State

Idaho product recalls

72,986 recalls have nationwide distribution and so reach Idaho. 3,517 additional recalls listed Idaho specifically in their distribution scope.

What the numbers show

Total: 3,517
Critical: 364
Severe: 1,023
Most recent: 2026-09-06

Of the 3,517 recalls naming Idaho we have scored against our rubric, 364 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,023 (29%) are Severe.

Which agencies issued them

These figures cover only the 3,517 recalls whose distribution notice names Idaho specifically. The 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6401–6425 of 76503

HighFDA (Devices)·Z-1925-2025·2025-06-18
Digital Acquisition Box Electrode Placement Labels Applied Backwards
Natus Neurology has recalled the OBM00002 OBM DAB (Digital Acquisition Box) because electrode placement labels were applied backwards. This may lead to misdiagnosis of seizure location in neonates monitored with the device.
Product
Brand Name: OBM00002 OBM DAB (Digital Acquisition Box) Product Name: OBM00002 OBM DAB (Digital Acquisition Box) Model/Catalog Number: OBM00002 OBM DAB (Digital Acquisition Box) Software Version: N/A Product Description: OBM00002 OBM DAB (Digital Acquisition Box) Component: N
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1927-2025·2025-06-18
EPIONE Stereotactic Device Software Bug Poses Instrument Guidance Risk
The EPIONE Model 30-0001 stereotactic device is recalled due to a software bug that may cause the robotic arm to incorrectly guide surgical instruments during CT-guided ablation procedures. Four units have been distributed in the U.S.
Product
EPIONE Model 30-0001 UDI-DI code: 03760305400031 The EPIONE¿ device is a user controlled, stereotactic accessory intended to assist in the planning and manual advancement of one or more instruments, as well as in verification of instrument position during Computed Tomography
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1971-2025·2025-06-18
BD Texium Needle-Free Syringe Recalled for Potential Leakage at Luer Interface
BD Texium Needle-Free Syringes (multiple sizes) may leak at the interface between the male luer component and needle-free connector, potentially causing treatment delays, medication underdosing, or exposure to hazardous drugs.
Product
BD Texium Needle-Free Syringe: 3 mL, REF: MY8003; 5 mL, REF: MY8005; 10 mL, REF: MY8010; 20 mL, REF: MY8020; 30 mL, REF: MY8030; 60 mL, REF: MY8060
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1950-2025·2025-06-18
Tecfen Medical 2.2mm Slit Knife ophthalmic device sterility recall
Tecfen Medical is recalling its 2.2mm Slit Knife (Model QKN2261) due to sterility assurance concerns. The ophthalmic knife is used to create precise incisions for eye surgery.
Product
Brand Name: Tecfen Medical Product Name: 2.2mm Slit Knife, Angled Model/Catalog Number: QKN2261 Software Version: No software Product Description: This is an ophthalmic knife (manual) that is to be sterile (gamma radiation) and packaged individually in Tyvek 1059B. Slit knive
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25C008000·2025-06-18
Evenflo Recalls Titan 65 Child Seats Due to Incorrect Instruction Manuals
Evenflo is recalling Titan 65 child seats manufactured in early 2025 that may have incorrect instruction manuals, posing a risk of improper installation.
Product
EQUIPMENT:OTHER:OWNERS/SERVICE/OTHER MANUAL recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1957-2025·2025-06-18
KWIK-STICK Quality Control Kit for Culture Media Swab Mix-Up
Microbiologics Inc is recalling KWIK-STICK quality control kits because products were packaged with incorrect microorganism swabs, which may lead to delayed diagnosis of patient samples in clinical laboratories.
Product
KWIK-STICK, Quality control kit for culture media, Catalog Numbers 01065K, Oligella urethralis derived from ATCC¿ 17960; 0621K, Staphylococcus aureus derived from NCTC 12493
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1973-2025·2025-06-18
BD TEXIUM Closed Male Luer Drug Transfer Device Recall
BD TEXIUM Closed Male Luer devices may leak at the interface between the closed male luer component and needle-free connector. The leak could cause procedure delays, treatment interruptions, exposure to hazardous drugs, and underdosing of medication.
Product
BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP, REF: 10012241-0500
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1965-2025·2025-06-18
iBOT PMD Personal Mobility Device Software Update Recall
