The Recall Desk

Archive

October 2025 recalls

804 recalls were announced in October 2025.

What the numbers show

Critical
178
Severe
79
High
390
Moderate
154
Low
3

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

Which agencies issued them

401–500 of 804

  • ModerateFDA (Drugs)·D-0027-2026·2025-10-22

    Sucralfate tablets recalled after bankruptcy left quality program unmonitored

    Amerisource Health Services is recalling 27,868 blister packs of Sucralfate Tablets USP 1 gram because, after a Chapter 11 filing, the firm cannot monitor its quality program.

    Product
    Sucralfate Tablets, USP 1 gram, 100 Tablets, (10x10), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217, NDC 60687-695-01 - Carton NDC [60687-695-11- Unit Dose]
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0026-2026·2025-10-22

    Everolimus tablets recalled for out of specification impurity in one lot

    Endo USA is recalling 1,041 cartons of Everolimus tablets 5mg after the lot returned an out-of-specification result for impurity IP-C.

    Product
    Everolimus tablets 5mg, 28 tablets (each carton contains 4 blister strips with 7 tablets each), Rx only, Manufactured by: Par Pharmaceutical Chestnut Ridge, NY 10977, NDC 49884-125-91
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0024-2026·2025-10-22

    Ketamine syringes recalled over incorrect or missing lot and expiry

    STAQ Pharma is recalling one lot of Ketamine Hydrochloride 50mg/5 mL injection syringes because of incorrect or missing lot and expiration date information on the label.

    Product
    Ketamine Hydrochloride, 50mg/5 mL (10mg/mL), Injection for IV use, 50 mL syringe, STAQ Pharma Inc., 14135 E 42nd Ave, Denver, Colorado, NDC 73177-0156-02.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V716000·2025-10-21

    Ferrari Recalls 2025 296 GTS and GTB for Oil Leak Fire Risk

    Ferrari is recalling 2025 296 GTS and 296 GTB vehicles because an incorrectly tightened oil filter nut may cause an oil leak near combustible sources, increasing fire risk.

    Product
    FERRARI — FERRARI 296 GTS, 296 GTB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V718000·2025-10-21

    Motorhome paddle latch can lock owners out of the propane compartment

    REV Recreation Group is recalling certain 2024-2026 Holiday Rambler Invicta and Fleetwood Fortis RVs because a paddle latch may lock unintentionally, blocking access to the liquid propane compartment.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD INVICTA, FORTIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V715000·2025-10-21

    Fiat 500e headlight aim adjustment is not covered as intended

    Chrysler is recalling certain 2024-2025 Fiat 500e electric vehicles because the headlight horizontal aim adjustment is not covered as intended, which can leave the headlights improperly adjusted.

    Product
    FIAT — FIAT 500E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V717000·2025-10-21

    2026 BMW X2 and Related Vehicles Seat Belt Retractor Failure Recall

    BMW is recalling certain 2026 X2, X1, 2 Series Gran Coupe, and Mini Countryman S ALL4 vehicles because the rear seat belt retractors may not lock properly due to damage during production, increasing injury risk in a crash.

    Product
    MINI — MINI, BMW COUNTRYMAN S ALL4, X2, X1, 228I XDRIVE GRAN COUPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V713000·2025-10-20

    ACP Cryogenic Tank Trailer Recall for Improperly Welded Suspension Towers

    Alloy Custom Products is recalling 2023-2025 ACP cryogenic tank trailers because improperly welded suspension towers may cause axle detachment and increase crash risk.

    Product
    ACP — ACP CRYOGENIC TANK TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·032-2025·2025-10-18

    M.C.I. Foods Recalls Frozen Breakfast Burritos and Wraps Due to Listeria Risk

    M.C.I. Foods is recalling approximately 91,585 pounds of frozen breakfast burritos and wraps due to possible Listeria monocytogenes contamination.

