State

Guam product recalls

72,913 recalls have nationwide distribution and so reach Guam. 385 additional recalls listed Guam specifically in their distribution scope.

What the numbers show

Total: 385
Critical: 14
Severe: 37
Most recent: 2026-01-28

Of the 385 recalls naming Guam we have scored against our rubric, 14 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 37 (10%) are Severe.

Which agencies issued them

These figures cover only the 385 recalls whose distribution notice names Guam specifically. The 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1576–1600 of 73298

ModerateFDA (Devices)·Z-2268-2026·2026-06-10
B. Braun kits contain Mastisol adhesive with potentially cracking tubing
B. Braun CESK Riverside Health System kits are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack, rendering the product unusable.
Product
Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK RIVERSIDE HEALTH SYSTEM Model/Catalog Number: 552126 Software Version: N/A Product Description: CESK RIVERSIDE HEALTH SYSTEM Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·H-1039-2026·2026-06-10
Albertsons parmesan crusted tilapia omits tilapia from contains statement
Albertsons store-made Parmesan Crusted Tilapia is being recalled because the contains statement does not declare tilapia. 15 units are affected.
Product
UPC 21234900000 TILAPIA PARMESAN CRUSTED SS COLD This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·H-1051-2026·2026-06-10
Albertsons tuna salad and Muenster cheese snack pack omits tuna
Albertsons store-made Ready Meals Tuna Salad & Muenster Cheese Snack Pack is being recalled because the contains statement does not declare tuna. 237 units are affected.
Product
UPC 21843300000 READY MEALS TUNA SALAD & MUENSTER CHEESE SNACK PACK This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·H-1056-2026·2026-06-10
Albertsons cajun premium salmon omits salmon from contains statement
Albertsons store-made Salmon Cajun Premium is being recalled because the contains statement does not declare salmon. 41 units are affected.
Product
UPC 21292200000 SALMON CAJUN PREMIUM FS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·H-1065-2026·2026-06-10
Albertsons carne asada marinade salmon fillet omits salmon declaration
Albertsons store-made Salmon Fillet Carne Asada Marinade is being recalled because the contains statement does not declare salmon. Six units are affected.
Product
UPC 23077600000 SALMON FILLET CARNE ASADA MARINADE This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·H-1067-2026·2026-06-10
Albertsons citrus lemon salmon fillet omits salmon declaration
Albertsons store-made Salmon Fillet with Citrus Lemon Marinade is being recalled because the contains statement does not declare salmon.
Product
UPC 23151700000 SALMON FILLET With CITRUS LEMON MARINADE This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2267-2026·2026-06-10
B. Braun spinal epidural kits contain Mastisol with cracking tubing
B. Braun Lyndon B Johnson Hospital spinal epidural kits are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack, rendering it unusable.
Product
Brand Name: B. BRAUN MEDICAL INC. Product Name: LYNDON B JOHNSON HOSPITAL SPINAL EPID Model/Catalog Number: 530184 Software Version: N/A Product Description: LYNDON B JOHNSON HOSPITAL SPINAL EPID Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2285-2026·2026-06-10
Philips Azurion 3M15 Medical Imaging Systems Recalled Due to Software Issue
Philips Medical Systems is recalling 27 Philips Azurion 3M15 units because a software issue can cause unusable dark images during imaging procedures.
Product
Philips Azurion 3M15, Model Numbers: 722064, 722222 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2273-2026·2026-06-10
Covidien 9 Fr Mon-a-Therm temperature probes lack FDA clearance
Covidien Mon-a-Therm general purpose temperature probes in size 9 Fr, REF 90050, are being recalled because the devices lack FDA clearance. 128,900 units are affected.
Product
Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·H-1043-2026·2026-06-10
Albertsons salmon quinoa lentil grain bowl omits salmon declaration
Albertsons store-made Grain Bowl Salmon Quinoa Lentil is being recalled because the contains statement does not declare salmon. Nine units are affected.
Product
UPC 29502200000 Ready Meals BOWL GRAIN SALMON QUINOA LENTIL SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·H-1068-2026·2026-06-10
Albertsons citrus lemon salmon kabobs omit salmon declaration
Albertsons store-made Salmon Kabob with Citrus Lemon Marinade is being recalled because the contains statement does not declare salmon.
Product
UPC 23180600000 SALMON KABOB With CITRUS LEMON MARINADE This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2271-2026·2026-06-10
Covidien esophageal stethoscope temperature sensors lack FDA clearance
