Severity 4 of 5

Severe recalls

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

5126–5150 of 29102

SevereFDA (Devices)·Z-1427-2023·2023-05-17
Blue Rhino G2 Tracheostomy Introducer Sets Recalled for Unsecure Connections
Cook Incorporated is recalling Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Sets due to unsecure connections with 15mm caps and circuit components that may disconnect during medical procedures.
Product
Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Set, Reference Part Numbers C-PTIS-100-HC-G-EU-FLEX7.5 (G57695), C-PTIS-100-HC-G-EU-FLEX8.5 (G57696), C-PTIS-100-HC-G-NA-FLEX7.5 (G57691), C-PTIS-100-HC-G-NA-FLEX8.5 (G57692)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1490-2023·2023-05-17
ANGIOGUARD RX/XP Emboli Capture Guidewire System May Separate During Procedures
ANGIOGUARD RX/XP emboli capture guidewire systems may separate from their delivery sheaths during interventional procedures, potentially causing stroke. Cordis is recalling 56 units distributed worldwide.
Product
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RM
Category
Medical Device
Distribution
0 states
SevereFDA (Food)·F-0834-2023·2023-05-17
Meijer Tomato Caprese Salad Recalled Due to Listeria Risk
Meijer is recalling Fresh From Meijer Tomato Caprese Salad due to potential Listeria monocytogenes contamination. The product was distributed to stores across six states.
Product
Fresh From Meijer Tomato Caprese Salad 6 Oz UPC - 713733246101
Category
Food
Distribution
6 states
SevereFDA (Devices)·Z-1493-2023·2023-05-17
ANGIOGUARD Emboli Capture Guidewire System recalled due to potential device separation
Cordis US Corp's ANGIOGUARD RX/XP Emboli Capture Guidewire System is being recalled by the FDA (Class I) because the delivery system and capture sheath may separate during medical procedures, potentially requiring emergency intervention.
Product
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RE
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1487-2023·2023-05-17
Emboli Capture Guidewire System Separation Hazard Prompts FDA Recall
The ANGIOGUARD RX/XP Emboli Capture Guidewire System may separate from its delivery sheath during medical procedures, potentially causing stroke or requiring emergency surgery. Cordis US Corp is recalling 146 units worldwide.
Product
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RMC
Category
Medical Device
Distribution
0 states
SevereNHTSA·23V344000·2023-05-12
2023 Ford F-250, F-350, F-450 Super Duty Steering Column May Separate
Ford is recalling certain 2023 F-250, F-350, and F-450 Super Duty vehicles due to loose or missing steering column bolts that could cause steering column separation, increasing the risk of crashes due to loss of steering control.
Product
FORD — FORD F-350 SD, F-250 SD, F-450 SD
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V341000·2023-05-12
Forest River Recalls 2022-2023 Rockport Work Trucks for Brake Wiring
Forest River is recalling 2022-2023 Rockport work trucks because the trailer brake controller may be incorrectly wired, which can cause a loss of brake function and increase crash risk.
Product
FOREST RIVER — FOREST RIVER ROCKPORT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V338000·2023-05-11
Jeep Cherokee Recall: Power Liftgate Electrical Short Fire Risk
Chrysler is recalling 2014-2016 Jeep Cherokee vehicles with power liftgates due to an electrical short that may cause a fire. Owners should park outside until repairs are completed.
Product
JEEP — JEEP CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·23755·2023-05-11
Ski-Doo Snowmobiles Recalled for Fire Hazard from Fuel Leaks
BRP U.S. Inc. is recalling about 12,500 Ski-Doo snowmobiles from model years 2021 and 2022 because a fuel injector hose retainer screw can loosen, cause fuel leaks, and pose a fire hazard. Four fires have been reported.
Product
Ski-Doo snowmobiles
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·017-2023·2023-05-11
Eastern Meat Solutions Recalls Raw Boneless Pork Products Imported Without Reinspection
Eastern Meat Solutions is recalling approximately 40,763 pounds of raw, boneless pork products imported from Canada without FSIS import reinspection. No adverse reactions have been reported.
Product
Eastern Meat Solutions, Inc. Recalls Raw, Boneless Pork Products Imported Without Benefit of Import Reinspection
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·23V335000·2023-05-11
Dennis Eagle ProView Recalled for HVAC Electrical Circuit Overheating Risk
Dennis Eagle is recalling 2020-2023 ProView vehicles because the HVAC electrical circuit may overheat, increasing the risk of a fire.
Product
DENNIS EAGLE — DENNIS EAGLE PROVIEW
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V337000·2023-05-11
BMW Recalls 2007-2014 MINI Cooper Models for Fire Risk
BMW is recalling 2007-2014 MINI Cooper models because a short-circuit in the driver's footwell may cause a fire. Owners should contact dealers for inspection and repair.
Product
MINI — MINI COOPER CLUBMAN, COOPER, COOPER S, JCW
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·23201·2023-05-11
Peloton Exercise Bikes Recalled for Seat Post Breakage and Fall Risk
Peloton is recalling approximately 2.2 million Model PL01 exercise bikes because the seat post assembly can break during use, causing users to fall. The company has received 35 reports of seat post breakage, including 13 reports of injuries such as fractured wrists, lacerations, and bruises.
