The Recall Desk

Archive

October 2025 recalls

804 recalls were announced in October 2025.

What the numbers show

Critical
179
Severe
78
High
390
Moderate
154
Low
3

Of the 804 recalls this month scored against our rubric, 22% are Critical, 10% are Severe.

1–100 of 804

  • SevereNHTSA·25V748000·2025-10-31

    BMW Recalls 2000-2001 X5 Vehicles Due to Air Bag Inflator Defect

    BMW is recalling 2000-2001 X5 vehicles because the driver's air bag inflator may explode during deployment, posing a risk of serious injury or death.

    Product
    BMW — BMW X5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V750000·2025-10-31

    Par Nado Alto Travel Trailers Recalled for Gas Leak Risk

    Par Nado is recalling 2019-2020 Alto travel trailers because aluminum burner tubes may crack, causing a gas leak that could lead to fire.

    Product
    SAFARI CONDO — SAFARI CONDO ALTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V749000·2025-10-31

    Heil Recalls Side Loader Garbage Trucks Due to Fuel Leak Risk

    Heil is recalling 2023-2025 side loader garbage trucks with specific CNG fuel systems because manual cylinder valves may crack and leak natural gas, increasing fire risk.

    Product
    HEIL — HEIL SIDE LOADER GARBAGE TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V752000·2025-10-31

    Micro Bird Recalls Transit Buses With Defective Wheelchair Restraints

    Micro Bird is recalling 2024-2026 G5 and 2025 T-Series transit buses because wheelchair restraints may fail to lock, increasing injury risk.

    Product
    MICRO BIRD — MICRO BIRD G5 TRANSIT BUS, T-SERIES TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V751000·2025-10-31

    Micro Bird Recalls School Buses With Defective Wheelchair Restraints

    Micro Bird is recalling 2023-2026 G5 and 2025 T-Series school buses because wheelchair restraints may fail to lock, increasing injury risk.

    Product
    MICRO BIRD — MICRO BIRD T-SERIES SCHOOL BUS, G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26058·2025-10-30

    Kayak paddles recalled after 80 reports of breaking during use

    About 700 Werner Stealth and Covert kayak paddles are being recalled after 80 reports of the paddles breaking during use, posing a drowning hazard.

    Product
    Stealth and Covert Kayak Paddles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26054·2025-10-30

    Off-road vehicles recalled over alternator cable that can short and ignite

    About 5,130 Polaris Ranger XP 1000 NorthStar off-road vehicles are being recalled because an improperly routed alternator cable can short against the battery; six incidents include one fire.

    Product
    Model Year 2025-2026 Ranger XP 1000 NorthStar and Ranger Crew XP 1000 NorthStar Recreational Off-Road Vehicles (ROVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26064·2025-10-30

    Chainsaws recalled because the chain brake may not activate

    About 90,860 Milwaukee Tool M18 FUEL top handle chainsaws are being recalled because the chain brake may not activate; two reports include one lacerated finger.

    Product
    Milwaukee Tool M18 FUELTM Top Handle Chainsaw with either a 12" or 14" bar
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V743000·2025-10-30

    Jayco Recalls 2025-2026 Entegra Recreational Vehicles for Slide-Out Defect

    Jayco is recalling 2025-2026 Entegra recreational vehicles because slide-out rooms can deploy while the vehicle is moving, increasing crash risk.

    Product
    ENTEGRA — ENTEGRA CORNERSTONE, ANTHEM, ASPIRE, CORNERSTONE RESERVE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V742000·2025-10-30

    Smeal Recalls 2024-2026 Aerial Vehicles Due to Hydraulic Hose Defect

    Smeal Holding, LLC is recalling 29 emergency response vehicles because a defective crimp may cause hydraulic hoses to leak, risking injury or fire.

    Product
    SMEAL — SMEAL REAR MOUNT AERIAL, AERIAL, MID MOUNT AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E071000·2025-10-30

    Honda Recalls 18-Inch Aluminum Alloy Wheels for Civic Vehicles

    Honda is recalling 18-inch aluminum alloy wheels for 2016-2021 Civic vehicles because a manufacturing error may allow them to detach, increasing crash risk.

    Product
    WHEELS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V741000·2025-10-30

    Jeep Wrangler and Grand Cherokee 4Xe vehicles fire risk battery recall

    Chrysler is recalling certain 2020–2025 Jeep Wrangler 4Xe and 2022–2026 Grand Cherokee 4Xe vehicles because the high voltage battery may fail internally and cause a vehicle fire while parked or driving.

    Product
    JEEP — JEEP GRAND CHEROKEE, WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26051·2025-10-30

    Bicycle lights recalled after five battery fires or explosions reported

    About 3,790 Knog Blinder 900 and Blinder 1300 front bicycle lights are being recalled after five reports of the lithium-ion battery catching fire or exploding.