Covidien Mon-a-Therm Esophageal Stethoscopes with Temperature Sensor 400TM, REF 90042, are being recalled because the devices lack FDA clearance. 23,000 units are affected.
Product
Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF: 90042
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V379000·2026-06-09
Vermeer Recalls BC1800XL Brush Chipper Trailers Due to Hydraulic Jack Defect
Vermeer is recalling 2002-2026 BC1800XL brush chipper trailers because the hydraulic jack may extend unexpectedly, increasing the risk of loss of vehicle control and injury.
Product
VERMEER — VERMEER BC1800XL
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V371000·2026-06-09
Ford Recalls 2024 Explorers for Potential Park System Damage
Ford is recalling 2024 Explorer vehicles with 2.3L engines and 10R60 transmissions because an unintentional powertrain control module reset may damage the park system, increasing the risk of vehicle rollaway.
Product
FORD — FORD EXPLORER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V369000·2026-06-09
Ford Recalls 2012-2018 Focus Vehicles for Engine Stall Risk
Ford is recalling 2012-2018 Focus vehicles previously repaired under recall 18V735 because a malfunctioning Canister Purge Valve may cause the engine to stall while driving, increasing crash risk.
Product
FORD — FORD FOCUS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V378000·2026-06-09
Ford Recalls 2014 F-150s for Transmission Software Update
Ford is recalling 2014 F-150 vehicles previously repaired under recall 24V444 because a signal loss can cause unexpected downshifting, increasing crash risk.
Product
FORD — FORD F-150
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V376000·2026-06-09
Ford Recalls Focus and Fusion Vehicles for Transmission Clutch Fracture Risk
Ford is recalling 2015-2018 Focus and 2013-2016 Fusion vehicles previously repaired incorrectly under prior recalls. The clutch may fracture, causing transmission damage and fluid leaks that increase fire risk.
Product
FORD — FORD FOCUS, FUSION
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26E033000·2026-06-09
Cummins CNG Fuel System Recall for Tank Bracket Deformation Risk
Natural Gas Fuel Systems is recalling Cummins CNG fuel systems because the tank support bracket may deform in a side impact, potentially causing the tank to detach and leak fuel.
Product
FUEL SYSTEM, OTHER:STORAGE:TANK ASSEMBLY:MOUNTING recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V368000·2026-06-09
Ford Recalls 2018-2024 Expeditions for Center Console Sharp Edges
Ford is recalling 2018-2024 Expedition vehicles because chrome plating on the center console may peel, creating sharp edges that could injure occupants.
Product
FORD — FORD EXPEDITION
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V380000·2026-06-09
Midwest Automotive Design motorhome ground cables may be undersized
Alliance RV is recalling certain Midwest Automotive Design recreational vehicles because the ground wire may be undersized for the electrical system, risking overheating and fire.
Product
MIDWEST AUTOMOTIVE DESIGN — MIDWEST AUTOMOTIVE DESIGN ULTIMATE TRAVELER, PROFESSIONAL SERIES, ATHLETIC SERIES, BUSINESS CLASS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V372000·2026-06-09
Ford Recalls 2019 Mustang, Nautilus, and Navigator for Instrument Cluster Defect
Ford is recalling 2,349 vehicles because the instrument cluster may display blank, hiding critical safety information and increasing crash risk.
Product
LINCOLN — LINCOLN, FORD NAUTILUS, NAVIGATOR, MUSTANG
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V370000·2026-06-09
Ford Recalls 2017 F-150s for Instrument Cluster Power Loss
Ford is recalling 4,445 2017 F-150 vehicles because the instrument cluster may lose power in cold temperatures, hiding critical safety information like gear position.
Product
FORD — FORD F-150
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V375000·2026-06-09
Ford Recalls 2018 F-150s for Transmission Software Defect
Ford is recalling 2018 F-150 vehicles previously repaired under recall 17V669 due to a software defect that may cause unintended gear selection and loss of gear indication.
Product
FORD — FORD F-150
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V377000·2026-06-09
Ford Recalls 2019 Lincoln Nautilus for Lane Center Assist Software Defect
Ford is recalling 2019 Lincoln Nautilus vehicles previously repaired under recall 19V031 because the lane center assist system may fail to detect if the driver's hands are off the steering wheel for a prolonged period.
Product
LINCOLN — LINCOLN NAUTILUS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V373000·2026-06-09
Ford Recalls 2018-2020 F-150s for Daytime Running Lamp Defect
Ford is recalling 2018-2020 F-150 vehicles previously repaired under recall 20V097 because daytime running lamps may fail to dim, reducing visibility for other drivers.
Product
FORD — FORD F-150
Category
Vehicle
Distribution
Distributed nationwide