Latest recalls — page 10

Soba sauce packet, which contains bonito, sardine, and mackerel (fish), was packed into Sura Tanmen Hot and Sour Flavor ramen noodle package kit, but fish species are not declared …

Company / brand: H & U dba Sun Noodle recalls

Official ID H-1258-2026 · Official record ↗

FDA Class I · Drug · September 2, 2026

Lactated Ringer's Injection USP recall — B BRAUN MEDICAL INC

Presence of Particulate matter.

Company / brand: B BRAUN MEDICAL recalls

Official ID D-0832-2026 · Official record ↗

FDA Class II · Drug · September 2, 2026

Ramipril Capsules USP recall — Hikma Pharmaceuticals USA INC.

Failed Impurities/Degradation Specifications: OOS result obtained for a process impurity, dicyclohexylurea (DCU).

Company / brand: Hikma Pharmaceuticals USA recalls

Official ID D-0831-2026 · Official record ↗

FDA Class I · Drug · September 2, 2026

Tyenne (tocilizumab-aazg) Injection recall — Fresenius Kabi USA, LLC

Presence of particulate matter:An internal investigation at the firm found the product to contain glass particles.

Company / brand: Fresenius Kabi USA recalls

Official ID D-0827-2026 · Official record ↗

FDA Class II · Drug · September 2, 2026

Paxil CR recall — Apotex Corp.

Failed Dissolution Specifications; product failed to meet 24-month stability testing acceptance criteria

Company / brand: Apotex recalls

Official ID D-0804-2026 · Official record ↗

FDA Class II · Drug · September 2, 2026

Acthar Gel (repository corticotropin injection) recall — Mallinckrodt Hospital Products Inc.

Presence of particulate matter: glass and stopper piece

Company / brand: Mallinckrodt Hospital Products recalls

Official ID D-0803-2026 · Official record ↗

FDA Class II · Drug · September 2, 2026

Zicam recall — Church & Dwight Co., Inc.

CGMP Deviations; FDA inspection of the contract manufacturer noted out of limit results for microbiological testing

Company / brand: Church & Dwight Co recalls

Official ID D-0790-2026 · Official record ↗

FDA Class II · Drug · September 2, 2026

Clobetasol Propionate Cream USP recall — Lupin Pharmaceuticals Inc.

Failed content uniformity specifications.

Company / brand: Lupin Pharmaceuticals recalls

Official ID D-0789-2026 · Official record ↗

FDA Class II · Drug · September 2, 2026

Levothyroxine Sodium Tablets recall — ACCORD HEALTHCARE, INC.

Subpotent Drug

Company / brand: ACCORD HEALTHCARE recalls

Official ID D-0786-2026 · Official record ↗

FDA Class II · Drug · September 2, 2026

Levothyroxine Sodium Tablets recall — ACCORD HEALTHCARE, INC.

Subpotent Drug

Company / brand: ACCORD HEALTHCARE recalls

Official ID D-0785-2026 · Official record ↗

FDA Class II · Drug · September 2, 2026

Levothyroxine Sodium Tablets recall — ACCORD HEALTHCARE, INC.

Subpotent Drug

Company / brand: ACCORD HEALTHCARE recalls

Official ID D-0784-2026 · Official record ↗

FDA Class II · Drug · September 2, 2026

Levothyroxine Sodium Tablets recall — ACCORD HEALTHCARE, INC.

Subpotent Drug

Company / brand: ACCORD HEALTHCARE recalls

Official ID D-0783-2026 · Official record ↗

FDA Class II · Drug · September 2, 2026

Levothyroxine Sodium Tablets recall — ACCORD HEALTHCARE, INC.

Subpotent Drug

Company / brand: ACCORD HEALTHCARE recalls

Official ID D-0782-2026 · Official record ↗

FDA Class II · Drug · September 2, 2026

Levothyroxine Sodium Tablets recall — ACCORD HEALTHCARE, INC.

Subpotent Drug

Company / brand: ACCORD HEALTHCARE recalls

Official ID D-0781-2026 · Official record ↗

FDA Class II · Drug · September 2, 2026

Levothyroxine Sodium Tablets recall — ACCORD HEALTHCARE, INC.

Subpotent Drug

Company / brand: ACCORD HEALTHCARE recalls

Official ID D-0780-2026 · Official record ↗

FDA Class II · Drug · September 2, 2026

Levothyroxine Sodium Tablets recall — ACCORD HEALTHCARE, INC.

