Archive
525 recalls were announced in September 2025.
Of the 525 recalls this month scored against our rubric, 13% are Critical, 10% are Severe.
Which agencies issued them
Volvo is recalling certain 2025 EX90 vehicles because a spindle nut may detach from the power operated tailgate drive units, causing the tailgate to drop suddenly. Owners are told not to use the feature.
Thor Motor Coach is recalling certain 2024-2025 Luminate and Indigo RVs because the LP tank support tube may be too short with an insufficient weld that can fracture, allowing the tank to detach.
Q'Straint is recalling QRT-Deluxe and QRT-Max wheelchair restraints because the retractors may not lock, preventing the wheelchair from being properly secured.
Nissan is recalling certain 2021-2022 Leaf vehicles with Level 3 quick charging capability because the lithium-ion battery may overheat during fast charging, increasing fire risk. Owners should not use Level 3 charging until a free software update becomes available.
Hillshire Brands is recalling corn dog and sausage on a stick products nationwide due to possible wood contamination. Consumers should discard or return the affected items.
Medix Specialty Vehicles is recalling Phoenix Quick Liner Wheel Covers on Ford Type-III ambulances because they may detach during transit, creating a road hazard.
International is recalling 2025-2026 IC Bus CECB commercial buses because a tire may damage an air line, causing the parking brake to activate unintentionally while driving.
About 1,290,000 Oster French Door Countertop Ovens are recalled because the doors can unexpectedly close. Sunbeam has 95 reports of doors closing and causing burns, including two second-degree burns.
International is recalling certain 2024-2026 IC Bus CESB school buses because a tire may contact and damage the air dryer discharge line, causing an air leak that unintentionally applies the parking brake.
USDA FSIS issued a public health alert for specific ready-to-eat pasta meals sold at Walmart and Trader Joe's due to possible Listeria monocytogenes contamination linked to a confirmed outbreak.
Bentley is recalling certain 2025-2026 Continental GT, Continental GTC and 2025 Flying Spur vehicles because the bolted joint securing the high-pressure fuel pump to the V8 engine may be improperly tightened.
About 20,000 Hoovy Cooling Gel Insert Pads for car seats and strollers are recalled because they can become hot in the sun or a hot car. One child suffered second degree burns requiring medical attention.
Cognito Motorsports is recalling 12,160 Rev C Ball Joints installed on 2011-2025 GMC and Chevrolet 2500HD and 3500HD trucks because the ball stud may pull through the housing, risking loss of steering.
Chrysler is recalling certain 2022-2024 Jeep Wagoneer and Grand Wagoneer vehicles because the quarter trim on the driver and passenger windows may not have been properly secured and can detach.
Altec is recalling 2024-2025 A-Class vehicles because platform retaining plate bolts may not have been properly tightened, posing a risk of detachment and injury.
BMW is recalling specific 2019-2025 models because the starter motor may overheat and ignite nearby combustible material, increasing the risk of a fire.
BMW is recalling 2026 M4 and 430i vehicles because improperly connected battery cables may cause engine stalls or fires.
About 133,000 Persilux zebra blinds are recalled because long operating cords pose strangulation and entanglement hazards to children, violating the federal window covering rule. No incidents reported.
About 28,000 RELIEVE numbing cream containers are recalled because the lidocaine product is not in child-resistant packaging as required by the Poison Prevention Packaging Act. No incidents reported.
Kia is recalling certain 2021-2023 Sorento vehicles because the heating, ventilation and air conditioning blower motor wiring harness may be inadequate, which can result in a fire.
Evenflo is recalling Gold Revolve360 Slim and Revolve360 Slim child seats because loose headrest foam can break off and pose a choking hazard to children.
Land Rover is recalling certain 2023 Range Rover Evoque vehicles because water may enter the rearview camera, so the image may not appear on the display or may appear distorted.
International Motors is recalling 2026 IC Bus CESB school buses because a weld failure may prevent the left-side wiper from working, increasing crash risk.
International is recalling 2026 IC Bus CECB commercial buses because a weld on the wiper crank shaft may fail, causing the left-side wiper to stop working.
Chrysler is recalling Mopar rear quarter glass window assemblies because the trim may not be properly secured. Detached trim can create a road hazard for other vehicles.
About 550 Autoez bamboo shades are recalled because long operating cords and accessible inner cords pose strangulation and entanglement hazards to children. No incidents reported.
Altec is recalling 2021-2025 aerial devices because the outrigger pad holder may be installed too close to the exhaust, increasing fire risk.
