Fresh Recalls

Latest recalls — page 29

Browse the most recent U.S. safety recalls in our connected official government data.

3,525 recalls in our current data. Showing 2,801–2,900, newest first.

FDA Class I · Food · May 27, 2026

GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX FROZEN HOT COCOA NET WT 50oz (3lbs 2oz) 1 recall — Ghirardelli Chocolate Company

Potential contamination with Salmonella.

Company / brand: Ghirardelli Chocolate Company recalls

Official ID H-0838-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

Fisher Tex Mex Trail Mix 30 oz plastic jar UPC 070690275941 recall — JOHN B SANFILIPPO & SONS INC

potential presence of Salmonella

Company / brand: JOHN B SANFILIPPO & SONS recalls

Official ID H-0836-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

Good & Gather Mexican Street Corn Trail Mix 8 oz bag UPC 085239270240 recall — JOHN B SANFILIPPO & SONS INC

potential presence of Salmonella

Company / brand: JOHN B SANFILIPPO & SONS recalls

Official ID H-0835-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

Squirrel Brand Town & Country Mix 16 oz can UPC 07223805251 and 7 recall — JOHN B SANFILIPPO & SONS INC

potential presence of Salmonella

Company / brand: JOHN B SANFILIPPO & SONS recalls

Official ID H-0834-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

Squirrel Brand Travelers Mix 16 oz can UPC 07223899166 recall — JOHN B SANFILIPPO & SONS INC

potential presence of Salmonella

Company / brand: JOHN B SANFILIPPO & SONS recalls

Official ID H-0833-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

Southern Style Nuts Hunter Mix 30 oz plastic jar UPC 085839916302 recall — JOHN B SANFILIPPO & SONS INC

potential presence of Salmonella

Company / brand: JOHN B SANFILIPPO & SONS recalls

Official ID H-0832-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

Southern Style Nuts Gourmet Hunter Mix 23 oz plastic jar UPC 085839073319 and 36 oz plasti recall — JOHN B SANFILIPPO & SONS INC

potential presence of Salmonella

Company / brand: JOHN B SANFILIPPO & SONS recalls

Official ID H-0831-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

Pork King Good Onion & Sour Cream Seasoning recall — Pork King Good, LLC

Seasoning was made with recalled California Dairies milk powder due to Salmonella contamination.