    Product
    Knog Blinder 900 and Blinder 1300 Front Bicycle Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26059·2025-10-30

    Dining chairs recalled after 149 reports of chair legs breaking

    About 54,930 Crate & Barrel Ana Dining Chairs are being recalled after 149 reports of chair legs breaking, including 10 reports of injuries to the head, back, arms and face.

    Product
    Ana Dining Chair
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26052·2025-10-30

    Play yard mattresses recalled over poor fit and suffocation entrapment hazard

    About 15,000 Modera Pack N Play play yard mattresses are being recalled because they may not fit certain play yards, creating gaps that pose a deadly entrapment hazard.

    Product
    Organic Cotton Pack N Play Mattress Dual-Sided Portable Baby Crib Pad
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V745000·2025-10-30

    2025 Kia Telluride and 2026 Sorento Spare Tire Assembly Recall

    Kia is recalling certain 2025 Telluride and 2026 Sorento vehicles due to an incorrect spare tire that can impair the anti-lock braking and traction control systems, increasing crash risk.

    Product
    KIA — KIA TELLURIDE, SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V740000·2025-10-30

    KTM and Husqvarna Recall 2024 Motorcycles for Fuel Cap Seal Defect

    KTM North America is recalling 5,488 2024 KTM and Husqvarna motorcycles because the fuel filler cap seal may crack and leak fuel, increasing the risk of fire or injury.

    Product
    KTM — KTM, HUSQVARNA 990 DUKE, 390 DUKE, SVARTPILEN 401, 250 DUKE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V747000·2025-10-30

    Remote Vans Recalls 2025 Aegis and Oasis Motorhomes for Weight Rating Issues

    Remote Vans is recalling 2025 Aegis and Oasis motorhomes because optional equipment may cause the vehicles to exceed their Gross Vehicle Weight Rating, increasing crash risk.

    Product
    REMOTE VANS — REMOTE VANS AEGIS, OASIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26061·2025-10-30

    Convertible high chairs recalled for missing restraints and head entrapment gap

    About 4,300 Harppa 5-in-1 convertible high chairs are being recalled because they were sold without the required restraint system and a child's head can become trapped between seat and tray.

    Product
    Harppa 5-in-1 Convertible High Chairs for Babies and Toddlers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26055·2025-10-30

    YaFiti fabric dressers recalled over tip over and entrapment hazards

    About 6,880 YaFiti fabric 12-drawer dressers are being recalled because they are unstable when not anchored to a wall and violate the STURDY Act standard.

    Product
    YaFiti Fabric 12-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V744000·2025-10-30

    Toyota, Lexus, and Subaru vehicles with defective panoramic rearview camera

    Toyota Motor Engineering & Manufacturing is recalling 2022–2026 Toyota, Lexus, and Subaru vehicles with a Panoramic View Monitor system due to a software error that may freeze or blank the rearview camera in reverse, reducing rear visibility and increasing crash risk.

    Product
    LEXUS — LEXUS, TOYOTA, SUBARU LC HYBRID, TX HYBRID, VENZA HYBRID, BZ4X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·26057·2025-10-30

    Glow stick bracelets recalled because green bracelet can leak and irritate

    About 6,600 Destination Holiday Glow Light Stick bracelet 12-packs are being recalled because the green bracelet can leak, posing a skin irritation hazard.

    Product
    Destination Holiday Glow Light Stick Bracelets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0087-2026·2025-10-29

    Large mozzarella penne salads recalled over potential Listeria from supplier

    Giant Eagle is recalling 16 lbs of large Smoked Mozzarella Penne Salad after a recall notification from its supplier about potential Listeria contamination.

    Product
    Smoked Mozzarella Penne Salad-Large, Clam shell and Bowl, 9 lbs, Individual Unit, Keep Refrigerated, UPC 246512000000
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·H-0094-2026·2025-10-29

    Basil pesto bowtie salad recalled over recalled pasta ingredient and Listeria

    Kroger is recalling 5,567.4 lbs of Basil Pesto Bowtie Pasta Salad because the store-made deli item contains a pasta ingredient recalled for potential Listeria monocytogenes.

    Product
    Basil Pesto Bowtie Pasta Salad, packaged in plastic containers with various weights, with UPC 217573-1XXXX (sold at deli service counters) or UPC 217573-2XXXX (sold as Grab-n-Go packages in deli departments), under the banners Kroger, Baker's, City Market, Dillons, Fred Meyer, Fr
    Category
    Food
    Distribution
    28 states
  • CriticalFDA (Food)·H-0090-2026·2025-10-29

    Bowtie pasta kits recalled over potential Listeria monocytogenes contamination

    Reser's Fine Foods is recalling 3,252 cases of Fresh Creative Foods Basil Pesto Bowtie Pasta Kit for potential contamination with Listeria monocytogenes.

