Virginia recalls

Sold nationwide. Prestige Consumer Healthcare is recalling 2 products, both Clear Eyes Redness Relief lubricant and redness reliever eye drops in 0.5 fl oz (15 mL) bottles, one sold with a hang tag. The company cannot assure the drops are sterile. No injuries have been reported, and about 2.4 million bottles were affected.

Moderate·FDA·Sep 30, 2026·Prestige Consumer Healthcare2 products

Sold nationwide. Some prefilled pens of Amneal Exenatide Injection may contain no medication due to a defective delivery system. This affects lot AP250095A (expiration 2/28/2027). Patients relying on these pens may not receive their intended dose.

Moderate·FDA·Sep 30, 2026·Amneal Pharmaceuticals

Sold nationwide. Macleods Pharmaceuticals has recalled Olanzapine Tablets USP 5 mg (lot BOB22321A, expiring 07-31-2027) because testing found organic impurities above acceptable limits. The affected bottles were distributed nationwide. No injuries have been reported.

Moderate·FDA·Sep 30, 2026·MacLeods Pharma

Sold nationwide. The FDA has announced a nationwide recall of 9 lubricant eye drops and one eye ointment sold under the Walgreens, AvKare, Reliable-1 Laboratories, TRP Gentle Eyes, Major LubriFresh P.M. and Cameron Pharmaceuticals names. The manufacturer could not confirm that the products are sterile, which is required for eye products. No injuries have been reported.

Moderate·FDA·Sep 30, 2026·Sterling Pharmaceutical Services9 products

Sold nationwide. ICU Medical's 0.9% Sodium Chloride Injection (100 mL) may be mislabeled. Some bags marked as sodium chloride may actually contain potassium chloride instead. This mix-up affects lot 1042188, expiring 10/31/2027, distributed nationwide.

Serious·FDA·Sep 30, 2026·ICU Medical

Unilever's Almond Joy Ice Cream Bars (2.0 fl. oz.) have inaccurate Nutrition Facts information printed on the packaging. The affected products are 6-bar cartons distributed across the United States. No injuries have been reported.

FDA·Sep 30, 2026·Almond Joy

Sold nationwide. A specific lot of Mezzetta Golden Greek Peperoncini Medium Heat (32 oz.) may contain a pest contaminant in the jar. The company identified the issue after a consumer video circulated on social media and immediately launched a voluntary recall of the affected lot. No illnesses or injuries have been reported.

Moderate·FDA·Sep 26, 2026·Mezzetta

Sempio Food Services Inc. recalled approximately 4,596 pounds of ready-to-eat chicken stew products imported from South Korea because they were not properly re-inspected upon entry into the United States. The products were produced on March 30, 2026, and have a best-by date of September 29, 2027. No illnesses or injuries have been reported.

Serious·USDA·Sep 25, 2026·Sempio

Sold nationwide. ABC Trading's light-up toys (ties, headbands, and glasses) contain button cell batteries in compartments that children can easily open. Swallowing these batteries can cause serious internal injuries, chemical burns, and death.

Serious·CPSC·Sep 24, 2026·ABC Trading

Sold nationwide. Love To Dream portable sleep machines contain a lithium-ion battery that can overheat if an incompatible charger is used. This overheating poses a risk of fire or burns.

Moderate·CPSC·Sep 24, 2026·Love To Dream

Sold nationwide. The left temple of INMO Air3 Smart Glasses can overheat during extended use, causing burns to the face and ear. The company has received 10 reports of overheating, including burning sensations. The affected glasses were sold online between December 2025 and August 2026.

Serious·CPSC·Sep 24, 2026·INMO

Sold nationwide. Style Homeware Emerspring mattresses sold on Amazon do not meet federal flammability standards for mattresses. This poses a risk of serious injury or death if a fire occurs near the mattress.

Serious·CPSC·Sep 24, 2026·Style Homeware

Sold nationwide. These wooden dressers can tip over if not anchored to the wall, creating a serious injury or death risk for children. The dressers don't meet federal safety standards for furniture stability.

Serious·CPSC·Sep 24, 2026·Keben

Sold nationwide. Xinan Home WinxMatrs twin-size mattresses do not meet federal flammability standards and pose a risk of serious injury or death from fire. The black, 10-inch-thick mattresses were sold compressed in boxes on Amazon from August through November 2025.

Serious·CPSC·Sep 24, 2026·Xinan Home

Sold nationwide. NEWDERY power banks with model number ZHX-PB22 (black with yellow cables) can have lithium-ion batteries that unexpectedly explode or catch fire. The company has received nine reports of fires, including one that caused $2 million in property damage and one burn injury.