Company / brand: Pork King Good recalls

Official ID H-0830-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

Solina 6022487 Garlic Herb Topping recall — Solina U.S. Holding

potential to be contaminated with Salmonella

Company / brand: Solina U.S. Holding recalls

Official ID H-0829-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

YT 6027393 Spicy Ranch Blend recall — Solina U.S. Holding

potential to be contaminated with Salmonella

Company / brand: Solina U.S. Holding recalls

Official ID H-0828-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

Solina 6036087 Cr¿me Fraiche Spice Seasoning recall — Solina U.S. Holding

potential to be contaminated with Salmonella

Company / brand: Solina U.S. Holding recalls

Official ID H-0827-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

Solina 6036277 Garlic Cream Sauce Seasoning recall — Solina U.S. Holding

potential to be contaminated with Salmonella

Company / brand: Solina U.S. Holding recalls

Official ID H-0826-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

Solina 6036786 Instant Country Gravy Seasoning recall — Solina U.S. Holding

potential to be contaminated with Salmonella

Company / brand: Solina U.S. Holding recalls

Official ID H-0825-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

Solina 6036554 Parmesan Breadstick Sauce Seasoning recall — Solina U.S. Holding

potential to be contaminated with Salmonella

Company / brand: Solina U.S. Holding recalls

Official ID H-0824-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

Solina 6036443 Cheddar Cheese Powder Seasoning recall — Solina U.S. Holding

potential to be contaminated with Salmonella

Company / brand: Solina U.S. Holding recalls

Official ID H-0823-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

Solina 6036195 Ranch Seasoning recall — Solina U.S. Holding

potential to be contaminated with Salmonella

Company / brand: Solina U.S. Holding recalls

Official ID H-0822-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

Solina 6035687 Bayou Blackened Ranch Seasoning recall — Solina U.S. Holding

potential to be contaminated with Salmonella

Company / brand: Solina U.S. Holding recalls

Official ID H-0821-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

Solina 6035415 Sourdough Cheese Crouton Seasoning recall — Solina U.S. Holding

potential to be contaminated with Salmonella

Company / brand: Solina U.S. Holding recalls

Official ID H-0820-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

Non Fat Dry Milk 1# recall — PS Seasoning & Spices, Inc.

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

Company / brand: PS Seasoning & Spices recalls

Official ID H-0819-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

PSW21585 Save A Lot Bind 50# recall — PS Seasoning & Spices, Inc.

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

Company / brand: PS Seasoning & Spices recalls

Official ID H-0818-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

Blackstone Parmesan Ranch Seasoning recall — PS Seasoning & Spices, Inc.

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

Company / brand: PS Seasoning & Spices recalls

Official ID H-0817-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

1P Jalapeno Heat Unit for 300 lbs of Meat recall — PS Seasoning & Spices, Inc.

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

Company / brand: PS Seasoning & Spices recalls

Official ID H-0816-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

1P Original Smokehouse Unit for 300 lbs recall — PS Seasoning & Spices, Inc.

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

Company / brand: PS Seasoning & Spices recalls

Official ID H-0815-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

Ellsworth Sour Cream + Onion Seasoning recall — PS Seasoning & Spices, Inc.

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

Company / brand: PS Seasoning & Spices recalls

Official ID H-0814-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

C7139D1 Natural Parmesan Cheese Flavor recall — Fontana Flavors, Inc

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

Company / brand: Fontana Flavors recalls

Official ID H-0813-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

VG7274D1 Natural Cream of Mushroom Type Flavor recall — Fontana Flavors, Inc

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

Company / brand: Fontana Flavors recalls

Official ID H-0812-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

C0017D Natural & Artificial White Cheddar Cheese Flavor recall — Fontana Flavors, Inc

Product was made with milk powder recalled by the supplier due to Salmonella contamination.

Company / brand: Fontana Flavors recalls

Official ID H-0811-2026 · Official record ↗

FDA Class I · Food · May 27, 2026

MA Cohen's Kippered Herring vacuum packed recall — Shining Sea Fish Co. LLC

Clostridium botulinum is an uncontrolled hazard

Company / brand: Shining Sea Fish Co recalls

Official ID H-0810-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Vitamin B-Complex recall — Llorens Pharmaceuticals International Division, Inc.

Foreign object: black particulate matter

Company / brand: Llorens Pharmaceuticals International Division recalls

Official ID H-0809-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Liposomal Sleep Spray recall — Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

Company / brand: Wellnov Supplements recalls

Official ID H-0808-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Liposomal B12 Spray recall — Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

Company / brand: Wellnov Supplements recalls

Official ID H-0807-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Liposomal D3+B12 Spray recall — Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

Company / brand: Wellnov Supplements recalls

Official ID H-0806-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Liposomal D3-5000IU Spray Dosage recall — Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

Company / brand: Wellnov Supplements recalls

Official ID H-0805-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Liposomal Prenatal+Postnatal Liquid Multivitamin Drops - Iron Free recall — Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

Company / brand: Wellnov Supplements recalls

Official ID H-0804-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Liposomal Women's Liquid Multivitamin Drops - Iron Free recall — Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

Company / brand: Wellnov Supplements recalls

Official ID H-0803-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Liposomal Kids Liquid Multivitamin Drops recall — Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

Company / brand: Wellnov Supplements recalls

Official ID H-0802-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Liposomal Collagen Booster recall — Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

Company / brand: Wellnov Supplements recalls

Official ID H-0801-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Liposomal Women's Liquid Multivitamin Drops with Iron recall — Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

Company / brand: Wellnov Supplements recalls

Official ID H-0800-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Liposomal Mens 50+ Liquid Multivitamin Drops recall — Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

Company / brand: Wellnov Supplements recalls

Official ID H-0799-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Liposomal Mens Liquid Multivitamin Drops recall — Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

Company / brand: Wellnov Supplements recalls

Official ID H-0798-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Liposomal Womens 50+ Liquid Multivitamin Drops recall — Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

Company / brand: Wellnov Supplements recalls

Official ID H-0797-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

FulviLife Complex recall — Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.

