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
GenoGenix is recalling Methylene Blue for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Acuity Specialty Products is recalling Wyandotte Sanifect E3 ethanol-based hand sanitizer because required receipt testing of incoming alcohol was not performed, so methanol risk could not be excluded.
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 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 Semaglutide for Injection, 20 mg in 10 mL multi-dose vials, from two lots for lack of assurance of sterility.
Egress Capital Partners is recalling 3,547 cases of Taproom Gourmet 20 lb bulk Park Mix because the product has no ingredient label and contains six undeclared allergens.
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.
GenoGenix is recalling B12 Hydroxocobalamin for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
FUJIFILM is recalling 16 FDR Visionary Suite systems because the shaft mounting the X-ray tube unit on the support may break, with protective parts possibly not working.
Major Pharmaceuticals is recalling 1,394 blister packs of Chlorpromazine Hydrochloride Tablets USP 200 mg because N-Nitroso Desmethyl Chlorpromazine was present above the recommended intake limit.
GenoGenix is recalling GAC for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
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 Alpha Lipoic Acid 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 L-Glutamine 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.
Egress Capital Partners is recalling 3,547 cases of Taproom Gourmet bulk Fifth Avenue Mix because the product has no ingredient label and contains undeclared peanuts, almonds, cashew and soy.
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.
GenoGenix is recalling Amino Blend for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
GenoGenix is recalling N-Acetyl-L-Cysteine for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
GenoGenix is recalling BPC-157 for Injection, 15mg/10mL vial, from a single lot 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 Tri-Immune for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
RC Outsourcing is recalling 2,669 prefilled Bevacizumab 1.75 mg/0.07 mL intravitreal syringes for lack of assurance of sterility.
GenoGenix is recalling CoQ10 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.
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.
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.
New Spirit Naturals is recalling 83 containers of Gluta Plus (Glutathione) capsules because the product contains undeclared milk.
New Spirit Naturals is recalling 79 containers of Meal In A Glass protein powder in vanilla, chocolate and strawberry because the product contains undeclared milk.
GenoGenix is recalling Zinc Sulfate for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
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.
Applied Medical Technology is recalling 200 NutraGlide 5 F - 8 F nasal feeding tubes whose distal tips may detach at lower than expected forces.
CorNeat Vision is recalling 630 CorNeat EverPatch units after reviewed complaints identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.
Egress Capital Partners is recalling 3,547 cases of Taproom Gourmet 18 lb bulk Empire Mix because the product has no ingredient label and contains undeclared tree nuts.
GE is recalling 7,302 AW Server systems after identifying a security vulnerability that, if exploited, could compromise the confidentiality, integrity and availability of patient data.
GenoGenix is recalling Glutathione Preserved for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
GenoGenix is recalling B12 Methylcobalamin 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.
Inpeco is recalling eight FlexLab systems because the Sample Integrity Module's hemolysis, icterus and lipemia function has not been evaluated by the FDA.
Sadecki Bartnik is recalling 336 jars of Pylek Kwiatowy bee pollen distributed in Illinois because of detectable pyrrolizidine alkaloids.
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 Proline for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
GenoGenix is recalling Ultra Burn for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
GenoGenix is recalling EDTA for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
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.
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 Thymosin Beta-4 (TB4) for Injection, 15mg, in all presentations from a single lot for lack of assurance of sterility.
GenoGenix is recalling combined BPC-157/Thymosin Beta-4 for Injection across three lots for lack of assurance of sterility.
GenoGenix is recalling L-Arginine HCl for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.
Accord Healthcare is recalling 54,432 bottles of Levothyroxine Sodium Tablets USP 88 mcg after long-term stability testing found assay content below the approved specification range.
M.O.M Enterprises is recalling 46,752 bottles of Organic Baby Bedtime Drops across three lots for potential yeast contamination.
B. Braun is recalling 2,760 PERIFIX FX Continuous Epidural Anesthesia Trays, product code CE17TKFS, because the lid of the catheter connector may be in the incorrect position.
B. Braun is recalling 2,450 Design Options Pain Management Trays because the lid of the catheter connector may be in the incorrect position.
B. Braun is recalling PERIFIX FX Continuous Epidural Anesthesia Trays, product code CE17TKFSDT, because the lid of the catheter connector may be in the incorrect position.
Beckman Coulter is recalling 2,146 units of SYNCHRON Systems Phosphorus reagent because specific lots may fail calibration before the lot expiration date, delaying patient results.
Fresenius Medical Care is issuing a recall covering Optiflux High Flux E-beam Dialyzers to tell users that the caps changed from threaded to press-on and must be pressed firmly to affix.
B. Braun is recalling 2,840 Combined Spinal and Epidural Anesthesia Trays, product code NES1727KFX, because the lid of the catheter connector may be in the incorrect position.
Eden's Elixirs is recalling 10,000 Eskay Brands mint flavored chewable tablets distributed in Texas because Yellow #5 is not declared.
B. Braun is recalling PERIFIX FX Continuous Epidural Anesthesia Trays, product code CE17TKF, because the lid of the catheter connector may be in the incorrect position.
B. Braun is recalling 5,770 Design Options PERIFIX FX Epidural Anesthesia Trays because the lid of the catheter connector may be in the incorrect position.
Eden's Elixirs is recalling 284,354 Lifted Made-Lemon chewable tablets distributed in Texas because Yellow #5 is not declared.
B. Braun is recalling 21,270 PERIFIX FX Continuous Epidural Anesthesia Trays because the lid of the catheter connector may be in the incorrect position.