    Product
    Fresh Creative Foods (FCF) item #404637 Basil Pesto Bowtie Pasta Kit Item V, UPC#13454 38053. Perishable/Refrigerated product. Net wt. 10.5625lbs. This kit contains 2/3lbs. sealed bags of affected Bowtie Pasta, and it is not sold directly to consumers.
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·H-0088-2026·2025-10-29

    Deli pasta salad recalled because it may contain Listeria monocytogenes

    Sprouts Farmers Market is recalling Smoked Mozzarella Pasta Salad sold at deli counters and in grab-and-go containers because the product may contain Listeria monocytogenes.

    Product
    Sprouts Smoked Mozzarella Pasta Salad, RTE Pasta Salad, Refrigerated, 5 day shelf life, packaged into plastic containers at Deli counter and into 16oz plastic grab & go containers, weight dependent on customer request, UPC 2-15587-00000 (from service case) and 2-15786-00000 (from
    Category
    Food
    Distribution
    24 states
  • CriticalFDA (Food)·H-0117-2026·2025-10-29

    Pesto bowtie pasta salad recalled over Listeria in recalled ingredient

    Albertsons Companies is recalling Ready Meals Pesto Bowtie Pasta Salad sold under six banners because it contains a bowtie pasta ingredient recalled for Listeria monocytogenes.

    Product
    READY MEALS Pesto Bowtie Pasta Salad, UPC 27133 #####. Product was made in-store with store generated scale label applied to the container. Sold under store banners Albertsons, Pavilions, Randalls, Safeway, Tom Thumb, and Vons in AR, AZ, CA, CO, LA, NE, NM, NV, OK, SD, TX, UT
    Category
    Food
    Distribution
    15 states
  • CriticalFDA (Food)·H-0149-2026·2025-10-29

    Breakfast burritos recalled after cooked egg ingredient tested positive for Listeria

    M.C.I. Foods is recalling 330 cases of Cheese and Egg with Green Salsa Breakfast Burritos after the cooked egg ingredient tested positive for Listeria monocytogenes.

    Product
    Cheese and Egg with Green Salsa Breakfast Burrito; 3.75 oz; 72 count/case; UPC# 1 070657 468334 8
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0118-2026·2025-10-29

    Basil pesto bowtie salad recalled over Listeria in recalled pasta ingredient

    Albertsons Companies is recalling its store-made Basil Pesto Bowtie Pasta Salad because it contains a bowtie pasta ingredient recalled for Listeria monocytogenes.

    Product
    Basil Pesto Bowtie Pasta Salad, UPC 294921 #####. Product was made in-store with store generated scale label applied to the container. Sold under store banners Albertsons, Pavilions, Randalls, Safeway, Tom Thumb, and Vons in AR, AZ, CA, CO, LA, NE, NM, NV, OK, SD, TX, UT, and W
    Category
    Food
    Distribution
    15 states
  • CriticalFDA (Food)·H-0124-2026·2025-10-29

    Mozzarella and hot links meals recalled over Listeria in pasta ingredient

    Albertsons Companies is recalling its store-made Ready Meals Smoked Mozzarella With Hot Links Extra Large because it contains a penne pasta ingredient recalled for Listeria.

    Product
    Ready Meals Smoked Mozzarella With Hot Links Extra Large, UPC 200003 #####. Product was made in-store with store generated scale label applied to the container. Sold under store banners Carrs-Safeway, Eagle, and Safeway in AK
    Category
    Food
    Distribution
    15 states
  • CriticalFDA (Food)·H-0095-2026·2025-10-29

    Kroger penne salad recalled over Listeria in recalled pasta ingredient

    Kroger is recalling 25,792 lbs of store-made Smoked Mozzarella Penne Salad because it contains a pasta ingredient recalled for potential Listeria monocytogenes.

    Product
    Smoked Mozzarella Penne Salad, packaged in plastic containers with various weights, with UPC 227573-1XXXX (sold at deli service counters) or UPC 227573-2XXXX (sold as Grab-n-Go packages in deli departments), under the banners Kroger, Baker's, City Market, Dillons, Fred Meyer, Fry
    Category
    Food
    Distribution
    28 states
  • CriticalFDA (Food)·H-0121-2026·2025-10-29

    Spinach bowtie pasta salad recalled over Listeria in pasta ingredient

    Albertsons Companies is recalling Ready Meals Spinach Bowtie Pasta Salad because the store-made deli item contains a bowtie pasta ingredient recalled for Listeria monocytogenes.

