Severity 4 of 5

Severe recalls

The hazard poses a serious risk of illness, injury, or structural failure. 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.

15151–15175 of 29202

SevereFDA (Food)·F-0471-2018·2017-12-06
Yorgo's Foods Vegetable Hummus Recalled for Listeria Contamination
Yorgo's Foods is recalling Vegetable Hummus in 8 oz and 5 lb containers due to potential Listeria monocytogenes contamination. The product was distributed in New York and New Jersey.
Product
Yorgo's Foods VEGETABLE HOMMUS NET WT 8 OZ (227g) UPC: 7 56248 10008 7 and Yorgo's Foods VEGETABLE HOMMUS NET WT. 5 LBS 80 OZ(2268g). Product is packaged in a clear plastic container, keep refrigerated.
Category
Food
Distribution
2 states
SevereFDA (Food)·F-0460-2018·2017-12-06
Yorgos Foods Green Olive Hummus Recalled for Listeria Contamination
Yorgos Foods is recalling Green Olive Hummus due to potential Listeria monocytogenes contamination. The product was distributed in New York and New Jersey.
Product
Yorgos FOODS Green Olive Hommus NET WT 8 OZ (227g) UPC: 7 56248 10032 2. Product is packaged in a clear plastic container, keep refrigerated.
Category
Food
Distribution
2 states
SevereNHTSA·17V781000·2017-12-06
Audi Recalls 2012-2014 A6 and A7 Models for Fuel Line Fire Risk
Volkswagen Group of America is recalling 2012-2014 Audi A6 and A7 vehicles because a weakening fuel line compression point can cause leaks and increase fire risk.
Product
AUDI — AUDI A6, A7
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V780000·2017-12-06
Starcraft Bus Prodigy and Quest School Bus Fuel Line Recall
Forest River is recalling 2017 Starcraft Bus Prodigy and Quest school buses because floor screws may damage fuel lines, risking leaks, engine stalls, or fires.
Product
STARCRAFT BUS — STARCRAFT BUS QUEST, PRODIGY
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0466-2018·2017-12-06
Yorgo's Foods Black Bean Salad Recalled for Listeria Contamination
Yorgo Food's Inc. is recalling specific sizes of Black Bean Salad due to potential Listeria monocytogenes contamination. The product was distributed in New York and New Jersey.
Product
Yorgo's Foods BLACK BEAN SALAD NET WT. 5 LBS 80 OZ (2268g) UPC: 7 56248 10069 and Yorgo's Foods BLACK BEAN SALAD NET WT. 12 OZ (340g)UPC: 7 56248 10062 9. Product is packaged in a clear plastic container, keep refrigerated.
Category
Food
Distribution
2 states
SevereFDA (Food)·F-0476-2018·2017-12-06
Yorgo's Foods Tzatziki Recalled for Listeria monocytogenes Contamination
Yorgo Food's Inc. is recalling Tzatziki products in New York and New Jersey due to potential Listeria monocytogenes contamination.
Product
Yorgo's Foods TZATZIKI NET WT 8 OZ (227g) UPC: 7 56248 10053 7 and Yorgo's Foods TZATZIKI NET WT. 5 LBS 80 oz (2268g). Product is packaged in a clear plastic container, keep refrigerated.
Category
Food
Distribution
2 states
SevereFDA (Food)·F-0474-2018·2017-12-06
Yorgo's Foods Recalls Three Bean Salad Due to Listeria Contamination
Yorgo Food's Inc. is recalling specific sizes of Three Bean Salad because the product may be contaminated with Listeria monocytogenes.
Product
Yorgo's Foods THREE BEAN SALAD NET WT. 5 LBS 80 oz (2268g) UPC: 7 56248 10071 1 and Yorgo's THREE BEAN SALAD NET WT. 12 OZ (340g) UPC: 7 56248 10063 6. Product is packaged in a clear plastic container, keep refrigerated.
Category
Food
Distribution
2 states
SevereFDA (Food)·F-0470-2018·2017-12-06
Yorgo's Foods Garlic and Chive Hummus Recalled for Listeria Risk
Yorgo Food's Inc. is recalling Garlic and Chive Hummus due to potential Listeria monocytogenes contamination. The product was distributed in New York and New Jersey.
