Virginia recalls

Fixing screws on the ceiling movement gear of Canon Medical Alphenix INFX-8000V interventional X-ray systems may loosen over time. This can prevent the ceiling arm from moving side-to-side, cause unusual noises from the suspension system, or trigger sensor errors on the equipment.

Fixing screws on the ceiling-mounted arm of certain Canon Medical Alphenix X-ray systems may become loose. This can prevent the arm from moving side to side, cause unusual noise, or trigger error messages. Three units worldwide are affected.

Fixing screws on the ceiling movement gear in Canon Medical's Alphenix INFX-8000F X-ray systems may become loose over time. This can prevent the ceiling arm from moving side to side, cause unusual noises, or trigger sensor errors during procedures.

Fixing screws in the ceiling-mounted arm of Canon Medical's Alphenix INFX-8000C interventional X-ray systems may become loose. This can cause the ceiling arm to stop moving sideways, create unusual noises, or trigger sensor errors during use.

Certain Siemens LUMIOS Q.namix T interventional X-ray systems with software version VB10D-SP02 may fail to flip orthopedic images as intended when using automatic horizontal flip settings. In some cases, this could result in processing an image from a previous patient instead of the current one.

Certain Siemens interventional X-ray systems with software version VB10D-SP02 have a software issue that can cause images to display incorrectly. When the automatic image-flip feature is used, images may not flip as expected, and in some cases, a previous patient's image could appear instead of the current patient's image.

Aju Pharm's AlternatiV+ Screw-In Anchor has been recalled due to reports of device failure. The anchor may break, bend, pull out, or the suture may break during use. Approximately 416 units were distributed in California and Puerto Rico.

Aju Pharm's AlternatiV+ Max Knotless Anchor surgical device has been recalled due to reports of failure, including anchor breakage, bending, and pulling out during use. The issue affects all lots of models 20KPN4751 and 20KPN5501 distributed in California and Puerto Rico.

Aju Pharm's Genesis Push-In Suture Anchor has been recalled due to reports of device failure during use, including the anchor breaking, bending, or pulling out, as well as suture breakage. About 200 units were distributed nationwide in California and Puerto Rico.

Aju Pharm Co., Ltd. is recalling Genesis Knotless Anchor surgical devices due to reports of device failure. The anchor can break, bend, pull out of tissue, the suture can break, or the packaging can break during handling or use.

Aju Pharm Co., Ltd. is recalling Genesis Dual Thread Screw-In Anchor devices (Models 10N47502 and 10N55002) due to reports of failure during use. The anchor may break, bend, pull out, or cause the suture to break.

Aju Pharm Co., Ltd. is recalling Genesis Screw-In Anchor devices due to reports of failure, including anchor breakage, bending, pull-out, suture breakage, and packaging damage. The recall affects models 10B45003, 10B55003, and 10B65003 distributed nationwide in California and Puerto Rico.

Aju Pharm's Fixone Biocomposite Anchor has been recalled due to reports of device failure, including anchor breakage, bending, pulling out, suture breakage, and packaging damage. The recall affects 1,088 units distributed in California and Puerto Rico. No injuries have been reported to date.

Aju Pharm's Fixone Hybrid Anchor, a surgical device, has been recalled due to reports of device failure. Problems include the anchor breaking, bending, or pulling out during use, as well as suture breakage and packaging damage. This affects 233 units distributed in California and Puerto Rico.

Cerapedics recalled PearMatrix P-15 Peptide Enhanced Bone Graft (1.0cc) due to an incorrect expiration date on certain units. The affected lot is 7014819. No injuries have been reported.

Elekta medical linear accelerators used in cancer radiation therapy have a manufacturing defect affecting electrical grounding in certain models and lot codes. The issue could potentially affect the safe operation of these systems. No injuries have been reported to date.

The Broselow Tape, a tool used in pediatric emergency care to determine medication doses based on a child's length and weight, contains dosing errors for three medications: Vecuronium, Flumazenil, and Ketamine. These errors could lead to incorrect doses being given in emergency situations. The affected units have specific lot numbers and are distributed in the US, Canada, Hong Kong, and Singapore.

The Broselow Tape, a tool used in pediatric emergency care to determine correct medication doses based on a child's length and weight, contains dosing errors for three medications: Vecuronium, Flumazenil, and Ketamine. These errors could lead to incorrect doses being given during emergency treatment.

SunMed Holdings is recalling certain Broselow Pediatric Emergency Rainbow Tapes because they contain incorrect dosing information for three medications: Vecuronium, Flumazenil, and Ketamine. These errors could lead to wrong drug doses during pediatric emergency care. This is a serious safety issue affecting emergency departments and medical facilities.

The Broselow Tape, a tool used in pediatric emergencies to calculate medication doses based on a child's length and weight, contains incorrect dosing information for three medications: Vecuronium, Flumazenil, and Ketamine. These errors could lead to wrong doses being given during emergency care. The FDA has classified this as a Class I recall, the most serious category.

Live it Up brand Super Greens dietary supplement powder may be contaminated with Salmonella Typhimurium. The contamination affects specific lot codes beginning with the letter "A" and expiration dates from August 2026 through January 2028. No illnesses have been reported to date.

Live it Up brand Super Greens dietary supplement powder may be contaminated with Salmonella Typhimurium. The contamination affects specific lot codes beginning with the letter "A" and expiration dates from August 2026 through January 2028. No illnesses have been reported so far.

Qunol Extra Strength Turmeric Capsules (1000mg) in 60-count and 120-count bottles have been recalled due to mold contamination in raw materials used to make the product. The contamination was found in material lots produced in July. No injuries have been reported.

Novadoz Pharmaceuticals is recalling specific lots of glycopyrrolate oral solution (1 mg/5 mL) because the medication failed quality testing for impurities and degradation. The affected lots may not meet safety and effectiveness standards. Three lots are involved, with expiration dates between April and May 2027.

Greenstone LLC is recalling methylprednisolone 4 mg Dosepak tablets (Lot #LG7675, expiring November 2026) because the blister foil is oriented incorrectly. This misalignment can make the dosing directions on the foil confusing or unclear, which could lead to taking the wrong dose.

Some bottles of Parodontax Active Gum Health mouthwash (mint, 16.9 FL OZ) may be missing or have illegible lot and expiration date codes. This makes it impossible to know when the product expires. The affected lot is #0665363 with an expiration date of 08/31/2027.

Baxter Healthcare's Sterile Water for Irrigation 250 mL bottles may contain small plastic particles that came loose from the bottle rim and entered the solution. This affects lot G171359 with an expiration date of 05/31/2027. No injuries have been reported.

Scepter B62 fuel containers lack required safety devices to prevent flash fires and have non-child-resistant spouts that can cause burns or poisoning. These red containers with yellow spouts were sold online from August 2024 through May 2025.

Mays Chemical Company of Puerto Rico recalled approximately 46,315 pounds of frozen, raw pork boneless loins because they were imported into the United States without required reinspection. The pork was distributed to restaurants, institutions, and food service establishments in Puerto Rico. No illnesses have been reported.

The buckle on the cargo area bench of these e-bikes can fail to fully latch, which could allow children to fall or shift unsafely during riding. Gazelle USA has received three reports of buckles not latching properly, though no injuries have been reported yet.