    Product
    M.C.I. Foods, Inc. — M.C.I. Foods, Inc. Recalls Ready-To-Eat Breakfast Burrito and Wrap Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V710000·2025-10-17

    Jeep Wrangler 4XE software update can cause loss of drive power

    Chrysler is recalling certain 2023-2025 Jeep Wrangler 4XE plug-in hybrids because a software error in an over-the-air update may result in a loss of drive power. The remedy is still under development.

    Product
    JEEP — JEEP WRANGLER 4XE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V712000·2025-10-17

    Mercedes Sprinter radar sensor failure can disable automatic emergency braking

    Daimler Vans is recalling certain 2025 Mercedes-Benz Sprinter 2500 vehicles because the front short-range radar sensor circuit board may fail, causing a loss of automatic emergency braking.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V709000·2025-10-17

    Thor Motor Coach recreational vehicles with unsecured LP generator hose

    Thor Motor Coach is recalling certain 2025–2026 recreational vehicles because a P-clamp may not have been installed to secure the Liquid Propane (LP) generator hose, which could contact the exhaust and increase fire risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH GENEVA, QUANTUM, FOUR WINDS, PASADENA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V708000·2025-10-17

    Forest River Recalls 2026 Wildwood and Salem Travel Trailers for Fire Risk

    Forest River is recalling 2026 Wildwood and Salem travel trailers because the exterior griddle may be stowed while connected to the LP gas line, increasing fire risk.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V711000·2025-10-17

    Mercedes G-Class radar sensor failure can disable driver assistance systems

    Mercedes-Benz is recalling certain 2025 AMG G63 and G 580 vehicles because the front short-range radar sensor circuit board may fail, disabling automatic emergency braking and other assistance features.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ G 580 EV, AMG G63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·25V707000·2025-10-17

    Forest River trailer labels may list incorrect tire inflation information

    Forest River is recalling certain 2025-2026 Stealth EVO, RPOD, Wildwood and Salem trailers because the tire information label may list incorrect tire inflation information, risking overinflation.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, RPOD, STEALTH EVO, SALEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V706000·2025-10-16

    Alexis Fire Equipment Recalls Fire Trucks Due to Door Latch Defect

    Alexis Fire Equipment is recalling 22 fire trucks because a door latch defect may prevent the cab door from opening, potentially trapping occupants.

    Product
    ALEXIS FIRE EQUIPMENT — ALEXIS FIRE EQUIPMENT FIRE APPARATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26023·2025-10-16

    Stone dining tables and desks recalled after one collapsed causing lacerations

    About 750 RH Byron travertine and marble tables and desks are being recalled because they can collapse; one dining table collapse has caused lacerations.

    Product
    Byron Emperador Tables and Byron Reeded Stone Tables and Desks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26026·2025-10-16

    Gas boilers recalled after cracked exhaust ducts leaked fumes indoors

    About 36,700 VST-brand residential gas boilers are being recalled after 33 reports of cracked exhaust ducts allowing exhaust fumes to leak, posing a carbon monoxide poisoning hazard.

    Product
    VST gas-fired tankless water heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26025·2025-10-16

    Rowing machines recalled after screen consoles caught fire or melted

    About 44,800 iFIT NordicTrack rowing machines are being recalled because the screen console can overheat and ignite; eight incidents include two fires and at least $6,000 in property damage.

    Product
    NordicTrack Model NTRW19147 Rowing Machine
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V704000·2025-10-16

    Chevrolet Equinox EV tires can lose tread partially or fully

    General Motors is recalling certain 2025-2026 Chevrolet Equinox EV and Cadillac Optic vehicles with 21-inch Continental all-season tires because one or more tires may lose part or all of their tread.

    Product
    CADILLAC — CADILLAC, CHEVROLET OPTIQ, EQUINOX EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26028·2025-10-16

    Yamaha golf cars recalled for lacking stop lights on the vehicle

    About 19,300 model year 2021-2025 Yamaha Drive 2 personal transportation vehicles are being recalled because they lack stop lights. No incidents have been reported.