Subpotent Drug

Company / brand: ACCORD HEALTHCARE recalls

Official ID D-0779-2026 · Official record ↗

FDA Class II · Drug · September 2, 2026

Levothyroxine Sodium Tablets recall — ACCORD HEALTHCARE, INC.

Subpotent Drug

Company / brand: ACCORD HEALTHCARE recalls

Official ID D-0778-2026 · Official record ↗

FDA Class II · Drug · September 2, 2026

Levothyroxine Sodium Tablets recall — ACCORD HEALTHCARE, INC.

Subpotent Drug

Company / brand: ACCORD HEALTHCARE recalls

Official ID D-0777-2026 · Official record ↗

FDA Class II · Drug · September 2, 2026

Levothyroxine Sodium Tablets recall — ACCORD HEALTHCARE, INC.

Subpotent Drug

Company / brand: ACCORD HEALTHCARE recalls

Official ID D-0776-2026 · Official record ↗

FDA Class II · Drug · September 2, 2026

Levothyroxine Sodium Tablets recall — ACCORD HEALTHCARE, INC.

Subpotent Drug

Company / brand: ACCORD HEALTHCARE recalls

Official ID D-0775-2026 · Official record ↗

NHTSA · Vehicle · September 1, 2026

Peterbilt 548 recall (26V567000)

Delayed brake response time can increase the risk of a crash.

Company / brand: Paccar Incorporated recalls

Official ID 26V567000 · Official record ↗

NHTSA · Vehicle · September 1, 2026

Storyteller Overland Electrical System recall (26V566000)

An overheated printed circuit board increases the risk of a fire.

Company / brand: Storyteller Overland recalls

Official ID 26V566000 · Official record ↗

NHTSA · Vehicle · September 1, 2026

Forest River Bus Equipment Adaptive/Mobility recall (26V565000)

A wheelchair lift that continues to move while occupied increases the risk of injury.

Company / brand: Forest River Bus recalls

Official ID 26V565000 · Official record ↗

NHTSA · Vehicle · September 1, 2026

Light Boy GBX12SK recall (26V564000)

A detach light tower can become a road hazard for other vehicles, increasing the risk of a crash or injury.

Company / brand: Light Boy America recalls

Official ID 26V564000 · Official record ↗

NHTSA · Vehicle · September 1, 2026

Forest River Vibe recall (26V563000)

Unvented exhaust fumes increase the risk of injury from carbon monoxide poisoning.

Company / brand: Forest River recalls

Official ID 26V563000 · Official record ↗

NHTSA · Vehicle · September 1, 2026

Chrysler Suspension recall (26V562000)

Rear coil springs that detach from the vehicle while driving increase the risk of a crash.

Company / brand: Chrysler recalls

Official ID 26V562000 · Official record ↗

NHTSA · Vehicle · September 1, 2026

Chrysler Electronic Stability Control (Esc) recall (26V561000)

A loss of electronic stability control increases the risk of a crash.

Company / brand: Chrysler recalls

Official ID 26V561000 · Official record ↗

NHTSA · Vehicle · September 1, 2026

Ram 1500 recall (26V560000)

A rearview image that does not display reduces the driver's view behind the vehicle, increasing the risk of a crash.

Company / brand: Chrysler recalls

Official ID 26V560000 · Official record ↗

NHTSA · Vehicle · September 1, 2026

Chrysler Tires recall (26V559000)

A TPMS warning light that fails to notify the driver of low tire pressure increases the risk of a crash.

Company / brand: Chrysler recalls

Official ID 26V559000 · Official record ↗

NHTSA · Vehicle · September 1, 2026

Tesla Model Y recall (26V558000)

A lateral link separation could shift the wheel alignment, causing a loss of vehicle control and increasing the risk of a crash.

Company / brand: Tesla recalls

Official ID 26V558000 · Official record ↗

NHTSA · Vehicle · August 31, 2026

Tiffin Wayfarer recall (26V557000)

LP tanks that cannot be shut off increase the risk of a fire. Additionally a loose LP tank may detach and become a road hazard, increasing the risk of a crash.

Company / brand: Tiffin Motorhomes recalls

Official ID 26V557000 · Official record ↗

NHTSA · Vehicle · August 31, 2026

Blue Bird Vision School Bus recall (26V556000)

A wheelchair lift that continues to move while occupied increases the risk of injury.

Company / brand: Blue Bird Body Company recalls

Official ID 26V556000 · Official record ↗

NHTSA · Vehicle · August 31, 2026

Jayco Electrical System recall (26V555000)

The incorrect warning light may fail to alert the driver to critical safety information or cause confusion, increasing the risk of a crash.