    Product
    Ready Meals Spinach Bowtie Pasta Salad, UPC 211426 #####. Product was made in-store with store generated scale label applied to the container. Sold under store banners Albertsons, Amigos, Market, Market Street, and United in NY and TX.
    Category
    Food
    Distribution
    15 states
  • CriticalFDA (Devices)·Z-0154-2026·2025-10-29

    IV burette sets recalled over missing internal shutoff valve component

    ICU Medical is recalling 23,203 IV administration sets because the burette component is missing an internal shutoff valve intended to stop fluid flow.

    Product
    IV Administration sets. 23" (58 cm) 150 mL Burette Set (Clave, Shut Off) w/Clave, Luer Lock, REF: B33359; 23" (58 cm) 150 ml Burette Set (w/Shut Off), MicroClave, Clamp, REF: B9213; 70" (178 cm) 150 ml Burette Set (Clave, Shut-Off) w/3-Way Stopcock, Clave, Graduated Adapter,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0070-2026·2025-10-29

    Hemodialysis bloodline sets recalled over micro air bubbles from damaged connectors

    B. Braun is recalling Streamline Bloodline Sets for Dialog because damaged arterial and venous patient connectors may cause micro-air bubbles in the bloodline and air-in-line alarms.

    Product
    Brand Name: Hemodialysis Bloodlines Product Name: STREAMLINE BLOODLINE SET FOR DIALOG Model/Catalog Number: SL-2010M2096 Software Version: N/A Product Description: STREAMLINE BLOODLINE SET FOR DIALOG Component: N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0125-2026·2025-10-29

    Penne salad kits recalled over Listeria in recalled pasta ingredient

    Albertsons Companies is recalling its store-made Smoked Mozzarella Penne Salad Kit because it contains a penne pasta ingredient recalled for Listeria monocytogenes.

    Product
    Smoked Mozzarella Penne Salad Kit, UPC 271876 #####. Product was made in-store with store generated scale label applied to the container. Sold under store banners Carrs-Safeway, Eagle, and Safeway in AK.
    Category
    Food
    Distribution
    15 states
  • CriticalFDA (Devices)·Z-0136-2026·2025-10-29

    Impella controllers recalled over purge pressure issues from retainer failures

    Abiomed is recalling Automated Impella Controllers over the potential for purge pressure issues caused by purge retainer failures, covering 9,177 distributed units.

    Product
    Automated Impella Controller (AIC) labeled as the following with corresponding Product Codes: 1. AIC w/Impella Connect for ECP, Product Code: 1000432. 2. Dbl optical, AIC Impella Connect, Phg US, Product Code: 1000201. 3. Impella Controller, Packaged, AU, Product Code: 0042-00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0184-2026·2025-10-29

    Shanghai style noodles recalled for undeclared egg and two color additives

    Twin Marquis is recalling 5,080 packages of Thick Shanghai Style Plain Noodle because the product contains undeclared egg, FD&C Yellow 5 and FD&C Yellow 6.

    Product
    Twin Marquis brand THICK SHANGHAI STYLE PLAIN NOODLE; NET WT 16 OZ; Ingredients: Bleached Wheat Flour, Water, Corn Starch, Salt, Sodium Benzoate (For Freshness); Contains: Wheat.; Produced on machinery that uses eggs; Manufactured by: Twin Marquis Inc. Brooklyn, NY 11206; UPC 7 6
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·H-0086-2026·2025-10-29

    Small mozzarella penne salads recalled over potential Listeria from supplier

    Giant Eagle is recalling 27 lbs of Smoked Mozzarella Penne Salad in small clamshells and bowls after a recall notification from its supplier about potential Listeria contamination.

    Product
    Smoked Mozzarella Penne Salad-Small, Clam shell and Bowl, 4 lbs 8 oz, Individual Unit, Keep Refrigerated, UPC 246511000000
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·H-0120-2026·2025-10-29

    Ready meals pesto bowtie salad recalled over Listeria in pasta

    Albertsons Companies is recalling Ready Meals Basil Pesto Bowtie Pasta Salad sold under its Alaska banners because it contains a bowtie pasta ingredient recalled for Listeria.

    Product
    Ready Meals Basil Pesto Bowtie Pasta Salad, UPC 291308 #####. Product was made in-store with store generated scale label applied to the container. Sold under store banners Carrs-Safeway, Eagle, and Safeway in AK.
    Category
    Food
    Distribution
    15 states
  • CriticalFDA (Food)·H-0091-2026·2025-10-29

    Penne salad kits recalled over potential Listeria monocytogenes contamination

    Reser's Fine Foods is recalling 4,770 cases of Fresh Creative Foods Smoked Mozzarella Penne Salad Kit for potential contamination with Listeria monocytogenes.