    Product
    Model Year 2021-2025 Yamaha Golf Car Vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26027·2025-10-16

    Yamaha golf cars recalled because the vehicles can fail to brake

    About 4,300 model year 2017-2024 Yamaha DR2A and DR2E personal transportation vehicles are being recalled because they can fail to brake. No incidents have been reported.

    Product
    Model Year 2017-2024 Yamaha Golf Car Vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V705000·2025-10-16

    Land Rover and Jaguar Recall Vehicles for Gear Indicator Failure

    Jaguar Land Rover is recalling specific 2025-2026 models because moisture in the gear shift module may cause the gear position indicator light to fail, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER, JAGUAR RANGE ROVER SPORT, DISCOVERY SPORT, redundant RANGE ROVER, RANGE ROVER EVOQUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26021·2025-10-16

    Personal transportation vehicles recalled over fuel leak at injector fitting

    About 90,800 E-Z-GO personal transportation vehicles are being recalled because fuel can leak at the quick-connect fitting between the fuel line and the fuel injector.

    Product
    E-Z-GO Personal Transportation Vehicles (PTVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0029-2026·2025-10-15

    Nitric oxide systems recalled over fault from rapid button presses

    NOxBOX is recalling 1,667 NOxBOXi Nitric Oxide Delivery Systems because a rapid succession of button selections can trigger an unexpected internal fault or system diagnostic error.

    Product
    NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I
    Category
    Medical Device
    Distribution
    1 state
  • CriticalFDA (Food)·H-0077-2026·2025-10-15

    Cooked penne pasta recalled over potential Listeria monocytogenes contamination

    Nate's Fine Foods is recalling 1,337 cases of Fresh Creative Foods cooked penne, totaling 32,088 lbs, for potential contamination with Listeria monocytogenes.

    Product
    FRESH CREATIVE FOODS COOKED PENNE PASTA 8 x 3 lb pouches Net Weight: 24 lbs (10.88 kg) PERISHABLE KEEP REFRIGERATED
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·H-0079-2026·2025-10-15

    Cooked rotini pasta recalled over potential Listeria monocytogenes contamination

    Nate's Fine Foods is recalling 383 cases of Taylor Farms cooked rotini, totaling 9,192 lbs, for potential contamination with Listeria monocytogenes.

    Product
    TAYLOR FARMS COOKED ROTINI MAP 8 X 3 lb pouches Net Weight: 24 lbs (10.88 kg) PERISHABLE KEEP REFRIGERATED
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·H-0030-2026·2025-10-15

    Cinnamon Texas toast recalled for undeclared milk from cheese and butter

    Harris Teeter is recalling 83 units of its Cinnamon Texas Toast after finding that cheese and butter were left off the ingredient statement, so milk was not declared.

    Product
    Harris Teeter CINNAMON TEXAS TOAST, NET WT 5.0oz (0.31g), INGREDIENTS BREAD*** CONTAINS WHEAT, UPC 0 72036 95734 4, Harris Teeter Raleigh, NC
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·H-0076-2026·2025-10-15

    Cooked farfalle pasta recalled again over potential Listeria monocytogenes contamination

    Nate's Fine Foods is recalling 1,442 cases of Fresh Creative Foods cooked farfalle, totaling 34,068 lbs, for potential contamination with Listeria monocytogenes.

    Product
    FRESH CREATIVE FOODS COOKED FARFALLE PASTA 8 x 3 lb pouches Net Weight: 24 lbs (10.88 kg) PERISHABLE KEEP REFRIGERATED
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Devices)·Z-0028-2026·2025-10-15

    Nitric oxide delivery systems recalled over dose fluctuations at low flow

    NOxBOX is recalling 1,667 NOxBOXi Nitric Oxide Delivery Systems because delivered dose may fluctuate when total flow through the device sensor falls below its 0.5 LPM minimum.