Mobius Mobility LLC is recalling 442 units of the iBOT PMD (Personal Mobility Device) with software version 01.05.24 due to a software issue that could cause the device to tip over during Balance Mode operation.
Product
iBOT PMD with software version 01.05.24. Personal Mobility Device.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1920-2025·2025-06-18
SOLTIVE Pro SuperPulsed Laser System surgical instrument thermal incident
Olympus Corporation of the Americas is recalling the SOLTIVE Pro SuperPulsed Laser System due to risk of unexpected smoke, sparks, burning, or unsteady flames caused by fiber fracturing during clinical use.
Product
Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Pro SuperPulsed Laser System Model/Catalog Number: TFL-SLS, TFL-SLS-JA (Japan only); Product Description: SOLTIVE Laser Systems use technology to increase procedural efficiency and flexibility to ureteroscopy,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1954-2025·2025-06-18
Tecfen Medical 2.0mm Crescent Knife Ophthalmic Device Recall
Tecfen Medical is recalling 2.0mm Crescent Knife ophthalmic surgical instruments (Model QKN1010, Lot ZGY24071501-03) due to sterility assurance concerns. The affected devices were distributed in the US and internationally.
Product
Brand Name: Tecfen Medical Product Name: 2.0mm Crescent Knife Angled Bevel Up Model/Catalog Number: QKN1010 Software Version: No software Product Description: This is an ophthalmic knife (manual) that is to be sterile and packaged individually in Tyhvek 1059B. The crescent kn
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1966-2025·2025-06-18
Allon 2001 Medical Device Heating System Malfunction Risk
Belmont Instrument's Allon 2001 device may heat water above safe limits if sensor connections fail and temperature alarms are disabled. The patient wrap may exceed its set temperature without user notification.
Product
Allon 2001. Part Number: 200-00263
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1970-2025·2025-06-18
Alaris Pump Infusion Sets may leak at male luer connections
BD Switzerland is recalling multiple Alaris Pump Infusion Set models worldwide due to potential leaks at the connection between the closed male luer component and needle-free connector, which could delay procedures, interrupt treatment, expose patients to hazardous drugs, or result in underdosing.
Product
Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded Texium With Priming Cap Back Check Valve 2 SmartSite Y-Sites, REF: 10013361T; SmartSite Bag Access Non-Vented Bonded Texium Closed Male Luer With Priming Cap, REF: 10321213T; SmartSite Bag Access Non-Vented Low
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1949-2025·2025-06-18
Tecfen Medical 15 degree Stab Knife sterility assurance recall
Tecfen Medical is recalling its 15 degree Stab Knife (Model QKN1501) due to sterility assurance concerns. The ophthalmic knife is used in eye surgeries and was distributed in the US and internationally.
Product
Brand Name: Tecfen Medical Product Name: 15 degree Stab Knife Model/Catalog Number: QKN1501 Software Version: No software Product Description: This is an ophthalmic knife (manual) that is to be sterile (gamma radiation) and packaged individually in Tyvek 1059B. Stab knives ar
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1939-2025·2025-06-18
Femoral Nail T2 GTN Left and Right Versions Mislabeled
Stryker GmbH is recalling certain Femoral Nail T2 GTN devices because some labeled as left version contained right nails, and vice versa. This mislabeling could result in incorrect surgical implantation.
Product
Femoral Nail, LEFT T2 GTN 8x300 mm. Catalog Number: 1850-0830S.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V418000·2025-06-18
Mazda Recalls 2025 CX-50 Hybrid for Gear Shifter Safety Issue
Mazda is recalling 2025 CX-50 Hybrid vehicles because the gear shifter can move to Drive without pressing the brake pedal, increasing crash risk.
Product
MAZDA — MAZDA CX-50 HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0934-2025·2025-06-18
Instant Milk Tea Powder lacks milk allergen declaration
R&M Trading LLC is recalling Instant Milk Tea Original Flavor because the label does not declare milk, despite containing whey powder and sodium caseinate, which are milk-derived ingredients.
Product
Instant Milk Tea Original Flavor, R&M Refresher brand, B0D71YHZX4, net wt. 1lb. Product is sold in 1-pack or 3-pack. Parent ASIN #B0D728CZWS 1-pack ASIN #B0D71YHZX4 3-pack ASIN #B0D72BLQRW Label declares Ingredients: Non-Dairy Creamer (Glucose Syrup, Vegetable Oil, Whey Powder
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0935-2025·2025-06-18
