Fresh Recalls

Latest recalls — page 21

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

3,525 recalls in our current data. Showing 2,001–2,100, newest first.

FDA Class I · Food · July 1, 2026

1 recall — Utz Quality Foods, LLC

Potential presence of Salmonella.

Company / brand: Utz Quality Foods recalls

Official ID H-1112-2026 · Official record ↗

FDA Class III · Food · July 1, 2026

Roast beef and cheddar closed face sandwich packed in clear plastic wrap with a green adhe recall — Produce Innovations

Incorrect Product Label; Roast Beef and Swiss closed face sub sandwich labeled as Turkey and Cheddar closed face sub sandwich

Company / brand: Produce Innovations recalls

Official ID H-1111-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

El David Gelee recall — Alb-USA Enterprises Inc

Undeclared colors (FD&C Yellow 5 and FD&C Red 40).

Company / brand: Alb-USA Enterprises recalls

Official ID H-1110-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

Spring & Mulberry Blood Orange Date-Sweetened Chocolate recall — Spring & Mulberry Inc.

Potential Salmonella contamination

Company / brand: Spring & Mulberry recalls

Official ID H-1106-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

Spring & Mulberry Coffee Date-Sweetened Chocolate recall — Spring & Mulberry Inc.

Potential Salmonella contamination

Company / brand: Spring & Mulberry recalls

Official ID H-1105-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

Spring & Mulberry Sea Salt Date-Sweetened Chocolate recall — Spring & Mulberry Inc.

Potential Salmonella contamination

Company / brand: Spring & Mulberry recalls

Official ID H-1104-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

1) Spring & Mulberry Pure Dark Date-Sweetened Chocolate recall — Spring & Mulberry Inc.

Potential Salmonella contamination

Company / brand: Spring & Mulberry recalls

Official ID H-1103-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

Spring & Mulberry Pecan Date Date-Sweetened Chocolate recall — Spring & Mulberry Inc.

Potential Salmonella contamination.

Company / brand: Spring & Mulberry recalls

Official ID H-1102-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

Spring & Mulberry Mulberry Fennel Date-Sweetened Chocolate recall — Spring & Mulberry Inc.

Potential Salmonella contamination.

Company / brand: Spring & Mulberry recalls

Official ID H-1101-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

Spring & Mulberry Mango Chili Date-Sweetened Chocolate recall — Spring & Mulberry Inc.

Potential Salmonella contamination

Company / brand: Spring & Mulberry recalls

Official ID H-1100-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

Spring & Mulberry Lavender Rose Date-Sweetened Chocolate recall — Spring & Mulberry Inc.

Potential Salmonella contamination

Company / brand: Spring & Mulberry recalls

Official ID H-1099-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

Spring & Mulberry Earl Grey Date-Sweetened Chocolate recall — Spring & Mulberry Inc.

Potential Salmonella contamination

Company / brand: Spring & Mulberry recalls

Official ID H-1098-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

Spring & Mulberry Mixed Berry Date-Sweetened Chocolate recall — Spring & Mulberry Inc.

Potential Salmonella contamination

Company / brand: Spring & Mulberry recalls

Official ID H-1097-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

Spring & Mulberry Mint Leaf Date-Sweetened Chocolate recall — Spring & Mulberry Inc.

Potential Salmonella contamination

Company / brand: Spring & Mulberry recalls

Official ID H-1096-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Motor City Pizza Co recall — Champion Foods, LLC

potential salmonella contamination

Company / brand: Champion Foods recalls

Official ID H-1095-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Saffron Cardamon Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1094-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Orange Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1093-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Peach Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1092-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Mint Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1091-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Masala Chaash Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1090-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Plain Chaash Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1089-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Mango-Pina-Orange Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1088-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Mango-Pina-Strawberry Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1087-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Strawberry Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1086-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Pineapple Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1085-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Salty Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1084-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Sweet Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1083-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Rose Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1082-2026 · Official record ↗

FDA Class II · Food · July 1, 2026

Joy Mango Lassi 16 oz recall — Joy Gourmet Foods LLC.