    Product
    NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I
    Category
    Medical Device
    Distribution
    1 state
  • CriticalFDA (Devices)·Z-0069-2026·2025-10-15

    Heart pump controllers recalled over potential operating system cybersecurity vulnerabilities

    Abiomed is recalling 10,153 Automated Impella Controllers over potential cybersecurity vulnerabilities related to the controller's operating system.

    Product
    Automated Impella Controller (AIC), used for left heart support blood pump, labeled as the following with corresponding Product Codes: 1. Impella Controller, Packaged, AU; Product Code: 0042-0000-AU. 2. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA. 3.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0081-2026·2025-10-15

    Cooked trotolle pasta recalled over potential Listeria monocytogenes contamination

    Nate's Fine Foods is recalling 846 cases of Taylor Farms cooked trotolle, totaling 18,612 lbs, for potential contamination with Listeria monocytogenes.

    Product
    TAYLOR FARMS COOKED TROTOLLE MAP 8 X 2.75 lb pouches Net Weight: 22 lbs (9.97 kg) PERISHABLE KEEP REFRIGERATED
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·H-0011-2026·2025-10-15

    Shell eggs recalled over potential Salmonella contamination across four brands

    Country Eggs is recalling 81,542 dozen shell eggs sold under four brand names in California and Nevada because the product is potentially contaminated with Salmonella.

    Product
    o Nagatoshi Large AA Brown Omega-3 1 dozen cartons o Nijiya Large AA Brown Golden Yolk 1 dozen cartons o Mizuho Large AA Brown Omega-3 Cage 1 dozen cartons o Country Eggs Large AA Brown Sunshine Yolk 15 dozen bulk loose
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·H-0080-2026·2025-10-15

    Cooked farfalle pasta recalled over potential Listeria monocytogenes contamination

    Nate's Fine Foods is recalling 261 cases of Taylor Farms cooked farfalle, totaling 6,264 lbs, for potential contamination with Listeria monocytogenes.

    Product
    TAYLOR FARMS COOKED FARFALLE MAP 8 X 3 lb pouches Net Weight: 24 lbs (10.88 kg) PERISHABLE KEEP REFRIGERATED
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Devices)·Z-0035-2026·2025-10-15

    Infusion pump sets recalled over flow rate and occlusion alarm accuracy

    CareFusion is recalling BD Alaris Pump Infusion Sets because the pump module used with them may perform outside established ranges for flow rate, bolus accuracy and occlusion alarm timing.

    Product
    BD Alaris Pump Infusion Sets for the following reference numbers: C24101E, Amber Tubing, 15 Micron Filter, 0.2 Micron Filter, SmartSite Y-Site 10015414, 180 Micron Filter 2447-0007, Ball Valve SmartSite Port (Burette) 2 SmartSites Y-Sites 24201-0007, 2 SmartSite Y-sites…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0075-2026·2025-10-15

    Cooked fettuccine cases recalled over potential Listeria monocytogenes contamination

    Nate's Fine Foods is recalling 1,357 cases of MAP cooked fettuccine pasta, totaling 40,710 lbs, for potential contamination with Listeria monocytogenes.

    Product
    MAP COOKED FETTUCCINE PASTA 6 x 5 lbs pouches Net Weight: 30 lbs (13.60kg) PERISHABLE KEEP REFRIGERATED
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·H-0029-2026·2025-10-15

    Asiago Texas toast recalled for undeclared milk from cheese and butter

    Harris Teeter is recalling 295 units of its Asiago Texas Toast after finding that cheese and butter were left off the ingredient statement, so milk was not declared.

    Product
    Harris Teeter ASIAGO TEXAS TOAST, NET WT 5.0OZ (0.3lb), INGREDIENTS BREAD***CONTAINS WHEAT, UPC 0 72036 95364 3, Harris Teeter Raleigh, NC
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·H-0023-2026·2025-10-15

    Ahi tuna poke recalled after green onion supplier reported Listeria

    Western United Fish Company is recalling 3,314.7 lbs of Kirkland Signature Ahi Tuna Wasabi Poke after its green onion supplier reported a Listeria monocytogenes positive test result.