Company / brand: Jayco recalls

Official ID 26V555000 · Official record ↗

NHTSA · Vehicle · August 31, 2026

Jayco Equipment recall (26V554000)

Incorrect information may result in the wrong sized replacement tires being installed, increasing the risk of a crash.

Company / brand: Jayco recalls

Official ID 26V554000 · Official record ↗

NHTSA · Vehicle · August 28, 2026

Magic Tilt Aluminum Watercraft Trailer recall (26V553000)

A detached winch may increase the risk of injury to people near the trailer.

Company / brand: Magic Tilt Trailers recalls

Official ID 26V553000 · Official record ↗

NHTSA · Vehicle · August 28, 2026

Heartland Bighorn recall (26V552000)

Referencing the incorrect weight could result in the trailer being overloaded, increasing the risk of a crash.

Company / brand: Jayco recalls

Official ID 26V552000 · Official record ↗

NHTSA · Vehicle · August 27, 2026

Altec Service Body recall (26V551000)

An electrical short circuit can increase the risk of a fire.

Company / brand: Altec Industries recalls

Official ID 26V551000 · Official record ↗

CPSC · Toys · August 27, 2026

Montessori Baby Toy Sets Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon by Chillife Official

The recalled baby toy sets contain a pull string teething toy that violates the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The …

Company / brand: Shenzhenshixingchuangyiyimaoyouxiangongsi (Shenzhen Xingchuangyi Trading Co recalls

Official ID 26727 · Official notice ↗

CPSC · Desks, Dressers, Chests, Bureaus, Or Buffets · August 27, 2026

Walmart Reannounces Recall of Mainstays Nine-Drawer Fabric Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Walmart Distributed Recalled Dressers Post-Recall; Sold to Consumers Through Liquidators

The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risk of serious injuries or death to children. Th…

Company / brand: Hop Thang Interior Wood Co recalls

Official ID 26726 · Official notice ↗

CPSC · Pressure Washers · August 27, 2026

Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Sold on Amazon by YERYORK

The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI) and an adequate-length power cord, posing serious risks of injury or death from shock and ele…

Company / brand: Lanzhou Xinshi Mingchen Information Technology Co recalls

Official ID 26725 · Official notice ↗

CPSC · Clothing · August 27, 2026

Little Loves & Co. Recalls Youth Clothing with Drawstrings Due to Risk of Serious Injury or Death from Entrapment Hazard

The drawstrings in the recalled clothing can get caught on objects and cause death or serious injury to children due to an entrapment hazard.

Company / brand: Little Loves & Co recalls

Official ID 26724 · Official notice ↗

CPSC · Pressure Washers · August 27, 2026

Steelite Pressure Washers Recalled Due to Risk of Serious Injury or Death from Shock and Electrocution Hazards; Sold on Amazon by Longer 3D

The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI) and an adequate-length power cord, posing a risk of serious injury or death from shock and el…

Company / brand: Longer Technology (Hong Kong) recalls

Official ID 26723 · Official notice ↗

CPSC · Lights & Accessories · August 27, 2026

Excel Industries Recalls Accessory LED Light Kits Due to Risk of Serious Injury from Fire Hazard

The light bars can overheat or produce flames, posing a risk of serious injury from a fire hazard.

Company / brand: Excel Industries recalls

Official ID 26722 · Official notice ↗

CPSC · Baby Walkers Or Jumpers · August 27, 2026

Kmaier Recalls Infant Walkers Due to Risk of Serious Injury or Death from Fall Hazard; Violate Mandatory Standard for Infant Walkers

The recalled walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a step, posing a deadly fall …

Company / brand: FENUN recalls

Official ID 26721 · Official notice ↗

CPSC · Hi-Fi And Stereo Equip., Amplifiers, Speakers · August 27, 2026

AudioLineOut Recalls Studio Six Headphone Amplifiers Due to Risk of Serious Injury or Death from Electrocution Hazard

When the amplifiers are used with aftermarket metal base tubes, the bare metal can become electrified, posing a risk of serious injury or death from electrocution.