    Product
    Fresh Creative Foods (FCF) item #404284 Smoked Mozzarella Penne Salad Kit, UPC #13454 37904. Perishable/Refrigerated product. Net wt. 13lbs. This kit contains 2/3lbs. sealed bag of affected Penne Pasta and kit is not sold directly to consumers.
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·H-0132-2026·2025-10-29

    Shrimp scampi meals recalled over linguine linked to Listeria outbreak

    Demers Food Group is recalling 12,962 cases of Scott & Jon's Shrimp Scampi with Linguine because it contains linguine recalled for Listeria monocytogenes and implicated in an ongoing outbreak.

    Product
    Scott & Jon s Shrimp Scampi with Linguine, 9.6 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0089-2026·2025-10-29

    Spinach free bowtie pasta kits recalled over potential Listeria contamination

    Reser's Fine Foods is recalling 795 cases of Fresh Creative Foods Basil Pesto Bowtie Pasta Kit for potential contamination with Listeria monocytogenes.

    Product
    Fresh Creative Foods (FCF) item #404736 Basil Pesto Bowtie Pasta Kit, UPC #13454 38092. Perishable/Refrigerated product. Net wt. 10.3125lbs. This kit contains 2/3lb. sealed bags of affected Bowtie Pasta and does not contain spinach. Kit is not sold directly to consumers.
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·H-0119-2026·2025-10-29

    Store-made pesto bowtie salad recalled over Listeria in pasta ingredient

    Albertsons Companies is recalling Basil Pesto Bowtie Pasta Salad sold under its California, Hawaii and Nevada banners because it contains a bowtie pasta ingredient recalled for Listeria.

    Product
    Basil Pesto Bowtie Pasta Salad, UPC 216492 #####. Product was made in-store with store generated scale label applied to the container. Sold under store banners Andronico's Community, Markets, Pak'N Save, Safeway, and Vons in CA, HI, and NV.
    Category
    Food
    Distribution
    15 states
  • CriticalFDA (Food)·H-0150-2026·2025-10-29

    Breakfast burritos and wraps recalled after egg ingredient tested positive for Listeria

    M.C.I. Foods is recalling 1,040 cases of Egg and Cheese Breakfast Burritos and Wraps after the cooked egg ingredient tested positive for Listeria monocytogenes.

    Product
    Egg and Cheese Breakfast Burrito; 3.75 oz; 72 count/case; UPC# 1 070657 477333 9 RTE Egg and Cheese Breakfast Wrap; 2.50 oz; 72 count/case; UPC# 1 070657 497861 1
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0123-2026·2025-10-29

    Grilled chicken basil pasta recalled over Listeria in bowtie pasta ingredient

    Albertsons Companies is recalling its store-made Grilled Chicken & Basil Pasta Extra Large because it contains a bowtie pasta ingredient recalled for Listeria monocytogenes.

    Product
    Grilled Chicken & Basil Pasta Extra Large UPC 213035 #####. Product was made in-store with store generated scale label applied to the container. Sold under store banners Carrs-Safeway, Eagle, and Safeway in AK
    Category
    Food
    Distribution
    15 states
  • CriticalFDA (Food)·H-0122-2026·2025-10-29

    Basil bowtie pasta salad recalled over Listeria in pasta ingredient

    Albertsons Companies is recalling Ready Meals Basil Bowtie Pasta Salad because the store-made deli item contains a bowtie pasta ingredient recalled for Listeria monocytogenes.

    Product
    Ready Meals Basil Bowtie Pasta Salad, UPC 211913 #####. Product was made in-store with store generated scale label applied to the container. Sold under store banners Albertsons, Market, Amigos, Market Street, and United in NM and TX.
    Category
    Food
    Distribution
    15 states
  • CriticalFDA (Food)·H-0126-2026·2025-10-29

    Store-made penne pasta salad recalled over Listeria in pasta ingredient

    Albertsons Companies is recalling Ready Meals Smoked Mozzarella Penne Pasta Salad because the store-made deli item contains a penne pasta ingredient recalled for Listeria monocytogenes.

    Product
    Ready Meals Smoked Mozzarella Penne Pasta Salad, UPC 291298 #####. Product was made in-store with store generated scale label applied to the container. Sold under store banners Carrs-Safeway, Eagle, and Safeway in AK.
    Category
    Food
    Distribution
    15 states
  • SevereNHTSA·25V737000·2025-10-29

    Mazda CX-50 front suspension bolts may allow wheel detachment

    Mazda is recalling certain 2025 CX-50 and CX-50 Hybrid vehicles because the front suspension fastener bolts may not be tightened properly, which can result in suspension component or wheel detachment.