    Product
    Kirkland Signature brand Ahi Tuna Wasabi Poke, Costco #17193, net wt. 1lb. Product is packaged in clear plastic clamshell container and sold to consumers.
    Category
    Food
    Distribution
    37 states
  • CriticalFDA (Food)·H-0024-2026·2025-10-15

    Kimchi mackerel containers recalled for undeclared milk and shrimp allergens

    Lee K of NY is recalling 43 containers of Pinocchio Catering Aged Kimchi Mackerel because the product contains undeclared milk and shrimp.

    Product
    PINOCCHIO CATERING Aged Kimchi Mackerel; 57oz; 27330700000 in black bottomed plastic container
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Drugs)·D-0094-2026·2025-10-15

    NAD+ injection recalled after elevated endotoxin levels found in one lot

    GenoGenix is recalling NAD+ for Injection at 100 mg/mL and 200 mg/mL from one lot for microbial contamination of sterile products, with elevated endotoxin levels.

    Product
    NAD+ (Nicotinamide adenine dinucleotide) for Injection, a) 100 mg/mL b) 200 mg/mL, 10 mL multi-dose amber vials, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V700000·2025-10-15

    BMW Recalls 2018 328D Models Due to EGR Cooler Fire Risk

    BMW is recalling 2018 328D diesel vehicles because a leaking EGR cooler can cause smoldering particles and a melting intake manifold, increasing the risk of a fire.

    Product
    BMW — BMW 328D
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0088-2026·2025-10-15

    Tesamorelin injection recalled from one lot for lack of sterility assurance

    GenoGenix is recalling Tesamorelin for Injection, 15mg in a 10 mL multi-dose vial, from a single lot for lack of assurance of sterility.

    Product
    Tesamorelin for Injection, 15mg, 10 mL Multi-Dose Vial, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0046-2026·2025-10-15

    Bacteriostatic water for injection recalled over lack of sterility assurance

    GenoGenix is recalling Bacteriostatic Water for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    Bacteriostatic Water for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for CELIA Health, Extension Health and Medical Health Institute
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0061-2026·2025-10-15

    Lysine for injection recalled across all lots over sterility assurance

    GenoGenix is recalling Lysine for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    Lysine for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0040-2026·2025-10-15

    Ascorbic acid injection recalled across all lots for sterility assurance concerns

    GenoGenix is recalling preservative-free Ascorbic Acid (Vitamin C) for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    Ascorbic Acid (Vitamin C) for Injection, Preservative Free, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0052-2026·2025-10-15

    Glutathione magnesium injection recalled across all lots over sterility assurance

    GenoGenix is recalling Glutathione Magnesium for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    Glutathione Magnesium for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for CELIA Health.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0005-2026·2025-10-15

    Isopropyl hand sanitizer recalled because methanol risk could not be excluded

    Acuity Specialty Products is recalling AFCO isopropyl alcohol-based hand sanitizer because required receipt testing of incoming alcohol was not performed, so methanol risk could not be excluded.

    Product
    AFCO, Hand Sanitizer (Isopropyl Alcohol-Based, Product 5515), Manufactured by: AFCO, 550 Development Avenue, Chambersburg, PA 17201, Toll Free: 800-345-1329, Package Configuration: a) 4x1 Gallon Case, 5 Gallon Pail, 55 Gallon Drum.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0092-2026·2025-10-15

    Tirzepatide injection recalled from two lots over lack of sterility assurance

    GenoGenix is recalling Tirzepatide 60mg/10 mL for Injection from two lots for lack of assurance of sterility.