Company / brand: AudioLineOut recalls

Official ID 26720 · Official notice ↗

CPSC · Toys · August 27, 2026

HABA USA Recalls Rainbow Rattle Grasping and Teething Toys Due to Risk of Serious Injury or Death from Choking and Ingestion Hazards

The glued knot on the elastic cord can become untied on the recalled product, allowing young children access to the small wooden and plastic pieces, posing a risk of serious injury…

Company / brand: Habermaass recalls

Official ID 26719 · Official notice ↗

CPSC · Towels Or Cloths · August 27, 2026

Diamond Wipes International Recalls MD Wipe Outz Numbing Tattoo Wipes Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging

The recalled numbing wipes contain lidocaine, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The packaging of the wipes is not chil…

Company / brand: Diamond Wipes International recalls

Official ID 26718 · Official notice ↗

CPSC · Cleaning Equipment, Inc. Brooms, Mops, Brushes, Etc · August 27, 2026

Conair Expands Recall of Cuisinart Grill Brushes Due to Ingestion Hazard; Over 3.6 Million Brushes Now Recalled

Small metal wire bristles can detach from the brushes and stick to the grill or food, posing an ingestion hazard and risk of serious internal injuries that could require surgery.

Company / brand: Conair of Stamford recalls

Official ID 26717 · Official notice ↗

NHTSA · Vehicle equipment · August 26, 2026

Bell Sports recall (26E061000)

A helmet that does not provide adequate impact protection increases the risk of injury in a crash.

Company / brand: Bell Sports recalls

Official ID 26E061000 · Official record ↗

FDA Class II · Medical device · August 26, 2026

American Contract Systems medical procedure kits and trays labeled as recall — American Contract Systems Inc

The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998…

Company / brand: American Contract Systems recalls

Official ID Z-2990-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026

American Contract Systems medical procedure kits and trays labeled as recall — American Contract Systems Inc

The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998…

Company / brand: American Contract Systems recalls

Official ID Z-2989-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026

Brand Name recall — restor3d Inc.

Due to incorrect machining of peripheral screw hole resulting in potential for improper engagement of the peripheral screws.

Company / brand: restor3d recalls

Official ID Z-2987-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026

Esteem Body Soft Convex Urostomy Pouch Model/Catalog Numbers recall — ConvaTec, Inc

Urostomy Pouches may leak from cap during use.

Company / brand: ConvaTec recalls

Official ID Z-2986-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026

Fort Defiance Industries (FDI) recall — Fort Defiance Industries, LLC

The Automated Field Steam Sterilizer's water recovery system 120V Amphenol connector may experience an intermittent loss of ground continuity, which could result in an unreliable f…

Company / brand: Fort Defiance Industries recalls

Official ID Z-2983-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026

MiniMed 780G Insulin Pump recall — Medtronic MiniMed, Inc.

Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result in insulin over- or u…

Company / brand: Medtronic MiniMed recalls

Official ID Z-2982-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026

MiniMed 670G Insulin Pump recall — Medtronic MiniMed, Inc.

Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result in insulin over- or u…

Company / brand: Medtronic MiniMed recalls

Official ID Z-2981-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026

MiniMed 640G Insulin Pump recall — Medtronic MiniMed, Inc.

Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result in insulin over- or u…

Company / brand: Medtronic MiniMed recalls

Official ID Z-2980-2026 · Official record ↗

FDA Class I · Medical device · August 26, 2026

BMC/REACTHEALTH Luna G3 APAP REF LG 3600 recall — BMC Medical Co., Ltd.

Retroactive reporting for 2024 rework conducted at the 3B/React Health warehouse

Company / brand: BMC Medical Co recalls

Official ID Z-2979-2026 · Official record ↗

FDA Class I · Medical device · August 26, 2026

Boston Scientific ENROUTE Transcarotid Neuroprotection System Plus recall — Boston Scientific Corporation

Potential for arterial sheath tip separation or partial tip separation during use.

Company / brand: Boston Scientific recalls

Official ID Z-2978-2026 · Official record ↗

FDA Class I · Medical device · August 26, 2026

Boston Scientific ENROUTE Transcarotid Neuroprotection System recall — Boston Scientific Corporation

Potential for arterial sheath tip separation or partial tip separation during use.

Company / brand: Boston Scientific recalls

Official ID Z-2977-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026

Beckman Coulter recall — Siemens Healthcare Diagnostics, Inc.

Due to unacceptable precision performance exhibited in certain lots of the Emit 2000 Quinidine Assay, which may lead to erroneously elevated quinidine measurements, creating risk o…

Company / brand: Siemens Healthcare Diagnostics recalls

Official ID Z-2976-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026

Syva EMIT 2000 Quinidine Assay REF recall — Siemens Healthcare Diagnostics, Inc.