General Motors is recalling certain 2024 Chevrolet Equinox EV vehicles because the pedestrian alert sound system may not change volume enough between standstill and low speed, failing FMVSS 141.
Piccolo Pranzo Box, 14.5 oz, from Fresh and Ready Foods is recalled for undeclared wheat and milk. The FDA classified the action as Class I. 233 units are affected.
Honey Balsamic dressing in 3.4 ounce plastic pouches is recalled because it contains undeclared soy and sesame. The FDA classified the action as Class I. 46,800 units are affected.
Vegetable Tray Cucumbers in 3/2 lb cardboard boxes are recalled because the product is contaminated with Salmonella. The FDA classified the action as Class I.
Unichem Cyclobenzaprine Hydrochloride Tablets, 10 mg, lot GMML24026A, are recalled because bottles labeled as cyclobenzaprine contained yellow Meloxicam 7.5 mg tablets. The FDA classified the action as Class I.
Cucumbers Peeled/Diced 1/4 inch KBS in 5 lb cardboard boxes are recalled because the product is contaminated with Salmonella. The FDA classified the action as Class I.
Sliced Cucumber, 8 oz, sold in cardboard boxes, is recalled because the product is contaminated with Salmonella. The FDA classified the action as Class I. 89 boxes are affected.
3M Ranger Blood/Fluid Warming High Flow Sets are the subject of a field action to clarify flow rates, inlet fluid temperatures and the location of the outlet temperature. The FDA classified it as Class I.
Endico brand Mixed Vegetables, 2.5 lb frozen bags produced 06/17/2025, are recalled because the product may be contaminated with Listeria monocytogenes. The FDA classified the action as Class I.
SmartDrive MX2+ SpeedControl Dials, REF MX2-3DCK, are recalled because a faulty electrical connection between the dial and the wheelchair motor may cause loss of control. 15,834 units are affected.
Chili Crunch Market Mezze, 14.5 oz, from Fresh and Ready Foods is recalled for undeclared wheat. The FDA classified the action as Class I. 233 units are affected.
SmartDrive MX2+ SpeedControl Dials are recalled because a faulty electrical connection between the dial and the wheelchair motor may cause loss of control. The FDA classified the action as Class I. 25,389 units are affected.
SmartDrive MX2+ SpeedControl Dials, REF MX2-3DCMC, are recalled because a faulty electrical connection between the dial and the wheelchair motor may cause loss of control. 8,413 units are affected.
Cucumber Sliced PLD KBS in 2/10 lb cardboard boxes, code X3234937, is recalled because the product is contaminated with Salmonella. The FDA classified the action as Class I.
Endico brand Peas & Carrots, 2.5 lb frozen bags produced 06/11/2025, are recalled because the product may be contaminated with Listeria monocytogenes. The FDA classified the action as Class I.
Spanish Club Ciabatta, 10.5 oz, from Fresh and Ready Foods is recalled for undeclared wheat and milk. The FDA classified the action as Class I. 233 units are affected.
Tuscan Artichoke and Mozzarella Salad, 8.5 oz, from Fresh and Ready Foods is recalled for undeclared wheat and milk. The FDA classified the action as Class I. 233 units are affected.
Cucumber Peeled Sliced KBS in 2/5 lb cardboard boxes, code X3235434, is recalled because the product is contaminated with Salmonella. The FDA classified the action as Class I.
Neuhaus Original Belgian Chocolate popping milk chocolates with cookies, 4.23 oz, are recalled because the product contains undeclared wheat. The FDA classified the action as Class I.
Volkswagen is recalling one Audi SQ7 vehicle because the fasteners securing the high pressure fuel pump may not be tightened properly, resulting in a fuel leak. The vehicle has been repaired.
Volkswagen is recalling certain 2025-2026 GTI, Golf R, Audi A5, S5, A6 and Q4 e-Tron models because the torsion bar in one or both front seat belt retractors may have been damaged during production.
FLEX Monoclonal Mouse Anti-Human CD20cy for Dako Omnis is recalled because of the potential for weak staining, which may result in false negative CD20 identification. 4,145 units are affected.
Charge-Up Chilaquiles, 3.5 oz, lot 52061, is recalled because Yellow #5 and Yellow #6 are undeclared. 566 packages are affected.
Frozen AquaStar Breaded Butterfly Shrimp, clean-tail, in 3 lb packages is recalled because the product may be contaminated with Cesium-137. 126 cases are affected.