Company / brand: Wellnov Supplements recalls

Official ID H-0796-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Joint Nourish recall — Wellnov Supplements LLC

Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen contamination and possible C. Botulinum concerns.

Company / brand: Wellnov Supplements recalls

Official ID H-0795-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Liquid Blenz Good Brain Tonic 16 oz and 32 oz recall — LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

Company / brand: LIQUID BLENZ recalls

Official ID H-0794-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Flat Belly Bully 16 oz and 32 oz recall — LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

Company / brand: LIQUID BLENZ recalls

Official ID H-0793-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Blood Pressure Bully 16 oz and 32 oz recall — LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

Company / brand: LIQUID BLENZ recalls

Official ID H-0792-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Pure Shilajit Tonic 16 oz and 32 oz recall — LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

Company / brand: LIQUID BLENZ recalls

Official ID H-0791-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Prostate Bully 16 oz and 32 oz recall — LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

Company / brand: LIQUID BLENZ recalls

Official ID H-0790-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Fibroid Bully 16 oz and 32 oz recall — LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

Company / brand: LIQUID BLENZ recalls

Official ID H-0789-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Menopause Bully 16 oz and 32 oz recall — LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

Company / brand: LIQUID BLENZ recalls

Official ID H-0788-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Immunity Enhancer Elderberry 16 oz and 32 oz recall — LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

Company / brand: LIQUID BLENZ recalls

Official ID H-0787-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Pure Libido Drink 16 oz and 32 oz recall — LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

Company / brand: LIQUID BLENZ recalls

Official ID H-0786-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Pure Diabetes Bully 16 oz and 32 oz recall — LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

Company / brand: LIQUID BLENZ recalls

Official ID H-0785-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Sea Moss Tonic 16 oz and 32 recall — LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

Company / brand: LIQUID BLENZ recalls

Official ID H-0784-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Blackseed Bitters 16 oz and 32 oz recall — LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

Company / brand: LIQUID BLENZ recalls

Official ID H-0783-2026 · Official record ↗

FDA Class II · Food · May 27, 2026

Liquid Blenz Soursop Bitters 16 oz and 32 oz recall — LIQUID BLENZ CORP

May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

Company / brand: LIQUID BLENZ recalls

Official ID H-0782-2026 · Official record ↗

FDA Class I · Drug · May 27, 2026

MG217 Multi-Symptom Treatment Cream & Skin Protectant (colloidal oatmeal 2%) recall — Wisconsin Pharmacal Company

Microbial Contamination of Non-Sterile Products: confirmed presence of Staphylococcus Aureus.

Company / brand: Wisconsin Pharmacal Company recalls

Official ID D-0553-2026 · Official record ↗

FDA Class II · Drug · May 27, 2026

Vitamin B-Complex recall — Safecor Health, LLC

Presence of a Foreign Substance; black particles observed in liquid

Company / brand: Safecor Health recalls

Official ID D-0549-2026 · Official record ↗

FDA Class II · Drug · May 27, 2026

fentaNYL Citrate recall — IntegraDose Compounding Services LLC

Subpotent Drug

Company / brand: IntegraDose Compounding Services recalls

Official ID D-0548-2026 · Official record ↗

FDA Class II · Drug · May 27, 2026

cimzia (certolizumab pegol) recall — UCB Biosciences Inc.