    Product
    MAZDA — MAZDA CX-50, CX-50 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0295-2026·2025-10-29

    Elscint Helix gamma cameras recalled over risk of detector falling

    GE HealthCare is recalling three Elscint Helix gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Elscint Helix; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0206-2026·2025-10-29

    ENFit sump tubes recalled after anti-reflux valve breakage complaints

    Cardinal Health is recalling all lots of ENFit Salem Sump PVC tubes after complaints of anti-reflux valve breakage due to excessive force during use.

    Product
    Salem Sump PVC Tubes: Product Code/Product Name: 8888264911E ENFit" SALEM SUMP" PVC TUBE 10FR 36IN 8888264929E ENFit" SALEM SUMP" PVC TUBE 12FR 48IN 8888264945E ENFit" SALEM SUMP" PVC TUBE 14FR 48IN 8888264960E ENFit" Salem Sump" PVC Tube 16Fr 48IN 8888264986E ENFit" SA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0240-2026·2025-10-29

    Veritor Connect software recalled after service credentials accessed by unauthorized actor

    Becton Dickinson is recalling 38 BD Veritor Connect Software units after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD Veritor Connect Software, labeled as the following: 1. Veritor (NUC), Catalog Number: 444881. Transfers in vitro diagnostic results data on the BD Veritor Plus Analyzer to BD Synapsys.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0239-2026·2025-10-29

    Automated microbiology systems recalled after service credentials were accessed by unauthorized actor

    Becton Dickinson is recalling 4,283 BD Phoenix M50 Automated Microbiology Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD Phoenix M50 Instrument, labeled as the following: 1. BD Phoenix M50 Automated Microbiology System, Catalog Numbers: 443624, 44362409.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0301-2026·2025-10-29

    Optima NX gamma camera recalled over risk of detector falling

    GE HealthCare is recalling one Optima NX gamma camera because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Optima NX; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0238-2026·2025-10-29

    BD MAX instruments recalled after service credentials accessed by unauthorized actor

    Becton Dickinson is recalling 62 BD MAX System instruments after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD MAX System, for in vitro diagnostic (IVD) use, labeled as the following: 1. BD MAX System, BD MAX Instrument, Catalog Numbers: 44191609, 441927.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0302-2026·2025-10-29

    Sopha Medical Vision cameras recalled over risk of detector falling

    GE HealthCare is recalling 205 Sopha Medical Vision gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Sopha Medical Vision (SMV) DSXi/DST-XLi,/ DST-XL/ DSTi; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0211-2026·2025-10-29

    Gastroduodenal sump tubes recalled after anti-reflux valve breakage complaints

    Cardinal Health is recalling all lots of Salem Sump PVC gastroduodenal tubes after complaints of anti-reflux valve breakage due to excessive force during use.

    Product
    Salem Sump PVC Tubes: Product Code/Product Name: 1180264408 Salem Sump" PVC Gastroduodenal Tube, 10 Fr/Ch (3.3 mm) x 90 cm 1180264416 Salem Sump" PVC Gastroduodenal Tube, 12 Fr/Ch (4.0 mm) x 114 cm 1180264424 Salem Sump" PVC Gastroduodenal Tube, 14 Fr/Ch (4.7 mm) x 114 cm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0296-2026·2025-10-29

    Maxicam gamma cameras recalled over risk of detector falling from mount

    GE HealthCare is recalling 37 Maxicam gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Maxicam; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0288-2026·2025-10-29

    Defibrillator pad packs recalled over damaged pins disrupting electrical contact

    HeartSine Technologies is recalling 1,291,165 Pad-Pak units because defibrillator pads may contain damaged pins that disrupt the mechanical fit and electrical contact.

    Product
    HeartSine Pad-Pak, REF: PAD-PAK-01, PAD-PAK-02, PAD-PAK-03, PAD-PAK-04, PAD-PAK-07, PAD-PAK-03J, PAD-PAK-04J
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0208-2026·2025-10-29

    Silicone stomach tubes recalled after anti-reflux valve breakage complaints

    Cardinal Health is recalling all lots of Salem Sump silicone dual lumen stomach tubes after complaints of anti-reflux valve breakage due to excessive force during use.

    Product
    Salem Sump PVC Tubes: Product Code/Product Name: 8888265108 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 10 Fr/Ch (3.3 mm), 36 (91 cm) 8888265116 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 12 Fr/Ch (4.0 mm), 48 (122 cm) 8888265124 Salem
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0234-2026·2025-10-29

    Prefilled saline flush syringes recalled over sodium chloride concentration shortfall

    Medline is recalling 8,267,150 Excelsior Medical 0.9% Sodium Chloride prefilled flush syringes because a limited quantity may not meet the required concentration of sodium chloride.

