Archive
804 recalls were announced in October 2025.
Of the 804 recalls this month scored against our rubric, 22% are Critical, 10% are Severe.
Which agencies issued them
Glenmark is recalling 26,928 packs of Viorele desogestrel and ethinyl estradiol tablets from one batch after the product failed impurities and degradation specifications.
Endo USA is recalling 1,041 cartons of Everolimus tablets 5mg after the lot returned an out-of-specification result for impurity IP-C.
Ascend Laboratories is recalling several lots of Atorvastatin Calcium Tablets USP 40 mg for failed dissolution specifications.
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.
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.
Ascend Laboratories is recalling several lots of Atorvastatin Calcium Tablets USP 80 mg for failed dissolution specifications.
Tropicana Brands Group is recalling 1,599 cases of Dole Apple Juice in 15.2 fl oz bottles after a manufacturing process deviation that may cause spoilage or microbial contamination.
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.
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.
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.
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.
Forest River is recalling 2025-2026 Alta travel trailers because incorrect axle capacity labels may cause miscalculated weight ratings, increasing crash risk.
Alloy Custom Products is recalling 2023-2025 ACP cryogenic tank trailers because improperly welded suspension towers may cause axle detachment and increase crash risk.
M.C.I. Foods is recalling approximately 91,585 pounds of frozen breakfast burritos and wraps due to possible Listeria monocytogenes contamination.
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.
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.
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.
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.
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.
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.
About 1,860 Vaast A/1 bicycles and framesets are being recalled after 22 reports of frame fractures and three of tube separation, one causing a minor injury in a fall.
About 750 RH Byron travertine and marble tables and desks are being recalled because they can collapse; one dining table collapse has caused lacerations.
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.
Alexis Fire Equipment is recalling 22 fire trucks because a door latch defect may prevent the cab door from opening, potentially trapping occupants.
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.
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.
About 280 Belivium baby loungers are being recalled because low sides, an over-thick sleeping pad and oversized foot openings create an unsafe infant sleeping environment.
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.
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.
About 76,500 WLIVE fabric 12-drawer dressers are being recalled because they are unstable when not anchored to a wall; one tip-over has been reported with no injuries.
About 700 AOWOS 12-drawer dressers sold on Walmart.com are being recalled because they are unstable when not anchored to a wall and violate the STURDY Act standard.
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.
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.
About 1,100 Wilteexs bioethanol fuel bottles are being recalled because they lack the flame mitigation devices required by the Portable Fuel Container Safety Act.
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.
Nate's Fine Foods is recalling 56 cases of frozen cooked fettuccine pasta, totaling 1,680 lbs, for potential contamination with Listeria monocytogenes.
Abiomed is recalling 10,153 Automated Impella Controllers over potential cybersecurity vulnerabilities related to the controller's operating system.
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.
Nate's Fine Foods is recalling 846 cases of Taylor Farms cooked trotolle, totaling 18,612 lbs, for potential contamination with Listeria monocytogenes.
Nate's Fine Foods is recalling 1,357 cases of MAP cooked fettuccine pasta, totaling 40,710 lbs, for potential contamination with Listeria monocytogenes.
Lee K of NY is recalling 43 containers of Pinocchio Catering Aged Kimchi Mackerel because the product contains undeclared milk and shrimp.
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.
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.
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.
New Age International is recalling 175 boxes of Signature brand Enoki Mushroom because the product may be contaminated with Listeria monocytogenes.
Nate's Fine Foods is recalling 261 cases of Taylor Farms cooked farfalle, totaling 6,264 lbs, for potential contamination with Listeria monocytogenes.
Nate's Fine Foods is recalling 52 totes of cooked linguine pasta, totaling 73,050 lbs, for potential contamination with Listeria monocytogenes.
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.
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.
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.
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.
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.
Nate's Fine Foods is recalling 383 cases of Taylor Farms cooked rotini, totaling 9,192 lbs, for potential contamination with Listeria monocytogenes.
Nate's Fine Foods is recalling 972 cases of cooked linguine pasta, totaling 29,160 lbs, for potential contamination with Listeria monocytogenes.
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.
International is recalling 2026 IC Bus CESB school buses because a transmission shift actuator may not be calibrated properly, preventing reverse gear engagement.
Demers Food Group is recalling 966 cases of Scott & Jon's Honey Sesame Salmon Rice Bowl because the product contains undeclared wheat.
GenoGenix is recalling Biotin for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
GenoGenix is recalling B12 Hydroxocobalamin for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
New Spirit Naturals is recalling 37 containers of Ultra Whey Protein Powder because the product contains undeclared milk.
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.
International is recalling 2026 MV commercial trucks because a transmission shift actuator may not be calibrated properly, preventing the vehicle from shifting into reverse.
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.
CorNeat Vision is recalling 180 EverPatch+ units after reviewed complaints identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.
Applied Medical Technology is recalling 1,780 NutraGlide 5 F - 6 F x 55 nasal feeding tubes whose distal tips may detach at lower than expected forces.
Applied Medical Technology is recalling 200 NutraGlide 5 F - 8 F nasal feeding tubes whose distal tips may detach at lower than expected forces.
GenoGenix is recalling Cerebrolysin for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
GenoGenix is recalling Sermorelin lyophilized powder for reconstitution, 10mg in a 10 mL multi-dose vial, from a single lot for lack of assurance of sterility.
GenoGenix is recalling B6 (Pyridoxine HCl) for Injections in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
GenoGenix is recalling L-Carnitine for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
GenoGenix is recalling Thymosin Beta-4 (TB4) for Injection, 15mg, in all presentations from a single lot for lack of assurance of sterility.
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.
GenoGenix is recalling L-Arginine HCl for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
GenoGenix is recalling Oxytocin for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
GenoGenix is recalling Semaglutide for Injection, 20 mg in 10 mL multi-dose vials, from two lots for lack of assurance of sterility.
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.
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.
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.
Egress Capital Partners is recalling 3,547 cases of Taproom Gourmet 15 lb bulk Madison Mix because the product has no ingredient label and contains undeclared peanuts, almonds, wheat and soy.
GenoGenix is recalling GHK-Cu (Copper Peptide) for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
GenoGenix is recalling Lysine for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
GenoGenix is recalling Glycine for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Applied Medical Technology is recalling 390 NutraGlide nasal feeding tubes whose distal tips may detach at lower than expected forces.
GenoGenix is recalling Elite Stack MSC Exosome Reconstitution Solution for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
GenoGenix is recalling Proline for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
GenoGenix is recalling Magnesium Chloride for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of 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.
GenoGenix is recalling Vitamin D3 for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
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.
ImaCor is recalling 45 ClariTEE miniaturized TEE probes after a production assembly error left articulation reversed, so moving the lever forward anteflexed the tip instead of retroflexing it.
El Rojo Wholesale is recalling 2,904 units of El Rojo Pasta De Harina wheat pellets because the pack has no ingredient list, leaving wheat and Yellow No. 6 undeclared.
GenoGenix is recalling Lipo MIC + B12 Methylcobalamin for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Canon Medical Systems is recalling eight radiography/fluoroscopy systems because changing the acquisition program returns the collimator to a default ROI, leaving the X-ray area partially covered by a static image.
GenoGenix is recalling Bacteriostatic Water for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
GenoGenix is recalling Glutathione Magnesium for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
GenoGenix is recalling Lipo MIC + L-Carnitine for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
GenoGenix is recalling Reconstitution XO Solution for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
GenoGenix is recalling Tirzepatide 60mg/10 mL for Injection from two lots for lack of assurance of sterility.
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.
GenoGenix is recalling B-Complex for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
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