Check a product

Ajanta Pharma USA Inc. is recalling fluphenazine hydrochloride 1mg tablets (NDC 27241-255-01) because stability testing at 18 months found organic impurity levels slightly above specification limits. The tablets contained 1.1% of Impurity-A, exceeding the 1.0% specification. No injuries have been reported.

Moderate·FDA·Sep 16, 2026

ImprimisRx NJ LLC is recalling specific lots of Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution used in medical offices because the medication contains lower-than-intended active ingredients. The affected lots may not work as intended for their intended use.

Moderate·FDA·Sep 16, 2026·ImprimisRx

Certain 2022–2027 Rivian R1S and R1T vehicles, and 2027 R2 models, may display a notification on the rearview camera screen when in reverse, blocking the driver's view behind the vehicle. This obstruction can reduce visibility and increase crash risk.

Moderate·NHTSA·Sep 16, 2026·Rivian Automotive, LLC

The connection between the piston rod and rod end in the rear shock absorbers on certain 2024–2026 Rewaco three-wheeled motorcycles may loosen. This can cause a loss of vehicle control and increase the risk of a crash or injury.

Moderate·NHTSA·Sep 16, 2026·Rewaco Spezialfahrzeuge GmbH

So Delicious Dairy Free® Salted Caramel Cluster Non-Dairy Frozen Dessert pints may contain small stones or other hard objects in the cashew pieces. The issue was found through customer complaints. Affected pints have best-by dates on or before April 3, 2028.

Moderate·FDA·Sep 15, 2026·So Delicious

Certain 2026–2027 Grand Design Lineage recreational vehicles come equipped with tires that have a lower speed rating than the vehicle can reach. At higher speeds, these tires may fail, which could cause a crash.

Moderate·NHTSA·Sep 14, 2026

Certain 2025–2026 Micro Bird G5e school buses have a wiring harness that may have been routed incorrectly. A metal bracket can contact and damage the harness, which could cause a loss of drive power and increase crash risk.

Moderate·NHTSA·Sep 11, 2026·Corp. Micro Bird, Inc.

Certain 2025–2026 Micro Bird G5e transit buses have a wiring harness that may have been routed incorrectly. A metal bracket can contact and damage the harness, causing a loss of drive power to the vehicle. This increases the risk of a crash.

Moderate·NHTSA·Sep 11, 2026·Corp. Micro Bird, Inc.

The electrical contactor in certain S-Series and K-Series wheelchair platform lifts may fail, causing the lift to continue moving even when controls are activated to stop it. This can result in injury to a person in the wheelchair.

Moderate·NHTSA·Sep 11, 2026·Farber Specialty Vehicles

The second-row power seats on certain 2026 Hyundai Ioniq 9 vehicles may fail to detect a person in their path. When the seat moves during automatic fold-and-stow or other powered functions, it could trap a child or adult, causing injury.

Moderate·NHTSA·Sep 11, 2026

A software error in the body control module may cause the engine to stall without warning, and can disable exterior lights, warning lights, or the rearview camera. These failures can make it harder to see or be seen while driving, increasing crash risk.

Moderate·NHTSA·Sep 10, 2026

Certain 2027 Salem and Wildwood travel trailers have an exterior griddle that can be stowed while still connected to the LP gas line. If stowed while gas is running, this creates a fire hazard.

Moderate·NHTSA·Sep 10, 2026

Cracks in the rearview camera's microprocessor may prevent the camera image from displaying properly on certain 2019–2022 Lone Star Vans built on Ram ProMaster chassis. A non-functioning rearview camera reduces the driver's view behind the vehicle and increases crash risk.

Moderate·NHTSA·Sep 10, 2026·Forest River Bus, LLC

Certain 2022–2026 Jeep Wagoneer, Grand Wagoneer, Wagoneer L, and Grand Wagoneer L vehicles have roof rack crossbar pivot bolts that may not have been tightened properly during manufacturing. If the bolts loosen, the crossbars can detach and fall onto the road, creating a hazard for other drivers.

Moderate·NHTSA·Sep 10, 2026

Certain Avix TrailTek RT tires (size 35X12.50R20LT) sold by Wheel Pros have an incorrect label on the sidewall that says "Not for Highway Use" when they should be labeled for highway use. This mislabeling creates confusion about whether the tires are safe to drive on roads and increases crash risk.

Moderate·NHTSA·Sep 10, 2026·Wheel Pros, LLC

Certain Chrysler MOPAR roof rack kits have pivot bolts that may not have been tightened properly during manufacturing. The roof rack crossbars can detach while driving, creating a hazard on the road.