Due to unacceptable precision performance exhibited in certain lots of the Emit 2000 Quinidine Assay, which may lead to erroneously elevated quinidine measurements, creating risk o…

Company / brand: Siemens Healthcare Diagnostics recalls

Official ID Z-2975-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026

Beckman Coulter DxC 500 AU Clinical Analyzer Modules using software version 1 recall — Beckman Coulter Inc.

a software defect in which the Parameter Package (PP) import logic overwrites all predefined calculated test rules, including those previously modified by the user, upon import of …

Company / brand: Beckman Coulter recalls

Official ID Z-2974-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026

Beckman Coulter DxC 500i Clinical Analyzer Modules using software version 1 recall — Beckman Coulter Inc.

a software defect in which the Parameter Package (PP) import logic overwrites all predefined calculated test rules, including those previously modified by the user, upon import of …

Company / brand: Beckman Coulter recalls

Official ID Z-2973-2026 · Official record ↗

FDA Class III · Medical device · August 26, 2026

Custom Made Device Implant 6123 Navicular Cage Nominal Right Rev A recall — Paragon 28, Inc.

Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material ductility.

Company / brand: Paragon 28 recalls

Official ID Z-2972-2026 · Official record ↗

FDA Class III · Medical device · August 26, 2026

Custom Made Device Implant 6123 Navicular Cage Small Right Rev A recall — Paragon 28, Inc.

Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material ductility.

Company / brand: Paragon 28 recalls

Official ID Z-2971-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026

Blanketrol III recall — Gentherm Medical, LLC

Overheating of the 115V CPU board may cause the device to shut down.

Company / brand: Gentherm Medical recalls

Official ID Z-2970-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026

Innercool Coolblue Console recall — Gentherm Medical, LLC

Overheating of the 115V CPU board may cause the device to shut down.

Company / brand: Gentherm Medical recalls

Official ID Z-2969-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026

Blanketrol II Model 222S recall — Gentherm Medical, LLC

Overheating of the 115V CPU board may cause the device to shut down.

Company / brand: Gentherm Medical recalls

Official ID Z-2968-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026

Paragonix Technologies Inc recall — Paragonix Technologies Inc.

Due to a firmware defect, the portable organ transfer device datalogger may lose its configuration, resulting in a blank screen and loss of displayed preservation parameters.

Company / brand: Paragonix Technologies recalls

Official ID Z-2967-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026

Siemens Healthineers Immulite 2000 Systems SYP Syphilis Screen REF(s) recall — Siemens Healthcare Diagnostics Products Ltd.

Syphilis Screen assay may contain a negative patient bias resulting in low reactive patient results being reported as nonreactive.

Company / brand: Siemens Healthcare Diagnostics Products recalls

Official ID Z-2966-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026

Siemens Healthineers Immulite 2000 Systems SYP Syphilis Screen REF recall — Siemens Healthcare Diagnostics Products Ltd.

Syphilis Screen assay may contain a negative patient bias resulting in low reactive patient results being reported as nonreactive.

Company / brand: Siemens Healthcare Diagnostics Products recalls

Official ID Z-2965-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026

Halyard LAVH PACK recall — AVID Medical, Inc.

The kit component was subjected to EO sterilization, contrary to the manufacturer recommendation, which may have led to the component leaking in a kit.

Company / brand: AVID Medical recalls

Official ID Z-2964-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026

GETINGE Y SENSOR Module recall — Maquet Critical Care AB

The module did not undergo electrical safety tests and functional tests during production.

Company / brand: Maquet Critical Care AB recalls

Official ID Z-2963-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026

Suture Cinch Long 1pk recall — Boston Scientific Corporation

Device may fail to deploy the cinch implant and/or fail to cut the suture as intended.

Company / brand: Boston Scientific recalls

Official ID Z-2962-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026

OverStitch Suture Cinch recall — Boston Scientific Corporation

Device may fail to deploy the cinch implant and/or fail to cut the suture as intended.

Company / brand: Boston Scientific recalls

Official ID Z-2961-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026

TD Navio Maxi Speech Generating Device Model/Catalog Number recall — Tobii Dynavox Llc

Under certain conditions, the battery mounting tabs may become damaged, allowing the battery to move within the device enclosure, potentially leading to an internal short circuit. …

Company / brand: Tobii Dynavox recalls

Official ID Z-2960-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026

TD Navio Midi Speech Generating Device Model/Catalog Number recall — Tobii Dynavox Llc

Under certain conditions, the battery mounting tabs may become damaged, allowing the battery to move within the device enclosure, potentially leading to an internal short circuit. …

Company / brand: Tobii Dynavox recalls

Official ID Z-2959-2026 · Official record ↗

FDA Class II · Medical device · August 26, 2026