Lack of Assurance of Sterility

Company / brand: UCB Biosciences recalls

Official ID D-0546-2026 · Official record ↗

FDA Class II · Drug · May 27, 2026

Erythromycin Tablets recall — Zydus Pharmaceuticals (USA) Inc

CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit

Company / brand: Zydus Pharmaceuticals (USA) recalls

Official ID D-0545-2026 · Official record ↗

FDA Class II · Drug · May 27, 2026

Erythromycin Tablets recall — Zydus Pharmaceuticals (USA) Inc

CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit

Company / brand: Zydus Pharmaceuticals (USA) recalls

Official ID D-0544-2026 · Official record ↗

FDA Class II · Drug · May 27, 2026

Estradiol Gel recall — ANI Pharmaceuticals, Inc.

Defective Container; packets were found to be either empty or partially full.

Company / brand: ANI Pharmaceuticals recalls

Official ID D-0543-2026 · Official record ↗

FDA Class II · Drug · May 27, 2026

Gas-X recall — Haleon US Holdings LLC

Labeling: Not Elsewhere Classified- Incomplete inactive ingredient information on the carton labeling.

Company / brand: Haleon US Holdings recalls

Official ID D-0542-2026 · Official record ↗

FDA Class II · Drug · May 27, 2026

Liraglutide Injection recall — Lupin Pharmaceuticals Inc.

Presence of particulate matter: a white thread-like structure in the cartridge

Company / brand: Lupin Pharmaceuticals recalls

Official ID D-0541-2026 · Official record ↗

FDA Class III · Drug · May 27, 2026

Busulfan Injection recall — Sagent Pharmaceuticals

Failed Impurities/Degradation Specifications

Company / brand: Sagent Pharmaceuticals recalls

Official ID D-0539-2026 · Official record ↗

FDA Class II · Drug · May 27, 2026

Atomoxetine Capsules HCL recall — Safecor Health, LLC

Labeling: Label Mix-Up: Atomoxetine HCl 25mg Capsule incorrectly labeled as Atomoxetine HCl 10mg Capsule.

Company / brand: Safecor Health recalls

Official ID D-0538-2026 · Official record ↗

FDA Class III · Drug · May 27, 2026

Primidone Tablets recall — Amerisource Health Services LLC

Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

Company / brand: Amerisource Health Services recalls

Official ID D-0537-2026 · Official record ↗

FDA Class III · Drug · May 27, 2026

Primidone Tablets recall — Amerisource Health Services LLC

Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

Company / brand: Amerisource Health Services recalls

Official ID D-0536-2026 · Official record ↗

FDA Class III · Drug · May 27, 2026

Primidone Tablets recall — Golden State Medical Supply Inc.

Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

Company / brand: Golden State Medical Supply recalls

Official ID D-0535-2026 · Official record ↗

FDA Class III · Drug · May 27, 2026

Primidone Tablets recall — Golden State Medical Supply Inc.

Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

Company / brand: Golden State Medical Supply recalls

Official ID D-0534-2026 · Official record ↗

FDA Class III · Drug · May 27, 2026

Primidone Tablets USP recall — Lannett Company Inc.

Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

Company / brand: Lannett Company recalls

Official ID D-0533-2026 · Official record ↗

NHTSA · Vehicle · May 26, 2026

Tiffin Motorhomes Fuel System, Diesel recall (26V338000)

A fuel leak in the presence of an ignition source, increases the risk of a fire.

Company / brand: Tiffin Motorhomes recalls

Official ID 26V338000 · Official record ↗

NHTSA · Vehicle · May 26, 2026

Alliance RV Paradigm recall (26V337000)

Broken shock retainer bolt heads and washers may detach and become a road hazard to other vehicles, increasing the risk of a crash.

Company / brand: Alliance RV recalls

Official ID 26V337000 · Official record ↗

NHTSA · Vehicle · May 26, 2026

Forest River Suspension recall (26V336000)

Broken shock retainer bolt heads and washers may detach and become a road hazard for other vehicles, increasing the risk of a crash.