    Product
    Tirzepatide, 60mg/10 mL for Injection, 10mL vial lyophilized, all presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for Extension Health and Synergy Wellness 60mg, 10mL vial lyophilized.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·25V701000·2025-10-15

    Winnebago Recalls Travel Trailers Due to Incorrect Federal Tire Labeling

    Winnebago is recalling specific travel trailers because the Federal tire label may list the incorrect tire size, creating a risk of installing the wrong tire.

    Product
    WINNEBAGO — WINNEBAGO MINNIE PLUS5, MINNIE, MINNIE DROP, HIKE100
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0007-2026·2025-10-15

    Oral contraceptive tablets recalled after failing content uniformity specifications

    AvKARE is recalling 2,192 cartons of Norgestimate and Ethinyl Estradiol Tablets USP from one lot after the product failed content uniformity specifications.

    Product
    NORGESTIMATE AND ETHINYL ESTRADIOL — NORGESTIMATE AND ETHINYL ESTRADIOL (NORGESTIMATE AND ETHINYL ESTRADIOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0057-2026·2025-10-15

    L-Carnitine for injection recalled across all lots over sterility assurance

    GenoGenix is recalling L-Carnitine for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    L-Carnitine for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0084-2026·2025-10-15

    Zinc chloride injection recalled across all lots for lack of sterility

    GenoGenix is recalling Zinc Chloride for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    Zinc Chloride for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0083-2026·2025-10-15

    Semaglutide with B12 injection recalled across all lots over sterility

    GenoGenix is recalling Semaglutide with B12 for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    Semaglutide with B12 for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0071-2026·2025-10-15

    Cerebrolysin injection recalled across all lots for lack of sterility assurance

    GenoGenix is recalling Cerebrolysin for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    Cerebrolysin for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0047-2026·2025-10-15

    B-Complex injection recalled across all lots over lack of sterility assurance

    GenoGenix is recalling B-Complex for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    B-Complex for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. B-Complex with B12 also labeled as manufactured for Synergy Wellness.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0045-2026·2025-10-15

    Pyridoxine B6 injection recalled across all lots over sterility assurance

    GenoGenix is recalling B6 (Pyridoxine HCl) for Injections in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    B6 (Pyridoxine HCl) for Injections, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for Synergy Wellness
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0066-2026·2025-10-15

    Taurine for injection recalled across all lots over sterility assurance

    GenoGenix is recalling Taurine for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    Taurine for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0040-2026·2025-10-15

    Scleral reinforcement matrix recalled after complaints of early patch exposure

    CorNeat Vision is recalling 180 EverPatch+ units after reviewed complaints identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.

    Product
    EverPatch+, REF: 1044002, Permanent Scleral Reinforcement Matrix 1x5.0mm x 8.5 mm Shield/1 x 5.0mm x 6.5 mm Rectangle, STERILE VH202
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0080-2026·2025-10-15

    Buffered reconstitution solution recalled across all lots over sterility assurance

    GenoGenix is recalling pH Buffered Reconstitution Solution for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    pH Buffered Reconstitution Solution for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for Medical Health Institute (MHI), 10mL.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0107-2026·2025-10-15

    FlexLab X system recalled over unevaluated blood sample integrity function

    Inpeco is recalling one FlexLab X system because the Sample Integrity Module's hemolysis, icterus and lipemia function has not been evaluated by the FDA.

    Product
    FlexLab X (FXX) System. Potassium Test System. in vitro diagnostic
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Drugs)·D-0044-2026·2025-10-15

    Dexpanthenol B5 injection recalled across all lots over sterility assurance

    GenoGenix is recalling B5 Dexpanthenol for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    B5 Dexpanthenol for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0015-2026·2025-10-15

    Bulk Broadway mix recalled for missing label and four undeclared allergens

    Egress Capital Partners is recalling 3,547 cases of Taproom Gourmet 15 lb bulk Broadway Mix because the product has no ingredient label and contains undeclared peanuts, sesame, wheat and soy.