B. Braun is recalling 60 Combined Spinal and Epidural Anesthesia Tray 2 units because the lid of the catheter connector may be in the incorrect position.
B. Braun is recalling PERIFIX FX Continuous Epidural Anesthesia Trays, product code CE17TKFCPS, because the lid of the catheter connector may be in the incorrect position.
Acella Pharmaceuticals is recalling 4,680 five-hundred-count bottles of Doxycycline Hyclate Tablets USP 100 mg after stability testing found the lot did not meet dissolution specifications.
LeMaitre Vascular is recalling 10 Artegraft Collagen Vascular Grafts distributed with an incorrect label lacking CE and UKCA marks and without the patient leaflet and implant card.
B. Braun is recalling 48,110 PERIFIX FX Continuous Epidural Anesthesia Trays, product code CE17TKFC, because the lid of the catheter connector may be in the incorrect position.
B. Braun is recalling 10,130 ESPOCAN Combined Spinal and Epidural Anesthesia Trays because the lid of the catheter connector may be in the incorrect position.
Dr. Reddy's is recalling 571 vials of Succinylcholine Chloride Injection USP after an out-of-specification result for decreased preservative concentration at six-month stability testing.
Eden's Elixirs is recalling 141,000 Lifted Made-Mint chewable tablets distributed in Texas because Yellow #5 is not declared.
B. Braun is recalling PERIFIX FX Continuous Epidural Anesthesia Trays, product code CE17TBFC, because the lid of the catheter connector may be in the incorrect position.
B. Braun is recalling PERIFIX FX Continuous Epidural Anesthesia Sets, product code CE17TFC, because the lid of the catheter connector may be in the incorrect position.
Chrysler is recalling specific Mopar Fuel Delivery Modules because the fuel pump may fail, causing a loss of drive power and increasing crash risk.
Nova Bus is recalling 2019-2020 LFS commercial buses because driver's door windows may lack the required DOT code mark, potentially leading to incorrect glass replacement and reduced visibility.
Tesla is recalling certain 2024-2026 Cybertruck vehicles running software before 2025.38.3 because the front parking lights may be too bright and exceed the maximum permitted light output.
Toyo is recalling specific off-road and all-terrain tires because production contamination may cause tread separation, increasing the risk of vehicle instability and crashes.
Ford is recalling specific 2015-2020 models because the rearview camera may display a distorted or blank image, increasing crash risk.
Ford is recalling 1,412 Explorer and Lincoln Aviator vehicles because the trailer hitch assembly bolts may be loose, risking loss of control or trailer detachment while towing.
Daimler Trucks North America is recalling 2026 Thomas Built SAF-T-LINER HDX2 school buses because rear exterior joints may have insufficient strength, failing federal safety standards.
Forest River is recalling 20,305 travel trailers because the distribution panel wire may be connected to the battery without over current protection.
Ford is recalling 2020 Escape vehicles because incorrectly manufactured rear brake pads may reduce braking performance during a booster malfunction, increasing crash risk.
Tesla is recalling 12,963 vehicles because the battery pack contactors may fail, causing a loss of drive power.
Supreme is recalling 2025 Wabash insulated truck bodies because misaligned bolts may allow the auxiliary battery box to detach, creating a road hazard.
Ford is recalling 2025 Bronco and Ranger vehicles because the windshield may not be properly bonded, posing an injury risk in a crash.
Ford is recalling 2,101 Mustangs that were repaired incorrectly under an earlier recall, because the brake fluid level sensor may not activate the low-fluid warning indicator.
Ford is recalling 59,006 vehicles across many Ford and Lincoln lines because the engine block heater may crack and leak coolant, short circuiting when plugged in.
Ford is recalling aftermarket supercharger kits for 2024-2025 Mustangs because a software error may disable safety features, increasing crash risk.
Forest River is recalling eight 2026 Flagstaff and Rockwood trailers whose waste water holding tank ventilation pipe may not be terminated outside the vehicle.
Ford is recalling certain engine block heaters for 2023-2026 vehicles because they may overheat and cause a fire. Dealers will replace the heater element and inspect the cord.
Ford is recalling 291,901 Super Duty trucks because the 360-degree view camera system may not display a rearview image properly in certain lighting conditions.
Ford is recalling specific engine block heaters that may crack and leak coolant, causing a short circuit and increasing fire risk.
Brenner Tank is recalling 2026 TKQXFR tank trailers because an incorrect emergency valve may leak hazardous liquids during a crash.
Ford is recalling 84 Lincoln Corsair vehicles because water may leak into the rear combination lights, potentially killing the reverse, tail, brake or turn signal function.
Ford is recalling 2024-2026 Lincoln Nautilus Hybrids and 2025 Explorer Hybrid police vehicles because a software error may prevent the pedestrian warning sound from playing.
About 25,030 EcoFlow Delta Max 2000 power stations are being recalled after six reports of the units catching fire, with property damage totaling over $850,000.
About 48,000 Living Glow five-in-one portable waist fans are being recalled because the lithium-ion batteries can overheat while charging; four fans have melted or caught fire.
About 46,660 Ambiano electric pressure cookers sold at ALDI are being recalled because the lid can be opened before pressure is released; 11 incidents include eight severe burn injuries.
About 19,500 more ESR HaloLock wireless power banks are being recalled after 20 reports of the lithium-ion battery catching fire and exploding, with about $30,000 in property damage.
Braun Industries is recalling 2023-2026 ambulances because a damaged brake pedal switch may prevent cruise control from disengaging, increasing crash risk.
Looking for a different month? Back to 2025.