Company / brand: Forest River recalls

Official ID 26V336000 · Official record ↗

NHTSA · Vehicle · May 26, 2026

Ford Motor Company Equipment recall (26V335000)

The incorrect tire size, tire pressures, and GAWR listed on the labels can allow the vehicle to be overloaded or have improperly inflated tires, increasing the risk of a crash.

Company / brand: Ford Motor Company recalls

Official ID 26V335000 · Official record ↗

NHTSA · Vehicle · May 22, 2026

Brinkley RV Model Z recall (26V334000)

Broken shock retainer bolt heads and washers may detach and become a road hazard for other vehicles, increasing the risk of a crash.

Company / brand: Brinkley RV recalls

Official ID 26V334000 · Official record ↗

NHTSA · Vehicle · May 22, 2026

Coach And Equipment MFG Equipment Adaptive/Mobility recall (26V333000)

An unsecured wheelchair can move during transit, increasing the risk of injury.

Company / brand: Coach And Equipment MFG recalls

Official ID 26V333000 · Official record ↗

NHTSA · Vehicle · May 21, 2026

Honda Air Bags recall (26V332000)

Air bags that deploy unintentionally during a crash increase the risk of injury.

Company / brand: Honda recalls

Official ID 26V332000 · Official record ↗

NHTSA · Vehicle · May 21, 2026

Nissan Kicks recall (26V331000)

A partial or blank screen display will not show critical safety information such as vehicle speed and warning lights, increasing the risk of a crash.

Company / brand: Nissan North America recalls

Official ID 26V331000 · Official record ↗

NHTSA · Vehicle · May 21, 2026

Bentley Motors Power Train recall (26V330000)

A loose hub securing nut can cause vibration and a loss of steering control, increasing the risk of a crash.

Company / brand: Bentley Motors recalls

Official ID 26V330000 · Official record ↗

NHTSA · Vehicle · May 21, 2026

General Motors Air Bags recall (26V329000)

An inflator rupture may result in sharp metal fragments striking the driver or other occupants, resulting in serious injury or death.

Company / brand: General Motors recalls

Official ID 26V329000 · Official record ↗

NHTSA · Vehicle · May 21, 2026

Chrysler Air Bags recall (26V328000)

Delayed air bag deployment during a crash increases the risk of injury.

Company / brand: Chrysler recalls

Official ID 26V328000 · Official record ↗

NHTSA · Vehicle · May 21, 2026

Chrysler Back Over Prevention recall (26V327000)

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 26V327000 · Official record ↗

NHTSA · Vehicle · May 21, 2026

Chrysler Back Over Prevention recall (26V326000)

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 26V326000 · Official record ↗

NHTSA · Vehicle · May 21, 2026

General Motors Air Bags recall (26V325000)

A detached end cap or inflator rupture can allow compressed gas to escape and project the end cap or fragments of the inflator into the vehicle, increasing the risk of injury.

Company / brand: General Motors recalls

Official ID 26V325000 · Official record ↗

CPSC · Consumer Product · May 21, 2026

Bethlehem Lights Recalls Bethlehem Lights 10-inch Illuminated Ribbon Spheres Due to Risk of Serious Injury or Death from Fire Hazard; Sold by QVC

The LED lights on the recalled illuminated spheres can overheat, posing a risk of serious injury or death from a fire hazard.