    Product
    Taproom Gourmet brand 15lb bulk "Broadway" Mix
    Category
    Food
    Distribution
    6 states
  • HighFDA (Drugs)·D-0076-2026·2025-10-15

    Low solubility peptide solution recalled across all lots over sterility assurance

    GenoGenix is recalling Low Solubility Peptide Reconstitution Solution for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    Low Solubility Peptide Reconstitution Solution for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.Also labeled as manufactured for CELIA Health.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0012-2026·2025-10-15

    Chlorpromazine tablets recalled over nitrosamine impurity above recommended intake limit

    Major Pharmaceuticals is recalling 866 blister packs of Chlorpromazine Hydrochloride Tablets USP 100 mg because N-Nitroso Desmethyl Chlorpromazine was present above the recommended intake limit.

    Product
    Major ChlorproMAZINE Hydrochloride Tablets, USP, 100 mg, 100 Tablets (10x10) blister package, Rx Only, Packaged and Distributed by Major Pharmaceuticals, Indianapolis, IN 46268, USA, NDC 0904-7132-61, UPC (01)00309047132614
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0049-2026·2025-10-15

    Calcium chloride injection recalled across all lots over sterility assurance

    GenoGenix is recalling Calcium Chloride for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    Calcium Chloride for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0129-2026·2025-10-15

    Shorter 8 French feeding tubes recalled because distal tips may detach

    Applied Medical Technology is recalling 840 NutraGlide 5 F - 8 F x 55 nasal feeding tubes whose distal tips may detach at lower than expected forces.

    Product
    NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 8 F x 55, REF E NRT-06055-I The NutraGlide Nasal Feeding Tube is a feeding tube placed through the nose and ending in the stomach or intestine used for the administration of nutrition, fluids, and medications in…
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·H-0071-2026·2025-10-15

    Cookies recalled over label that both declares and denies soy content

    Toto Foods is recalling 120,180 Toto S'Mores Ooey Gooey Cookies because the label contains conflicting statements about whether the product contains soy.

    Product
    Toto S'Mores Ooey Gooey Cookie; Gluten Free & Dairy Free; Net Wt. 2.25 OZ Rear panel: Packed with superfoods; Gluten, Dairy & Soy Free UPC: 860010409398
    Category
    Food
    Distribution
    14 states
  • HighFDA (Drugs)·D-0078-2026·2025-10-15

    Pentosan for injection recalled across all lots over sterility assurance

    GenoGenix is recalling Pentosan for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    Pentosan for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0009-2026·2025-10-15

    Chlorpromazine 25 mg fifty count packs recalled over nitrosamine impurity

    Major Pharmaceuticals is recalling 2,064 fifty-tablet blister packs of Chlorpromazine Hydrochloride Tablets USP 25 mg because a nitrosamine impurity exceeded the recommended intake limit.

    Product
    Major ChlorproMAZINE Hydrochloride Tablets, USP, 25 mg, 50 Tablets (5x10) blister package, Rx Only, Packaged and Distributed by Major Pharmaceuticals, Indianapolis, IN 46268, USA, NDC 0904-7130-06, UPC (01)00309047130061
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0011-2026·2025-10-15

    Chlorpromazine 50 mg tablets recalled over nitrosamine above recommended intake limit

    Major Pharmaceuticals is recalling 506 blister packs of Chlorpromazine Hydrochloride Tablets USP 50 mg because N-Nitroso Desmethyl Chlorpromazine was present above the recommended intake limit.

    Product
    Major ChlorproMAZINE Hydrochloride Tablets, USP, 50 mg, 100 Tablets, (10x10) blister package, Rx Only, Packaged and Distributed by Major Pharmaceuticals, Indianapolis, IN 46268, USA, NDC 0904-7131-61, UPC (01)00309047131617
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0054-2026·2025-10-15

    Glycine for injection recalled across all lots over sterility assurance

    GenoGenix is recalling Glycine for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    Glycine for Injection, all strengths and presentations, GenoGenix LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0089-2026·2025-10-15

    Epithalon injection recalled from one lot for lack of sterility assurance

    GenoGenix is recalling Epithalon for Injection, 20mg, in all presentations from a single lot for lack of assurance of sterility.