Product not adequately pasteurized

Company / brand: Joy Gourmet Foods recalls

Official ID H-1081-2026 · Official record ↗

FDA Class I · Food · July 1, 2026

Dried Herring Fish 7 oz recall — Prime Food Processing LLC.

Improperly eviscerated which may result in Clostridium botulinum contamination

Company / brand: Prime Food Processing recalls

Official ID H-1080-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

Perampanel CIII Tablets recall — SUN PHARMACEUTICAL INDUSTRIES INC

Labeling: Label Mix-up: 10mg Perampanel CIII tablet was found in a Perampanel CIII bottle labeled Perampanel 6 mg tablets.

Company / brand: SUN PHARMACEUTICAL INDUSTRIES recalls

Official ID D-0628-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

Povi-One recall — Elevate Oral Care

sub potency

Company / brand: Elevate Oral Care recalls

Official ID D-0627-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

Lacosamide Tablets recall — Annora Pharma Private Limited

Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg tablet in a bottle of Lacosamide Tablets USP, 100mg.

Company / brand: Annora Pharma Private recalls

Official ID D-0626-2026 · Official record ↗

FDA Class I · Drug · July 1, 2026

BD ChloraPrep FREPP Clear recall — CareFusion 213, LLC

Non-Sterility: Due to presence of Aspergillus penicillioides. And Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.

Company / brand: CareFusion 213 recalls

Official ID D-0625-2026 · Official record ↗

FDA Class I · Drug · July 1, 2026

BD ChloraPrep Clear (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (I recall — CareFusion 213, LLC

Non-Sterility: Due to presence of Aspergillus penicillioides.

Company / brand: CareFusion 213 recalls

Official ID D-0624-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

BD ChloraPrep FREPP Clear recall — CareFusion 213, LLC

Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.

Company / brand: CareFusion 213 recalls

Official ID D-0623-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

BD ChloraPrep Clear recall — CareFusion 213, LLC

Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.

Company / brand: CareFusion 213 recalls

Official ID D-0622-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

PReye Vitamin See Antioxidant Preservative Free Eye Drops recall — PReye LLC

Lack of Assurance of Sterility

Company / brand: PReye recalls

Official ID D-0621-2026 · Official record ↗

FDA Class III · Drug · July 1, 2026

hydrOXYzine Hydrochloride Oral Solution recall — ANI Pharmaceuticals, Inc.

Presence of foreign substance

Company / brand: ANI Pharmaceuticals recalls

Official ID D-0619-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag recall — Central Admixture Pharmacy Services, Inc.

Incorrect product formulation: bag did not contain copper and famotidine per label.

Company / brand: Central Admixture Pharmacy Services recalls

Official ID D-0618-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

DULOXETINE D/R recall — Direct Rx

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit

Company / brand: Direct Rx recalls

Official ID D-0617-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

Sensipar (cinacalcet) Tablets recall — Amgen, Inc.

CGMP Deviations

Company / brand: Amgen recalls

Official ID D-0616-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

Corlanor (ivabradine) tablets recall — Amgen, Inc.

Presence of Foreign Substance.

Company / brand: Amgen recalls

Official ID D-0615-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

Sensipar (cinacalcet) Tablets recall — Amgen, Inc.

CGMP Deviations

Company / brand: Amgen recalls

Official ID D-0614-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

Sensipar (cinacalcet) Tablets recall — Amgen, Inc.

CGMP Deviations

Company / brand: Amgen recalls

Official ID D-0613-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

Corlanor (ivabradine) tablets recall — Amgen, Inc.

Presence of Foreign Substance.

Company / brand: Amgen recalls

Official ID D-0612-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

Fenofibrate Capsules recall — Ajanta Pharma USA Inc

CGMP Deviations

Company / brand: Ajanta Pharma USA recalls

Official ID D-0611-2026 · Official record ↗

FDA Class II · Drug · July 1, 2026

Carton Label recall — The Harvard Drug Group LLC

Subpotent Drug

Company / brand: The Harvard Drug Group recalls

Official ID D-0609-2026 · Official record ↗

NHTSA · Vehicle · June 30, 2026

Teko Back Over Prevention recall (26V420000)

A vehicle that does not make a sound may fail to alert pedestrians of an approaching vehicle, increasing the risk of a crash or injury.