    Product
    Excelsior Medical, 0.9% Sodium Chloride Injection, USP - 10 mL Fill, Item Number EMZ111240. Prefilled saline flush syringes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0298-2026·2025-10-29

    Millenium Myosight gamma cameras recalled over risk of detector falling

    GE HealthCare is recalling 82 Millenium Myosight gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Millenium Myosight; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0300-2026·2025-10-29

    Millenium MPS gamma cameras recalled over risk of detector falling

    GE HealthCare is recalling 54 Millenium MPS gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Millenium MPS; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0299-2026·2025-10-29

    Millenium MPR gamma cameras recalled over risk of detector falling

    GE HealthCare is recalling 292 Millenium MPR gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Millenium MPR; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·H-0127-2026·2025-10-29

    Dubai style chocolate recalled because wheat is not declared as allergen

    Rolling Pin Baking Company is recalling 127,680 units of Rolling Pin Dubai Style Chocolate because the product does not declare wheat in the allergen statement.

    Product
    Rolling Pin brand Dubai Style Chocolate; 17.64 oz stand up pouch; Ingredients: Sugar, Cocoa Butter, Vegetable Fats, Whole Milk Powder, Pistachio (Tree Nut), Skimmed Milk Powder, Cocoa Mass, Kunefa, Soy Lecithin, Natural Vanilla Powder; Allergens: Contains Milk, Soy, Nuts (Pistach
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·H-0140-2026·2025-10-29

    Shredded imitation crabmeat recalled over potential Clostridium botulinum from temperature abuse

    Ocean's Kitchen is recalling 496 cases of shredded imitation crabmeat for potential contamination with Clostridium botulinum due to a risk of temperature abuse during chilled storage at the firm.

    Product
    Oceans Kitchen IMITATION CRABMEAT SHREDDED Made From Wild Fish, Refrigerated, vacuum package. Net wt. per bag 2.5 lbs. UPC 1 90456 75654 2. These 2.5lb. bags are not for retail sales. Each master case contains 12/2.5lbs. bags. Net wt. per case: 30lbs. UPC 14972195756549. Oceans
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0209-2026·2025-10-29

    Gastric sump anti-reflux valves recalled after breakage complaints from excessive force

    Cardinal Health is recalling all lots of Salem Sump Anti-Reflux Valves after complaints of valve breakage due to excessive force during use, and is providing additional guidance for use.

    Product
    Salem Sump PVC Tubes: Product Code/Product Name: 266197 Salem Sump" Anti-Reflux Valve CE Marked 8888266197 Salem Sump" Anti-Reflux Valve
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0294-2026·2025-10-29

    Elscint Varicam gamma cameras recalled over risk of detector falling

    GE HealthCare is recalling 15 Elscint Varicam gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Elscint Varicam; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·H-0114-2026·2025-10-29

    Frozen cooked salad shrimp recalled over possible cesium 137 contamination

    Southwind Foods is recalling Arctic Shores branded frozen cooked salad shrimp in 6 oz bags because it may have been contaminated with Cesium-137.

    Product
    Arctic Shores branded Frozen cooked salad shrimp; 6 oz bag UPC: 041130811685
    Category
    Food
    Distribution
    34 states
  • HighFDA (Devices)·Z-0292-2026·2025-10-29

    Elscint SPX4 gamma cameras recalled over risk of detector falling

    GE HealthCare is recalling 45 Elscint SPX4 gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Elscint SPX4; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0303-2026·2025-10-29

    Nuclear medicine gamma cameras recalled over risk of detector falling from mount

    GE HealthCare is recalling 102 Starcam and Camstar gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Starcam/Camstar; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0212-2026·2025-10-29

    AC joint fixation implants recalled over potentially missing slotted button assembly

    Biomet is recalling 98 ZipTight Acute AC Joint Implants from one lot because of the potential for a missing slotted button assembly.

    Product
    BIOMET ZipTight, Acute AC Joint Implant, Single Ziploop , Model/Catalog Number: 904834; Fixation System for AC Joint Repair
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0215-2026·2025-10-29

    Clinical analyzer modules recalled over dilution factor software anomaly affecting results

    Beckman Coulter is recalling 160 DxC 500i Clinical Analyzer modules over a software anomaly that may not apply user-specified manual dilution factors, risking false low or high results.

    Product
    DxC 500i Clinical Analyzer Modules, DxC 500 AU Module w/ISE, DxC 500i (Part Number C63522), DxC 500 AU Module, DxC 500i (Part Number C63521), and Access 2 Module, DxC 500i (Part Number C13252)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0115-2026·2025-10-29

    Tovala frozen raw shrimp recalled over possible cesium 137 contamination

    Southwind Foods is recalling Tovala branded frozen raw phosphate free shrimp in 5 oz bags because it may have been contaminated with Cesium-137.