UniCel DxH 800 Coulter Cellular Analysis Systems configured with the LED HGB photometer are recalled because they may produce erroneously high hemoglobin results on samples with elevated white blood cell counts.
UniCel DxH 900 Coulter Cellular Analysis Systems configured with the LED HGB photometer are recalled because they may produce erroneously high hemoglobin results on samples with elevated white blood cell counts.
Heartstring III Proximal Seal Systems, model HS-3045, are recalled after three failure modes were identified, including failure of the deployed seal to provide adequate hemostasis. 126 units are affected.
Pinnacle Radiation Therapy Planning System software is recalled because of a potential image error of the Region of Interest for expansion or contraction in head first prone, feet first supine and feet first prone orientations.
BulkSupplements.com Inositol powder, lot 2507803, is recalled because the finished product may be contaminated with pathogenic Staphylococcus aureus. 1,001 units are affected.
AquaStar Cocktail Shrimp with cocktail sauce, 6 oz packages sold at Walmart, is recalled because the product may be contaminated with Cesium-137. 22,500 cases are affected.
Frozen Mercado Kroger Cooked Shrimp pieces, medium peeled tail-off, in 2 lb packages, are recalled because the product may be contaminated with Cesium-137. 18,000 bags are affected.
B. Braun 0.9% Sodium Chloride Irrigation USP, 3000 mL bags, is recalled for lack of assurance of sterility because port misalignment may allow fluid leakage. 16,228 bags are affected.
Fagron Sterile Services bevacizumab (Avastin) Injection, 1.25 mg/0.05 mL single-dose syringes, is recalled nationwide for lack of assurance of sterility. 109,320 syringes are affected.
Best Yet, Arctic Shores and Great American branded frozen cooked shrimp is recalled because it was made under insanitary conditions and may have been contaminated with Cesium-137. 11,081 cases are affected.
Vanilla G. Nutt Ice Cream in pint, quart and half gallon sizes is recalled because it may contain undeclared almond. 12 pints distributed in New York are affected.
Bulk frozen raw half shell oysters, 15 lb, from harvest dates in January 2025 are recalled because the product is potentially contaminated with norovirus. 1,705 cases are affected.
Abdallah Candies Sea Salt Caramel Dark Miniature, item 2237 ML in a 5.20 lb box, is recalled for undeclared peanut and pecan. One box distributed in Pennsylvania is affected.
UniCel DxH 690T Coulter Cellular Analysis Systems configured with the LED HGB photometer are recalled because they may produce erroneously high hemoglobin results on samples with elevated white blood cell counts.
Heartstring III Proximal Seal Systems, 3.8 mm, are recalled after three failure modes were identified, including failure of the deployed seal to provide adequate hemostasis. 28,331 units are affected.
Exactech Equinoxe Reverse Shoulder humeral liners under REF 320-38 and 320-42 are recalled because the articular surface position falls outside the dimensional specification in the labeling. 61,334 units are affected.
B. Braun Sterile Water for Injection USP, 3000 mL bags, is recalled for lack of assurance of sterility because port misalignment may allow fluid leakage. 26,316 bags are affected.
UniCel DxH 600 Coulter Cellular Analysis Systems configured with the LED HGB photometer are recalled because they may produce erroneously high hemoglobin results on samples with elevated white blood cell counts.
SureStep Foley Tray Systems, REF A303414A lot NGJY3685, are recalled because incorrect inserts may lead users to misidentify the catheter material or coating, risking infection or allergic reaction.
Exactech Equinoxe Reverse Shoulder humeral liners in 38 mm and 42 mm sizes are recalled because the articular surface position falls outside the dimensional specification in the labeling. 11,542 units are affected.
The Vercise Deep Brain Stimulation Systems Surgical Implant Manual is being recalled after wire breaks in rechargeable pulse generators implanted in the submuscular pectoral location. 25,260 units are affected.
Sun Pharmaceutical's Kit for the Preparation of Technetium Tc 99m Mertiatide, lot AD70995, is recalled after an out-of-specification result for sulphate in the sodium tartrate dihydrate used in production. 1,870 kits are affected.
FLEX Monoclonal Mouse Anti-Human CD20cy for Dako Omnis, catalog GA60461-2J, is recalled because of the potential for weak staining that may result in false negative CD20 identification. 67 units are affected.
Lippert is recalling specific paddle latches used on REV Recreation Group vehicles because they may lock unintentionally, preventing access to the liquid propane compartment and increasing fire risk.