Company / brand: Teko recalls

Official ID 26V420000 · Official record ↗

NHTSA · Vehicle · June 30, 2026

Nissan Rogue recall (26V419000)

A missing gear selection indicator may lead to unintended vehicle movement or a vehicle rollaway, increasing the risk of a crash.

Company / brand: Nissan North America recalls

Official ID 26V419000 · Official record ↗

NHTSA · Vehicle · June 30, 2026

Ford Motor Company Visibility recall (26V418000)

Windshield wipers or a washing system that fails to function as intended can reduce visibility, increasing the risk of a crash.

Company / brand: Ford Motor Company recalls

Official ID 26V418000 · Official record ↗

NHTSA · Vehicle · June 30, 2026

Ford Mustang Mach E recall (26V417000)

Differential pinion shaft fracture may result in a loss of drive power, or unintended vehicle movement if the vehicle is in park without the parking brake applied, increasing the r…

Company / brand: Ford Motor Company recalls

Official ID 26V417000 · Official record ↗

NHTSA · Vehicle · June 30, 2026

Jayco Equipment recall (26V416000)

A dinette that moves during transit may increase the risk of injury.

Company / brand: Jayco recalls

Official ID 26V416000 · Official record ↗

NHTSA · Vehicle · June 30, 2026

Ford Motor Company Back Over Prevention recall (26V415000)

A vehicle that does not produce a warning sound may fail to alert pedestrians of an approaching vehicle, increasing the risk of injury.

Company / brand: Ford Motor Company recalls

Official ID 26V415000 · Official record ↗

NHTSA · Vehicle · June 30, 2026

Chrysler Electronic Stability Control (Esc) recall (26V414000)

A loss of electronic stability control and/or electronic brake assist increases the risk of a crash.

Company / brand: Chrysler recalls

Official ID 26V414000 · Official record ↗

NHTSA · Vehicle · June 30, 2026

Chrysler Power Train recall (26V413000)

A missing gear selection indicator may lead to unintended vehicle movement or a vehicle rollaway, increasing the risk of a crash.

Company / brand: Chrysler recalls

Official ID 26V413000 · Official record ↗

NHTSA · Vehicle equipment · June 30, 2026

Nissan North America Power Train recall (26E039000)

An instrument panel display that does not show critical information, such as gear selection, increases the risk of a crash.

Company / brand: Nissan North America recalls

Official ID 26E039000 · Official record ↗

NHTSA · Vehicle · June 29, 2026

Tiffin Motorhomes Equipment recall (26V412000)

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

Company / brand: Tiffin Motorhomes recalls

Official ID 26V412000 · Official record ↗

NHTSA · Vehicle · June 29, 2026

Jayco Equipment recall (26V411000)

Referencing incorrect weight information may lead to unintentionally overloading the vehicle, increasing the risk of a crash.

Company / brand: Jayco recalls

Official ID 26V411000 · Official record ↗

NHTSA · Vehicle · June 26, 2026

Nissan Sentra recall (26V410000)

An unexpected loss of drive power can increase the risk of a crash. In addition, a driveshaft that is not fully engaged can result in a vehicle rollaway if the parking brake is not…

Company / brand: Nissan North America recalls

Official ID 26V410000 · Official record ↗

NHTSA · Vehicle · June 26, 2026

Altec Digger Derrick recall (26V409000)

While using the pole rack at full capacity, an incorrect high vertical center of gravity during braking and cornering may lead to a loss of vehicle control, increasing the risk of …

Company / brand: Altec Industries recalls

Official ID 26V409000 · Official record ↗

NHTSA · Vehicle · June 26, 2026

Thomas Built Buses Saf-T-Liner HDX2 recall (26V408000)

A door that fails to open or close increases the risk of injury to occupants in a crash.

Company / brand: Daimler Trucks North America recalls

Official ID 26V408000 · Official record ↗

NHTSA · Vehicle · June 26, 2026

Thomas Built Buses Saf-T-Liner HDX2 recall (26V407000)

A door that fails to open or close increases the risk of injury to occupants in a crash.