Moderate·NHTSA·Sep 10, 2026

Cardinal Health is recalling 12 procedure kits that include BD Urinary Catheter Trays with CliniClean Pericare Wipes. The wipes may be contaminated with a lubricant used during manufacturing. If a contaminated wipe is used on a patient, it may cause localized skin irritation, redness, or mild inflammation. No injuries have been reported.

Moderate·FDA·Sep 9, 202612 products

Fresenius Medical Care is recalling three dialysis acid concentrate products, GRANUFLO, NaturaLyte and Citrasate, after complaints of blue-green discoloration in the product. No injuries have been reported. The products were distributed nationwide in the US and in Mexico.

Moderate·FDA·Sep 9, 20263 products

Specific lots of B Braun's Discofix Four Way Stopcock extension sets have an incorrect expiration date printed on the carton shipper label. This labeling error could affect proper product tracking and usage verification.

Moderate·FDA·Sep 9, 2026

A software issue in the robotic controller of the Medos Velys Enabling Tech Robotic-Assist Station may cause the robotic arm to move unexpectedly during bone preparation or instrument positioning in orthopedic surgery. This affects 29 devices nationwide.

Moderate·FDA·Sep 9, 2026·Medos

Fresenius Medical Care is recalling four 5008X blood tubing set models because the connection between the Arterial Alpha Clip and the main line or pump segment may leak blood during treatment. A leak could cause blood loss and low blood volume. No injuries have been reported.

Moderate·FDA·Sep 9, 20264 products

Boston Scientific is recalling server software that supports its LUX-Dx, LUX-Dx II, and LUX-Dx II+ insertable cardiac monitors. The recall covers three products, one for each region: US, EU, and ANZ. The software can delay notifications of AF Burden Alerts, which are alerts about atrial fibrillation, and a delayed alert may delay clinical review or treatment. No injuries have been reported.

Moderate·FDA·Sep 9, 20263 products

Medline is recalling 13 convenience kits that contain BD ChloraPrep Clear 1mL applicators from specific lots. The applicator packaging may have an open or incomplete seal, so the applicator could be contaminated. Contaminated applicators can cause skin or soft tissue infections, or more serious infections, and no injuries have been reported.

Moderate·FDA·Sep 9, 202613 products

Baxter is recalling two Novum IQ syringe pump models, totaling about 14,605 units. During a Volume/Time (VOT) multi-syringe infusion, a software issue may occur if a syringe runs empty and is replaced while the Volume To Be Infused (VTBI) is still remaining. No injuries have been reported.

Moderate·FDA·Sep 9, 20262 products

Johnson & Johnson is sending updated surgical instructions for HEALON EndoCoat PRO and HEALON DUET PRO II viscoelastic products used in cataract surgery. The new instructions emphasize that if resistance is felt when inserting the cannula, surgeons should stop, withdraw the cannula, and reassess insertion conditions rather than forcing it—to avoid potential injury to the cornea, iris, or Descemet's membrane (a delicate eye structure).

Moderate·FDA·Sep 9, 2026·Johnson & Johnson Surgical Vision

Medline is recalling 16 convenience kit products that contain BD ChloraPrep Clear or FREPP Clear antiseptic applicators. Wrinkles in the paper lidding may extend to the seal, which could break the sterile packaging and allow microbial contamination. No injuries have been reported.

Moderate·FDA·Sep 9, 202616 products

Diagnostica Stago identified a positive drift in quality control (QC) values in one lot of STA Staclot Protein S reagent within the product's stated 4-hour stability period. This drift could affect the accuracy of test results performed during that window. The issue affects reagent Lot 273074 distributed nationwide.

Moderate·FDA·Sep 9, 2026

Medicom is recalling specific lots of Ritmed Neurological Sponges (non-sterile models 55992C to 55998C) because their endotoxin levels may vary unexpectedly. AVID Medical is recalling three groups of Halyard medical convenience kits that contain these sponges, about 28,800 kits in total. No injuries have been reported.

Moderate·FDA·Sep 9, 20263 products

Philips is recalling four CT scanner product lines, covering 4 product groups, because an unintended radiation issue could affect how the equipment performs. The recall covers Philips Brilliance, IQon Spectral CT, Ingenuity CT, and Brilliance CT 64 systems distributed in the US and US territories. No injuries have been reported.

Moderate·FDA·Sep 9, 20264 products

Ukrop's Homestyle Foods is recalling two sizes of Ukrop's Bread Pudding with Vanilla Sauce, a 13.8 oz single-serve product and a 4 lb kit, because they may contain small metal fragments. The products were shipped to stores in Kentucky, North Carolina, Virginia and West Virginia. No injuries have been reported.

Moderate·FDA·Sep 9, 2026·Ukrop's2 products