    Product
    Tovala branded Frozen raw phosphate free shrimp; 5oz IQF bag UPC: 829944085788
    Category
    Food
    Distribution
    34 states
  • HighFDA (Devices)·Z-0227-2026·2025-10-29

    Bipolar hip heads recalled downstream after femoral components failed transit testing

    Theken Companies is recalling 409 iNSitu Bipolar Hip System head assemblies in a downstream recall after BioPro femoral components failed transit testing, risking sterile barrier issues.

    Product
    iNSitu Bipolar Hip System, Bipolar head implant Part ID Description 10-22-0038 Bipolar Head Assembly, Size 38mm 10-22-0040 Bipolar Head Assembly, Size 40mm 10-22-0042 Bipolar Head Assembly, Size 42mm 10-22-0044 Bipolar Head Assembly, Size 44mm 10-22-0046 Bipolar Head Asse
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0097-2026·2025-10-29

    Long grain white ready rice recalled over possible stones in product

    Mars Foods US is recalling 273 cases of Ben's Original Ready Rice Original Long Grain White because of the possible presence of stones in the product.

    Product
    Ben's Original Ready Rice Original Long Grain White, 8.8oz., UPC 0 54800 42333 0. 12 retail units per wholesale case
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-0213-2026·2025-10-29

    Central stations recalled over reboot loop that halts patient monitoring

    GE HealthCare is recalling 173 Carescape Central Stations running software V3.0.5 because the system can enter a continuous reboot cycle, losing central monitoring of connected patients.

    Product
    GE Healthcare Carescape Central Station (CSCS) V3 MAS800 Desktop with software version V3.0.5; Part Number 5867474-04; Medical Display, cathode ray tube
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0237-2026·2025-10-29

    Blood culture systems recalled after service credentials were accessed by unauthorized actor

    Becton Dickinson is recalling 1,086 BD BACTEC Blood Culture Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD BACTEC Blood Culture System, labeled as the following: 1. BACTEC 9120 System, Catalog Numbers: 445570, 445702. 2. INSTRUMENT BACTEC 9120 UNREPAIRED, Catalog Number: 44557008.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0291-2026·2025-10-29

    Elscint 4XX gamma cameras recalled over risk of detector falling

    GE HealthCare is recalling 64 Elscint Model 4XX gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.

    Product
    Elscint Model 4XX; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·H-0107-2026·2025-10-29

    Coca-Cola cans recalled over potential presence of metal foreign material

    Coca-Cola Southwest Beverages is recalling 2,322 units of Coca-Cola 12 oz cans in Texas over the potential presence of metal foreign material.

    Product
    Coca-Cola 12oz Can - 24 pack 49000012781 / JUN2926MAA Coca-Cola 12oz Can - 35 pack 49000058468 / JUN2926MAA
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0097-2026·2025-10-29

    Opdualag injection vials recalled from one lot over sterility assurance

    Bristol-Myers Squibb is recalling 12,778 vials of Opdualag (nivolumab and relatlimab-rmbw) injection from one lot for lack of assurance of sterility.

    Product
    OPDUALAG — OPDUALAG (NIVOLUMAB AND RELATLIMAB-RMBW)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0207-2026·2025-10-29

    PVC stomach tubes recalled after anti-reflux valve breakage complaints

    Cardinal Health is recalling all lots of Salem Sump dual lumen stomach tubes after complaints of anti-reflux valve breakage due to excessive force during use.

    Product
    Salem Sump PVC Tubes: Product Code/Product Name: 264929 Salem Sump" Stomach Tube, Dual Lumen, 12 Fr/Ch (4.0 mm) 264945 Salem Sump" Stomach Tube, Dual Lumen, 14 Fr/Ch (4.7 mm) 264960 Salem Sump" Stomach Tube, Dual Lumen, 16 Fr/Ch (5.3 mm) 264986 Salem Sump" Stomach Tube, Du
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0216-2026·2025-10-29

    Immunoassay analyzers recalled over dilution factor anomaly affecting patient results

    Beckman Coulter is recalling 571 DxI 9000 Access Immunoassay Analyzers over a software anomaly that may not apply user-specified manual dilution factors, risking false low or high results.

    Product
    DxI 9000 Access Immunoassay Analyzer, Part Number C11137
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0083-2026·2025-10-29

    Jumbo meatball subs recalled over metal shavings in mozzarella ingredient

    MG Foods is recalling 117 Jumbo Meat Ball Subs because the mozzarella cheese ingredient has the potential to be contaminated with metal shavings.

    Product
    Jumbo Meat Ball Sub; Net Weight: 8.9oz; Product Code: Fresh Thru 10-15-25, 10/16/2025, 10/20/2025 In clear plastic packaging with white sticker label
    Category
    Food
    Distribution
    2 states

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