Company / brand: Daimler Trucks North America recalls

Official ID 26V407000 · Official record ↗

NHTSA · Vehicle · June 26, 2026

Diamond Coach Vip recall (26V406000)

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

Company / brand: Diamond Coach recalls

Official ID 26V406000 · Official record ↗

CPSC · Consumer Product · June 25, 2026

Combination Smoke and Carbon Monoxide (CO) Detectors Recalled Due to Risk of Serious Injury or Death from Failure to Alert Consumers to Fire; Sold Exclusively on Amazon.com by Treatlife Technology

The recalled detectors can fail to alert consumers of a fire, posing a risk of serious injury or death from smoke inhalation or burns.

Company / brand: Treatlife Technology Co recalls

Official ID 26582 · Official notice ↗

CPSC · Consumer Product · June 25, 2026

Daikin Comfort Technologies Manufacturing Recalls Amana Air Conditioners and Heat Pumps Due to Risk of Serious Injury from Fire and Burns

The heating element can remain energized during a ground fault, despite being turned off, posing a risk of fire or burn injury to consumers.

Company / brand: Daikin Comfort Technologies Manufacturing recalls

Official ID 26581 · Official notice ↗

CPSC · Consumer Product · June 25, 2026

Honlyne LED Party Favors Recalled Due to Risk of Serious Injury Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Button Cell Batteries; Sold by Huizhou Rongheng Network Technology

The LED party favors violate the mandatory safety standard for consumer products because the battery compartment within the light-up products contains button cell batteries that ca…

Company / brand: ABGA Advanced Trading Co recalls

Official ID 26580 · Official notice ↗

CPSC · Consumer Product · June 25, 2026

Montessori Busy Board Toys Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by Small Fish

The busy boards violate the mandatory safety standard for toys because magnets can detach, posing a deadly ingestion hazard. When high-powered magnets are swallowed, the ingested m…

Company / brand: Lesonic Technology Co recalls

Official ID 26579 · Official notice ↗

CPSC · Consumer Product · June 25, 2026

Raychy Children's Light Sneakers Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Coin Batteries; Imported by Carina and Rambo

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

Company / brand: Shenzhen Qicheng Trading Co recalls

Official ID 26578 · Official notice ↗

CPSC · Consumer Product · June 25, 2026

Shield Line Recalls MedPride Baby Oil Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging

The baby oil contains low-viscosity hydrocarbons, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The baby oil's packaging is not ch…

Company / brand: Shield Line recalls

Official ID 26577 · Official notice ↗

CPSC · Consumer Product · June 25, 2026

Southern Telecom Expands Recall of Lomi Waxing Kits Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Additional Model and Reported Incidents

The roll-on warmers' power cord can overheat and short circuit, posing a risk of serious injury or death from fire, burn and electrical shock hazards.

Company / brand: Southern Telecom recalls

Official ID 26576 · Official notice ↗

CPSC · Consumer Product · June 25, 2026

Super Off-Road Solar Power Banks Recalled Due to Overheating; Imported by Spector & Co.

The solar power bank's lithium-ion battery can swell and overheat, posing a burn hazard to consumers.

Company / brand: Spector & Co recalls

Official ID 26575 · Official notice ↗

CPSC · Consumer Product · June 25, 2026

Yamazuki Recalls Youth All-Terrain Vehicles (ATVs) Due to Risk of Serious Injury or Death from Crash; Violate Mandatory Standard for ATVs

The recalled youth ATVs violate the mandatory safety standard for ATVs because they are missing brake lights, reducing visibility of the youth ATV to other vehicles, posing a deadl…

Company / brand: Yongkang Ruihe Metal Products Co recalls

Official ID 26574 · Official notice ↗

CPSC · Consumer Product · June 25, 2026

Kith Retail Recalls Children's Loungewear Sets Due to Risk of Serious Injury from Burn Hazard; Violate Mandatory Standards for Children's Sleepwear

The recalled children's loungewear sets violate the mandatory flammability standards for children's sleepwear, posing a risk of serious burn injuries.