Instant Milk Tea Brown Sugar Powder recalled for undeclared milk allergen
R&M Refresher brand Instant Milk Tea Brown Sugar Flavor is recalled because the ingredients contain milk (Whey Powder, Sodium Caseinate) but the label does not declare milk as an allergen.
Product
Instant Milk Tea Brown Sugar Flavor, R&M Refresher brand, B0D725TXQW, net wt. 1lb. Product is sold in 3-pack. Parent ASIN #B0D728CZWS 3-pack ASIN #B0D72FQVDR Ingredients: Non-Dairy Creamer (Glucose Syrup, Vegetable Oil, Whey Powder, Sodium Caseinate***). Product of China. Dis
Category
Food
Distribution
Distributed nationwide
HighNHTSA·25V410000·2025-06-18
2026 Tesla Model Y and Model 3 Vehicles Seat Fastener Recall
Tesla is recalling certain 2026 Model Y and Model 3 vehicles because seat back fasteners may have been improperly tightened, potentially affecting proper occupant restraint during a crash.
Product
TESLA — TESLA MODEL 3, MODEL Y
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1923-2025·2025-06-18
Soltive Reusable Laser Fibers Recalled for Thermal Incident Risk
Olympus Corporation of the Americas is recalling Soltive Reusable Laser Fibers due to risk of thermal incidents including smoke, sparks, burning, or unsteady flames during surgery, caused by fiber fracturing.
Product
Brand Name: Powered Laser Surgical Instrument Product Name: Soltive Reusable Laser Fibers Model/Catalog Number: TFL-FBX150R, TFL-FBX200R, TFL-FBX365R, TFL-FBX550R, TFL-FBX940R, TFL-FBX940R-JA (Japan Only), TFL-FBX365R-JA (Japan Only), TFL-FBX200BS-JA (Japan Only), TFL-FBX150R-J
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1955-2025·2025-06-18
Tecfen Medical 3.2mm Slit Knife Angled Ophthalmic Knife Sterility Recall
Tecfen Medical is recalling the 3.2mm Slit Knife, Angled model QKN3261 due to sterility assurance concerns. The recall affects units distributed nationwide in Connecticut and Minnesota as well as internationally.
Product
Brand Name: Tecfen Medical Product Name: 3.2mm Slit Knife, Angled Model/Catalog Number: QKN3261 Software Version: No software Product Description: This is an ophthalmic knife (manual) that is to be sterile and packaged individually in Tyvek 1059B. Slit knives are used to crea
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V416000·2025-06-18
REV Recalls 2025-2026 Fleetwood and Holiday Rambler Motorhomes for Electrical Defect
REV is recalling 2025-2026 Fleetwood Altitude and Holiday Rambler Incline motorhomes because water intrusion may cause electrical components to fail, potentially disabling carbon monoxide or propane detectors.
Product
FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER ALTITUDE, INCLINE
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·25343·2025-06-18
Polaris Ranger XP and Pro XD Kinetic ROVs Recalled for Fire Hazard
Polaris is recalling Model Year 2023-2024 Ranger XP Kinetic and Model Year 2025 Pro XD Kinetic ROVs because water can leak through a cracked filter into the high-voltage charging harness and cause a fire. The company has received 47 reports of filter failures, including six reports of melting or fire.
Product
Model Year 2023-2024 Ranger XP Kinetic and Model Year 2025 Pro XD Kinetic ROVs
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·25341·2025-06-18
YaFiti White 12-Drawer Dressers Recalled for Tip-Over Entrapment Hazards
YaFiti 12-Drawer White Dressers pose serious tip-over and entrapment hazards to children if not anchored to the wall, violating federal standards. About 6,000 units sold on Amazon from September 2023 through March 2025.
Product
YaFiti 12-Drawer White Dressers
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0468-2025·2025-06-18
Cephalexin Oral Suspension Recalled for Failed Impurity Specifications
Ascend Laboratories is recalling Cephalexin for Oral Suspension due to failed impurity specifications identified during stability testing. An out-of-specification result for Cephalexin Glucose Adduct was observed at six months.
Product
CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0932-2025·2025-06-18
Instant Milk Tea Taro Flavor Recalled for Undeclared Milk Allergen
R&M Refresher brand Instant Milk Tea Powder in Taro Flavor is recalled nationwide because the label does not declare milk, though the product contains Whey Powder and Sodium Caseinate derived from milk.
Product
Instant Milk Tea Taro Flavor, R&M Refresher brand, B0D72CMLBH, net wt. 1lb. Product was sold in 1-pack or 3-pack. Parent ASIN #B0D728CZWS 1-pack ASIN #B0D72CMLBH 3-pack ASIN #B0D72D6589 Label declares Ingredients: Non-Dairy Creamer (Glucose Syrup, Vegetable Oil, Whey Powder,
Category
Food
Distribution
Distributed nationwide