Zydus Entecavir Tablets, USP, 1 mg, lot E309377, are recalled nationwide after failing impurity and degradation specifications. 4,440 bottles are affected.
SureStep Foley Tray Systems with Bard Lubri-Sil catheters, REF A942216 lot NGJX4320, are recalled because incorrect inserts may lead users to misidentify the catheter material or coating. 3,670 units are affected.
A handheld ultraviolet-C germicidal wand is recalled because it emits an unsafe level of UVC radiation, reaching the Risk Group 3 exposure limit in about 2.2 minutes and risking skin and eye injuries.
Aripiprazole Tablets, USP, 10 mg, lot 24144162, distributed by Ascend Laboratories, are recalled nationwide as a superpotent drug. 2,256 bottles are affected.
Bake-a-holic Cheesecake Royale Pecan Bars are recalled because a label review found milk and dairy absent from the Contains statement and soy removed from the label. 60 cases are affected.
Campsite Lentejas, 4.0 oz, lot 52060, is recalled because Yellow #5 and Yellow #6 are undeclared. 154 packages are affected.
FLEX Monoclonal Mouse Anti-Human CD20cy for Dako Omnis, catalog GA60461-2CN, is recalled because of the potential for weak staining that may result in false negative CD20 identification. 65 units are affected.
Zydus Entecavir Tablets, USP, 0.5 mg, lot E309376, are recalled nationwide after failing impurity and degradation specifications. 4,344 bottles are affected.
Abdallah Candies Cream Caramels, Milk, item 2210L in a 6.26 lb box, are recalled for undeclared peanut and pecan. One box distributed in Pennsylvania is affected.
Sand Bar, Great American and First Street branded frozen raw shrimp in 2 pound bags is recalled because it was made under insanitary conditions and may have been contaminated with Cesium-137.
Heartstring III Proximal Seal Systems, 4.3 mm, are recalled after three failure modes were identified, including failure of the deployed seal to provide adequate hemostasis. 12,471 units are affected.
SureStep Foley Tray Systems, REF A303316A lot NGJX6399, are recalled because incorrect inserts may lead users to misidentify the catheter material or coating, risking infection or allergic reaction.
Hi-Tech Pharmaceuticals Joint-RX dietary supplement, 90 count, lot 503110607, is recalled for unapproved drug claims. The recall covers 85,950 units across the firm's affected products.
VITROS Chemistry Products LAC Slides, catalog 8150112, from coating 0130 and above are recalled because of increased calibration failures on VITROS XT systems, delaying lactate results. 2,320 units are affected.
LG Sciences Battle Hardener Platinum Series complete 6 week cycle with PCT is recalled for unapproved drug claims. The recall covers 85,950 units across the firm's affected products.
Formutech Nutrition Flexible Joint Formula with Cissus Quadrangularis, 240 capsules, lot 405310805, is recalled for unapproved drug claims. The recall covers 85,950 units across the firm's affected products.
i-STAT EG6+ cartridges are recalled across all lots for lack of a 510(k) premarket clearance reflecting updated sample types and measurement ranges. 547,250 units are affected.
Hi-Tech Pharmaceuticals Fish Oil, 90 soft gels, lot 517120551, is recalled for unapproved drug claims. The recall covers 85,950 units across the firm's affected products.
Sulfamethoxazole and Trimethoprim Tablets, USP 800 mg/160 mg double strength, in 6, 10, 14 and 20-count bottles are recalled because a micro-organism was found on a lot of packaging coil.
Hi-Tech Pharmaceuticals Beta Sitosterol, 90 tablets, lot C1847, is recalled for unapproved drug claims and misbranding. The recall covers 85,950 units across the firm's affected products.
PrimeNutrition Taurine, 8.12 oz, lot 710581618, is recalled for unapproved drug claims and misbranding. The recall covers 85,950 units across the firm's affected products.
Frontier Devices 14 mm Distraction Pins in 5 single packs are recalled because the labeling includes a shelf life that has not been validated. 2,700 units are affected.
Frontier Devices 16 mm Distraction Pins in 10 single packs are recalled because the labeling includes a shelf life that has not been validated. 490 units are affected.
i-STAT EG7+ cartridges are recalled across all lots for lack of a 510(k) premarket clearance reflecting updated sample types and measurement ranges. 6,115,950 units are affected.
iForce Nutrition Joint Help dietary supplement, 120 capsules, lot 101330812, is recalled for unapproved drug claims. The recall covers 85,950 units across the firm's affected products.
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