Company / brand: Kith Retail of Brooklyn recalls

Official ID 26507 · Official notice ↗

NHTSA · Vehicle · June 24, 2026

Harbinger Motors Stripped Chassis recall (26V405000)

Broken or loose steering gear bolts can cause a loss of steering control, increasing the risk of a crash.

Company / brand: Harbinger Motors recalls

Official ID 26V405000 · Official record ↗

NHTSA · Vehicle · June 24, 2026

Elgin Pelican recall (26V404000)

The defective batteries may overheat, increasing the risk of a fire.

Company / brand: Elgin Sweeper Company recalls

Official ID 26V404000 · Official record ↗

NHTSA · Vehicle · June 24, 2026

Ford Bronco recall (26V403000)

A detached fender flare can become a road hazard and increase the risk of a crash.

Company / brand: Ford Motor Company recalls

Official ID 26V403000 · Official record ↗

NHTSA · Vehicle · June 24, 2026

Ford Motor Company Power Train recall (26V402000)

Park system damage may result in a vehicle rollaway, increasing the risk of a crash.

Company / brand: Ford Motor Company recalls

Official ID 26V402000 · Official record ↗

NHTSA · Vehicle · June 24, 2026

Airstream Electrical System recall (26V401000)

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

Company / brand: Airstream recalls

Official ID 26V401000 · Official record ↗

NHTSA · Vehicle · June 24, 2026

Hyundai Motor America Electrical System recall (26V400000)

An instrument panel display that fails to show critical safety information, such as the speedometer or warning lights, increases the risk of a crash.

Company / brand: Hyundai Motor America recalls

Official ID 26V400000 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Brand Name recall — Thoratec LLC

Due to 11 volt Backup Battery failures.

Company / brand: Thoratec recalls

Official ID Z-2520-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Brand Name recall — Thoratec LLC

Due to 11 volt Backup Battery failures.

Company / brand: Thoratec recalls

Official ID Z-2519-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Brand Name recall — Thoratec LLC

Due to 11 volt Backup Battery failures.

Company / brand: Thoratec recalls

Official ID Z-2518-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Splashwire Hydrophilic Guide Wire recall — Merit Medical Systems, Inc.

Due to unsealed portions of pouches.

Company / brand: Merit Medical Systems recalls

Official ID Z-2517-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Brand Name recall — Inspire Medical Systems Inc.

Products are labeled with incorrect Use By Date, extending beyond the validated three-year shelf life from date of manufacturer. Material degradation of a product past its Use By D…

Company / brand: Inspire Medical Systems recalls

Official ID Z-2516-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Brand Name recall — Inspire Medical Systems Inc.

Products are labeled with incorrect Use By Date, extending beyond the validated three-year shelf life from date of manufacturer. Material degradation of a product past its Use By D…

Company / brand: Inspire Medical Systems recalls

Official ID Z-2515-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code recall — BD SWITZERLAND SARL

Due to stopcock issues when using the plastic luer-lok syringe, the connection at the Port C may over thread or continue to spin rather than tightening securely. This behavior has …

Company / brand: BD SWITZERLAND SARL recalls

Official ID Z-2514-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

iLet Bionic Pancreas recall — Beta Bionics, Inc.

The reason for the recall is: it was found in version 3.3.6 of the iLet ACE Pump firmware and all previous releases that a screen unlock failure could occur when the user successfu…

Company / brand: Beta Bionics recalls

Official ID Z-2513-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Product Name recall — Staar Surgical AG

Due to a software coding issues for calculating the implant orientation diagram printout for the implantation for toric implantable collamer lenses.

Company / brand: Staar Surgical AG recalls

Official ID Z-2509-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2508-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2507-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2506-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as CLOVIS HYSTEROSCOPY recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2505-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2504-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as BASIC GYN recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2503-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2502-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2501-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2500-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2499-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

MEDLINE Medical Procedure Kits labeled as recall — Medline Industries, LP

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…

Company / brand: Medline Industries recalls

Official ID Z-2498-2026 · Official record ↗

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