) 09421028110624 (10) 999999, To be used only with DJO EMPOWR 3D KNEE
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0240-2021·2021-02-03

    IMC Wash-Free Hand Sanitizer Recalled for Methanol Contamination

    Shane Erickson Inc is recalling IMC Wash-Free Hand Sanitizer because it was manufactured at a facility that produced subpotent products containing methanol.

    Product
    IMC Wash-Free Hand Sanitizer, (ethyl alcohol), 75%, 3.4 fl. oz. (100 ml), Made in China, Distributed by IMC 4284 Shoreline Dr, Spring Park, MN 55384. Labeled as a) SAFE-GUARD Products International, b) Safe-WAY JEVCO Wash-Free Hand Sanitizer, c) TRACTION CAPITAL, d) United State
    Category
    Drug
    Distribution
    Distributed nationwide