Latest Product Recalls Today

Spherical applicators (radiation therapy accessory) failed to meet manufacturing specifications.

Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss.

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on normal heart rate patients, which may distract clinicians away from management of true positive alarms, which could delay treatment; 2) Small and medium size blood pressure cuffs may contain rough edges, may result in skin irritation/redness.

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

Due to out-of-specification, or potential out-of-specification, levels of endotoxins

Potential sterile breach of the pouches in which devices are packaged.

Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss.

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during a treatment session, the user is not notified of the change.

Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss.

Reduced or no recovery of some strains of Neisseria gonorrhoeae.

Subaru of America, Inc. (Subaru) is recalling certain 2026 Crosstrek Hybrid, 2025-2026 Forester Hybrid, Forester, and 2019-2026 Ascent vehicles. These vehicles were manufactured with an incorrect Gross Axle Weight Rating (GAWR) on the certification label. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) 110, "Tire selection and rims." An incorrect GAWR label may lead to an overloaded vehicle, increasing the risk of a crash.

Harbor Freight Tools (HFT) is recalling certain Kenway 12V LED Towing Light Kits with part number 64282, manufactured November 13, 2019 to December 22, 2019, and 12V Submersible Lights with part number 64274, manufactured July 1, 2019 to July 8, 2019. The lights may not illuminate properly. As such, these lights fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 108, "Lamps, Reflective Devices, and Assoc. Equipment." Improper illumination from the towing lights can reduce trailer visibility to other drivers, increasing the risk of a crash.

Southeast Toyota Distributors, LLC (SET) is recalling one 2026 Tundra truck. The current load carrying capacity modification label is incorrect. As such, this vehicle fails to comply with the requirements of Federal Motor Vehicle Safety Standard number 110, "Tire Selection and Rims." An incorrect load carrying capacity modification label may lead to improper loading of the vehicle, increasing the risk of a crash.

This recall involves VEVOR baby loungers. The recalled baby loungers are made of a foam sleeping pad and padded bumpers with a cloth cover and have a ribbon at one end. They were sold in the following colors and prints: snow deer, good night, forest friends (oval), forest friends (backpack), and green.?"VEVOR" is printed on an attached tag on the outside of the baby lounger's cover.

This recall involves Topyond white pool drain port with cover, sold as a Port Replacement Drainer for swimming pools. The plastic unit comes in a cardboard box with "SP-2850V" printed in bold, and a label which reads: "X004F4YG5X, Topyond Pool Drain Port Repl. MADE IN CHINA". Included in the box are stainless steel screws. The Topyond Pool Drain Port measures 9.1 inches by 6.7 inches and has a 2.3-inch opening for connection. There is no labeling or product identification on the product itself.

This recall involves POPOOO Jungle Safari LED Finger Lights. They were sold in sets of 24 multi-colored lights with white fingertip covers. Each finger light has three internal button cell batteries that power projections of the jungle safari characters when activated. "POPOOO" and "LED FINGER LIGHTS" are printed on the product's blue packaging.

This recall involves Junpower CR2032 Batteries (20 pieces) in specific packaging (Packaging model 2023-V3). The product is packaged in a white box labeled "JUNPOWER Household Batteries," with four packs inside, each pack contains five batteries.

This recall involves CVS Health Medicated Hemorrhoidal Wipes. The pain-relieving wipes were sold in boxes of 20 individually wrapped packets of flushable wipes. The CVS Health logo, a yellow heart, "Rapid Pain Relief" and "Medicated Hemorrhoidal Wipes" is printed on the front of the packet and the box.

This recall involves AMASKY Nursing Pillows. The nursing pillows are C-shaped and sold in white with a crocodile pattern as well as other various colors and patterns. "Brand: AMASKY," "Model No.: BXP99/BXP93/BXP94/BXP96/BXP97" and "Batch Number: 202506001" are printed on a label attached to the pillow.

Nissan North America, Inc. (Nissan) is recalling certain 2026 LEAF vehicles. The outer rear seat belt automatic locking retractors (ALR) may deactivate early, which can prevent a child restraint system (CRS) from securing properly. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 208, "Occupant Crash Protection." An improperly secured child restraint system may not restrain an occupant as intended, increasing the risk of injury during a crash.

Kia America, Inc. (Kia) is recalling certain 2022-2024 EV6 and 2024 EV9 vehicles. The high voltage battery cells may contain misaligned electrodes, which can lead to a fire while parked or driving. A fire increases the risk of injury.