Serious·CPSC·Sep 24, 2026·NEWDERY

Sold nationwide. The lithium-ion battery packs in Blue Cactus Company Reclining Chair model RWX-RBP02 can overheat and catch fire or cause burns. About 51,000 units were sold on Amazon between May 2023 and July 2026. The company has received four reports of batteries overheating, smoking, or igniting.

Serious·CPSC·Sep 24, 2026·The Blue Cactus

Sold nationwide. 5Color size-small bicycle helmets in children's helmet and pads sets do not meet mandatory federal safety standards. The helmets may fail to protect a child's head in a crash, creating a serious risk of injury.

Serious·CPSC·Sep 24, 2026·5Color

Sold nationwide. Kesyup-branded mattresses sold on Amazon do not meet mandatory U.S. flammability standards for mattresses. The mattresses are 12 inches thick, available in twin, full, queen, and king sizes, and have a white top with blue sides and trim. They were sold in compressed boxes from December 2024 through April 2026.

Serious·CPSC·Sep 24, 2026·ZCK01

Sold nationwide. Pi-Cardia Inc. identified a weld issue in the ShortCut transfemoral catheter that may cause the positioning arm to detach during use. The defect affects 46 units in specific serial number lots distributed across eight U.S. states. No injuries have been reported to date.

Moderate·FDA·Sep 23, 2026·PI Cardia

Sold nationwide. ICU Medical's CADD Yellow Medication Cassette Reservoirs may leak medication at the connection point between the luer connector and tubing. This leakage could delay or stop medication delivery, reduce the amount of medication received, expose patients to contamination, or allow air to enter the bloodstream.

Serious·FDA·Sep 23, 2026·ICU Medical

Sold nationwide. Reign Medical's Clench Staple System (Compression) was distributed without adequate performance testing and requires additional FDA clearance. The device is used in bone fixation procedures. About 600 units were distributed nationwide.

Moderate·FDA·Sep 23, 2026·Foundation Medicine

Sold nationwide. Medline is recalling four convenience kit products because some kits may have open seals in their sterile pouch packaging. An open seal may compromise sterility, which could lead to contamination of a sterile field or patient infection if the kit is used. The recall covers 1,196 affected units distributed nationwide, with distribution listed in Arkansas, Florida, North Carolina, Maryland, and Texas.

Moderate·FDA·Sep 23, 2026·Medline4 products

Sold nationwide. Howmedica Osteonics is recalling 12 orthopaedic implant components made from polyethylene material that was aged more than five years before use. The aged material may oxidize, which can increase wear and lead to wear debris, fractured or dislodged parts, and may require revision surgery. No injuries have been reported.

Moderate·FDA·Sep 23, 2026·Howmedica Osteonics12 products

Sold nationwide. The tension bolt in certain Mirion Captus 4000e thyroid imaging systems can fail, allowing the spring arm to unexpectedly drop to its lowest position, about 25 inches from the ground. This affects specific models shipped between April 2019 and February 2024 that have not yet received the redesigned arm. No injuries have been reported.

Moderate·FDA·Sep 23, 2026·Mirion Technologies

Sold nationwide. Datex-Ohmeda is recalling four anesthesia system products, with 1,032 units affected. Certain gas mixer assemblies can automatically switch the system to Alternate O2 control, which delivers 100% oxygen and interrupts anesthetic agent delivery until a clinician intervenes. If that does not happen, the patient may experience decreased anesthetic effect. No injuries have been reported.

Serious·FDA·Sep 23, 2026·Datex-Ohmeda4 products

Sold nationwide. Certain power adapters used with the StoneSmart Connect Console may have higher-than-expected electrical resistance in the grounding path. These adapters may fail electrical safety testing during installation, which could affect device safety.

Moderate·FDA·Sep 23, 2026·Boston Scientific

Sold nationwide. Stryker is recalling six Ethicon XCEL bladeless trocar products, which are reusable surgical access port systems. The ports may crack or separate during use. No injuries have been reported.

Moderate·FDA·Sep 23, 2026·Stryker6 products

Sold nationwide. Blood culture collection kits made by Medical Action Industries contain BD ChloraPrep applicators with potentially open or incomplete seals on their packaging. This compromised seal may allow contamination, and use of affected applicators could result in localized skin or soft tissue infection.

Moderate·FDA·Sep 23, 2026·Medical Action Industries

Sold nationwide. Embecta is recalling two lines of pen needles that were labeled 'For Investigational Use Only' but were sent out as regular commercially sold devices. The recall covers 7,300 units across two products, shipped nationwide to 22 states. No injuries have been reported.

Moderate·FDA·Sep 23, 2026·Embecta2 products

Sold nationwide. Two Kinos Axiom Total Ankle System units were packaged with incorrect patient-specific cutting guides. Using the wrong guides during surgery could lead to poor implant alignment, loose implants, or the need for revision surgery.

Moderate·FDA·Sep 23, 2026·Restor3d