Product
Yorgo's Foods GARLIC AND CHIVE HOMMUS NET WT 8 OZ (227g) UPC: 7 56248 10034 6. Product is packaged in a clear plastic container, keep refrigerated.
Category
Food
Distribution
2 states
SevereFDA (Food)·F-0465-2018·2017-12-06
Yorgo's Tahini Sauce Recalled for Listeria Contamination Risk
Yorgo Food's Inc. is recalling Tahini Sauce products due to potential Listeria monocytogenes contamination. The affected products were distributed in New York and New Jersey.
Product
Tahini Sauce: TRADER JOE S TAHINI SAUCE NET WT 8 OZ (227g) UPC: 0078 7239; Yorgo's Foods TAHINI SAUCE NET WT. 5 LBS 80 OZ (2268g)Product is packaged in a clear plastic container, keep refrigerated.
Category
Food
Distribution
2 states
SevereFDA (Food)·F-0459-2018·2017-12-06
Yorgo's Foods Garlic Hommus Recalled for Listeria Contamination
Yorgo Food's Inc. is recalling Garlic Hommus products in New York and New Jersey due to potential Listeria monocytogenes contamination.
Product
Yorgos FOODS Garlic Hommus 8 oz. (227g) UPC: 7 56248 10015 5 and 16 oz. (454g) UPC: 7 56248 10014 8. Yorgo's Foods GARLIC HOMMUS NET WT. 5 LBS 80 OZ (2268g) Product is packaged in a clear plastic container, keep refrigerated.
Category
Food
Distribution
2 states
SevereCPSC·18047·2017-12-05
Netgear Recalls Outdoor Camera Power Adapters Due to Fire Hazard
Netgear is recalling VMA4700 power adapters for Arlo outdoor cameras because water leakage can cause short circuits, melting, and fire.
Product
Power adapters for outdoor Arlo cameras
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·17V776000·2017-12-04
Burch Recalls 1984 Evans Cargo Tank Trailers Due to Brake Caliper Bolts
Burch Tank and Truck is recalling 1984 Evans Cargo Tank trailers because improperly torqued brake caliper bolts may allow the caliper to detach, increasing crash risk.
Product
EVANS — EVANS CARGO TANK
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V778000·2017-12-04
Triple E RV Recalls 2016-2018 Wonder Motorhomes for Seat Bolt Issue
Triple E RV is recalling 2016-2018 Wonder motorhomes because improperly tightened passenger seat bolts may fail in a crash, increasing injury risk.
Product
TRIPLE E RV — TRIPLE E RV WONDER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V775000·2017-12-01
Ford Recalls 2018 Expedition Vehicles for Seat Back Bolt Defect
Ford is recalling 2018 Expedition vehicles because second-row outboard seats may have improperly installed bolts or excessive forward adjustment, increasing injury risk in a crash.
Product
FORD — FORD EXPEDITION
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V772000·2017-12-01
MV Agusta Recalls 2017 Brutale 800 Dragster RR for Rear Wheel Spokes
MV Agusta is recalling 45 2017 Brutale 800 Dragster RR motorcycles because rear wheel spokes may loosen, potentially affecting handling and increasing crash risk.
Product
MV AGUSTA — MV AGUSTA BRUTALE 800 DRAGSTER RR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V769000·2017-11-30
Hyundai Recalls 2013-2014 Elantra for Brake Pedal Stopper Pad Defect
Hyundai is recalling 2013-2014 Elantra vehicles because a deteriorating brake pedal stopper pad can cause brake lights to stay on and allow shifting out of park without pressing the brake pedal.
Product
HYUNDAI — HYUNDAI ELANTRA
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0368-2018·2017-11-29
Icybay Brand Frog Legs Recalled for Unapproved Antibiotics
Slade Gorton & Company is recalling Icybay Brand Frog Legs due to the presence of unapproved antibiotics, nitrofurans and chloramphenicol.