Product
Peloton Bikes Model PL01
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Food)·F-0818-2023·2023-05-10
Tandoori Peanut Spread recalled for undeclared milk allergen
Tandoori Peanut Spread is being recalled due to undeclared milk allergen. The product poses a risk to consumers with milk allergies.
Product
Tandoori Peanut Spread; Net. Wt 11.29 oz PetJar; packed in cases consisting of 12 Jars per case
Category
Food
Distribution
0 states
SevereUSDA FSIS·016-2023·2023-05-10
Mitten Gourmet Recalls Ready-to-Eat Pork Rinds Produced Without Federal Inspection
Mitten Gourmet is recalling approximately 1,137 pounds of ready-to-eat pork rinds because they were produced without the benefit of federal inspection. Consumers are urged to discard or return the products.
Product
Mitten Gourmet, LLC, Recalls Ready-to-Eat Pork Rind Products Produced without Benefit of Inspection
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0572-2023·2023-05-10
NUX Male Enhancement Capsules Recalled for Undeclared Prescription Ingredients
The FDA recalls NUX Male Enhancement capsules distributed nationwide because they contain undeclared sildenafil and tadalafil, making them an unapproved drug. Consumers should not use this product.
Product
NUX Male Enhancement capsule, 1-count blister card, distributed by SX Power CO., Chicago, Il 60612, UPC 6 01577 51236 3.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0571-2023·2023-05-10
Pro Power Knight Plus Capsule Recalled for Undeclared Pharmaceutical Ingredients
Pro Power Knight Plus capsules contain undeclared sildenafil and tadalafil, prescription ingredients not listed on the label. The product was marketed as an unapproved drug and poses safety risks.
Product
Pro Power Knight Plus capsule, 2550mg, 1-count blister card, Distributed by Beyond Health and youth Inc, Seattle, WA 98110, UPC 4 94922 90522 0.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0771-2023·2023-05-10
Scarpetta Pink Pesto Pasta Sauce Recalled for Undeclared Pine Nuts
Scarpetta brand Pink Pesto Pasta Sauce contains undeclared pine nuts. Consumers with tree nut allergies are at risk of allergic reactions.
Product
Scarpetta brand Pink Pesto Pasta Sauce; INGREDIENTS: Tomatoes (tomatoes, tomato juice, citric acid), Cream, Onions, Olive Oil, Basil, Garlic, Salt, Black Pepper, Citric Acid.; CONTAINS: MILK.; BC Gourmet USA, Inc., Lynn, MA;
Category
Food
Distribution
3 states
SevereFDA (Food)·F-0774-2023·2023-05-10
Dark Chocolate Pineapple Bites Recalled Due to Undeclared Milk
Salento Organics has recalled Dark Chocolate Pineapple Bites due to undeclared milk. The affected product contains milk not identified on the label, posing a risk to consumers with milk allergies.
Product
Salento Organics, Dark Chocolate Pineapple Bites, Net WT. 4oz (113G)
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0815-2023·2023-05-10
Tandoori Roasted Chana Recalled Due to Undeclared Milk Allergen
Tandoori Roasted Chana (chickpeas) from Jabsons Foods is recalled because it contains undeclared milk, a major allergen. Consumers with milk allergies should not consume this product.
Product
Tandoori Roasted Chana (Chick Peas); Net. Wt 4.94 oz Laminated Pouches; packed in cases consisting of 24 pouches
Category
Food
Distribution
0 states
SevereFDA (Drugs)·D-0573-2023·2023-05-10
Unapproved Drug Capsule Recalled for Undeclared Sexual Enhancement Ingredients
DYNAMITE SUPER capsule is being recalled nationwide because it was marketed without FDA approval and contains undeclared sildenafil and tadalafil, active ingredients used in sexual enhancement products.
Product
DYNAMITE SUPER capsule, 58,000 MG, 1-count blister card, Made in America, UPC 6 75799 37602 7.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0777-2023·2023-05-10
Dark Chocolate Pitaya Bites Recalled for Undeclared Milk
Salento Organics Dark Chocolate Pitaya Bites are recalled for undeclared milk. The product poses a risk to consumers with milk allergies.
Product
Salento Organics, Dark Chocolate Pitaya Bites, Net WT. 4oz (113G)
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0817-2023·2023-05-10
FDA recalls Tandoori Kaju Cashew Nuts for undeclared milk allergen
Jabsons Foods has voluntarily recalled Tandoori Kaju Cashew Nuts because the product contains undeclared milk, a common allergen. This is a Class I recall affecting consumers with milk allergies.
Product
Tandoori Kaju- Cashew Nuts; Net. Wt 3.53 oz Laminated Pouches; packed in cases consisting of 48 pouches
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0819-2023·2023-05-10
Thai Sweet Chilli Roasted Peanut Recalled for Undeclared Milk
Jabsons Foods is recalling Thai sweet Chilli Roasted Peanut due to undeclared milk. The recall affects 508 cases distributed domestically in the United States.
Product
Thai sweet Chilli Roasted Peanut; Net. Wt 4.94 oz laminated pouches; packed in cases consisting of 24 pouches per case
Category
Food
Distribution
0 states
SevereNHTSA·23V334000·2023-05-10
GM Recalls 2014-2017 SUVs for Driver Air Bag Inflator Defect
General Motors is recalling 2014-2017 Buick Enclave, Chevrolet Traverse, and GMC Acadia vehicles because the driver's air bag inflator may explode during deployment.
Product
BUICK — BUICK, CHEVROLET, GMC ENCLAVE, TRAVERSE, ACADIA
Category
Vehicle
Distribution
Distributed nationwide