    Product
    Epithalon for Injection, 20mg, all presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692 manufactured for Extension Health.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0055-2026·2025-10-15

    L-Arginine for injection recalled across all lots over sterility assurance

    GenoGenix is recalling L-Arginine for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    L-Arginine for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0010-2026·2025-10-15

    Chlorpromazine 25 mg tablets recalled over nitrosamine above recommended intake limit

    Major Pharmaceuticals is recalling 1,256 blister packs of Chlorpromazine Hydrochloride Tablets USP 25 mg because N-Nitroso Desmethyl Chlorpromazine was present above the recommended intake limit.

    Product
    Major ChlorproMAZINE Hydrochloride Tablets, USP, 25 mg, 100 Tablets (10x10) blister package, Rx Only, Packaged and Distributed by Major Pharmaceuticals, Indianapolis, IN 46268, USA, NDC 0904-7130-61, UPC (01)00309047130610
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0031-2026·2025-10-15

    Bladder supplement capsules recalled over Escherichia coli microbial contamination

    Organicare Nature's Science is recalling 15,075 bottles of FemiClear Daily Bladder Strength for microbial contamination with Escherichia coli O7:K1 and E. coli 1303.

    Product
    FemiClear Daily Bladder Strength Dietary Supplement, 28 Count, UPC 817008020684, SKU FEM50060
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0093-2026·2025-10-15

    Retatrutide injection recalled from one lot for lack of sterility assurance

    GenoGenix is recalling Retatrutide for Injection, 60mg/10mL vial, from a single lot for lack of assurance of sterility.

    Product
    Retatrutide for Injection, 60mg / 10mL vial, all presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0082-2026·2025-10-15

    Sterile saline reconstitution solution recalled across all lots over sterility assurance

    GenoGenix is recalling Sterile Saline Reconstitution Solution for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    Sterile Saline Reconstitution Solution for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0065-2026·2025-10-15

    NAD+ injection recalled across all lots for lack of sterility assurance

    GenoGenix is recalling NAD+ injection at 50 mg/mL and 100 mg/mL in 10 mL multi-dose vials, covering all lots within expiry, for lack of assurance of sterility.

    Product
    NAD+ (Nicotinamide adenine dinucleotide), a) 50 mg/mL, b) 100 mg/mL, 10 mL multi-dose vials, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for CELIA Health
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0041-2026·2025-10-15

    Preserved ascorbic acid injection recalled across all lots over sterility assurance

    GenoGenix is recalling preserved Ascorbic Acid (Vitamin C) for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    Ascorbic Acid (Vitamin C) for Injection, Preserved, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0111-2026·2025-10-15

    Dried bean curd recalled for undeclared wheat across three best before dates

    Gansu Zhaofeng Agricultural Development is recalling 42,552 bags of G&L Food Dried Bean Curd distributed in California because of undeclared wheat.

    Product
    G&L Food Dried Bean Curd Net WT 17.6 OZ (500G) INGREDIENTS: Soybean, Water, Magnesium Chloride as Preservative CONTAINS: Soybean 121C was sterilized at high temperature PRODUCT OF CHINA U.S.A. Distributed By: G&L PRODUCE INC 1140 REVERE AVE SAN FRANCISCO CA 94124 UPC…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0075-2026·2025-10-15

    Elite Stack reconstitution solution recalled across all lots over sterility assurance

    GenoGenix is recalling Elite Stack Reconstitution Solution for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    Elite Stack Reconstitution Solution for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for Extension Health and Medical Health Institute (MHI).
    Category
    Drug
    Distribution
    Distributed nationwide

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