Product
Icybay Brand Frog Legs, 4/6 Ct / Lb Farm Raised Trimmed, Frozen. 30 lb. Master Carton (5 lb. inner boxes 6 boxes per master case) UPC Codes: 073129282770
Category
Food
Distribution
11 states
SevereFDA (Devices)·Z-0160-2018·2017-11-29
FDA Recalls Zimmer Biomet ROSA Surgical Devices Due to Sensor Failure
The FDA is recalling 31 Zimmer Biomet ROSA Surgical Devices because a force feedback sensor may fail, causing the operating arm to continue moving instead of stopping.
Product
ROSA Surgical Device 2.5.8, a computer-controlled electromechanical arm to guide standard neurosurgical instruments.
Category
Medical Device
Distribution
5 states
SevereFDA (Devices)·Z-0141-2018·2017-11-29
Exactech Recalls Optetrak Offset Tibial Trays Due to Design Incompatibility
Exactech is recalling 537 Optetrak Offset Tibial Trays and Screws due to a design incompatibility with certain offset spine stiffener screws and constrained condylar tibial inserts.
Product
Optetrak Offset Tibial Tray and Screws, Size 4F/4T, Beta, Ref 208-04-44, Sterile, RX. .
Category
Medical Device
Distribution
11 states
SevereFDA (Devices)·Z-0150-2018·2017-11-29
Exactech Recalls Optetrak Constrained Condylar Offset Screws Due to Design Incompatibility
Exactech is recalling 953 Optetrak Constrained Condylar Offset Screws because they are design-incompatible with certain tibial inserts and trays.
Product
Optetrak Constrained Condylar Offset Screw, Size FF, Ref 208-04-74, Sterile, RX.
Category
Medical Device
Distribution
11 states
SevereFDA (Devices)·Z-0167-2018·2017-11-29
Zimmer Biomet ROSA Brain 3.0.0 Software Recall for Communication Errors
Zimmer Biomet is recalling 18 units of ROSA Brain 3.0.0 software due to communication errors between software components and the controller.
Product
ROSA Brain 3.0.0 Usage: The device is intended for the spatial positioning and orientation of instrument holders or tool guides to be used by neurosurgeons to guide standard neurosurgical instruments (biopsy needle, stimulation or recording electrode, endoscope). The device…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0140-2018·2017-11-29
Exactech Recalls Optetrak Offset Tibial Tray Due to Design Incompatibility
Exactech is recalling 547 Optetrak Offset Tibial Tray and Screws units due to a design incompatibility with certain offset spine stiffener screws and constrained condylar tibial inserts.
Product
Optetrak Offset Tibial Tray and Screws, Size 4F/4T, Alpha, Ref 208-04-43, Sterile, RX.
Category
Medical Device
Distribution
11 states
SevereFDA (Devices)·Z-0132-2018·2017-11-29
Exactech Recalls Optetrak Offset Tibial Trays Due to Design Incompatibility
Exactech is recalling 665 Optetrak Offset Tibial Trays and Screws due to a design incompatibility with certain offset spine stiffener screws and constrained condylar tibial inserts.
Product
Optetrak Offset Tibial Tray and Screws, Size 1F/1T & 2F/1T, Beta, Ref 208-04-22, Sterile, RX.
Category
Medical Device
Distribution
11 states
SevereFDA (Devices)·Z-0135-2018·2017-11-29
Exactech Recalls Optetrak Offset Tibial Tray Due to Design Incompatibility
Exactech, Inc. is recalling 733 Optetrak Offset Tibial Tray and Screws units due to a design incompatibility with certain offset spine stiffener screws and constrained condylar tibial inserts.
Product
Optetrak Offset Tibial Tray and Screws, Size 3F/2T, Alpha, Ref 208-04-31, Sterile, RX.
Category
Medical Device
Distribution
11 states
SevereFDA (Devices)·Z-0137-2018·2017-11-29
Exactech Recalls Optetrak Offset Tibial Tray Due to Design Incompatibility
Exactech is recalling 720 Optetrak Offset Tibial Trays and Screws due to a design incompatibility with certain offset spine stiffener screws and constrained condylar tibial inserts.
Product
Optetrak Offset Tibial Tray and Screws, Size 3F/3T, Beta, Ref 208-04-34, Sterile, RX.
Category
Medical Device
Distribution
11 states