Company / brand: Bethlehem Lights recalls

Official ID 26504 · Official notice ↗

CPSC · Consumer Product · May 21, 2026

ABC Trading Recalls WSDZ Light-up Glasses Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Button Cell Batteries

The recalled glasses violate the mandatory standard for consumer products with button cell and coin batteries because the button cell batteries can be accessed easily by children, …

Company / brand: ABC Trading recalls

Official ID 26503 · Official notice ↗

CPSC · Consumer Product · May 21, 2026

PandaEar Recalls Portable Hook-On Chairs Due to Risk of Serious Injury or Death from Fall Hazard; Violates Mandatory Standard for Portable Hook-On Chairs

The recalled portable hook-on chairs violate the mandatory standard for portable hook-on chairs because the crotch restraints can be removed without the use of a tool and infants c…

Company / brand: PandaEar of Lake Dallas recalls

Official ID 26502 · Official notice ↗

CPSC · Consumer Product · May 21, 2026

Lil Pick Up Recalls Youth All-Terrain Vehicles (ATVs) Due to Risk of Serious Injury or Death from Crash and Burn Hazards; Violates Mandatory Standard for ATVs

The recalled youth ATVs violate the federal mandatory ATV safety standard, posing a risk of serious injury or death. The youth ATVs fail to meet mechanical suspension requirements,…

Company / brand: Lil Pick Up recalls

Official ID 26501 · Official notice ↗

CPSC · Consumer Product · May 21, 2026

Orb Funkee Squeeze Toys Recalled Due to Risk of Serious Injury or Death from Asbestos Exposure; Imported by The Orb Factory

The recalled Orb Funkee squeeze toys may contain fibrous tremolite (asbestos) in the sand, which can cause adverse health issues if inhaled.

Company / brand: The Orb Factory recalls

Official ID 26499 · Official notice ↗

CPSC · Consumer Product · May 21, 2026

Resistance Bands Recalled Due to Serious Injury from Impact Hazard; Imported by HomeProGym

The recalled resistance bands can forcefully separate from the handle during use, posing a risk of serious injury from impact hazard.

Company / brand: Supa Products Pte recalls

Official ID 26498 · Official notice ↗

CPSC · Consumer Product · May 21, 2026

ABC Trading Recalls Children's Toys Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys

The recalled children's toys violate the mandatory standard for toys because they contain button cell batteries and the compartments that hold the batteries can be easily accessed …

Company / brand: ABC Trading recalls

Official ID 26497 · Official notice ↗

NHTSA · Vehicle · May 20, 2026

Alliance RV Equipment recall (26V324000)

The heating pad may overheat in the battery compartment, increasing the risk of a fire.

Company / brand: Alliance RV recalls

Official ID 26V324000 · Official record ↗

NHTSA · Vehicle · May 20, 2026

Wabash National Exterior Lighting recall (26V323000)

Missing conspicuity tape can reduce the visibility of the trailer to other drivers, increasing the risk of a crash.

Company / brand: Wabash National recalls

Official ID 26V323000 · Official record ↗

NHTSA · Vehicle · May 20, 2026

KZRV Durango recall (26V322000)

Broken shock retainer bolt heads and washers may detach and become a road hazard for other vehicles, increasing the risk of a crash.

Company / brand: K.Z recalls

Official ID 26V322000 · Official record ↗

NHTSA · Vehicle · May 20, 2026

Volkswagen Tiguan recall (26V321000)

A rearview camera that does not display an image can reduce the driver's rear view, increasing the risk of a crash.

Company / brand: Volkswagen Group recalls

Official ID 26V321000 · Official record ↗

NHTSA · Vehicle · May 20, 2026

Toyota Tundra recall (26V320000)

A loss of drive power increases the risk of a crash.

Company / brand: Toyota Motor Engineering & Manufacturing recalls

Official ID 26V320000 · Official record ↗

NHTSA · Vehicle · May 20, 2026

Blue Bird Vision School Bus recall (26V319000)

An unsecured wheelchair can move during transit, increasing the risk of injury.

Company / brand: Blue Bird Body Company recalls

Official ID 26V319000 · Official record ↗

NHTSA · Vehicle · May 20, 2026

Turtle Top Equipment Adaptive/Mobility recall (26V318000)

An unsecured wheelchair can move during transit, increasing the risk of injury.

Company / brand: Turtle Top recalls

Official ID 26V318000 · Official record ↗

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Government sources last checked October 22, 2026 at 12:00 PM UTC.